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This is really interesting. I didn't get any tingling from any of theses videos and there were a few videos on YouTube that said they would trigger the sensation too but nothing, although, most of them were extremely annoying and irritating like the whispering ones, they were not pleasant at all :( . I was looking for the reason I get a full body tingling when I hear certain singing voices. Its like a flushing from my feet to my head of tiny bubbles at least I know it isnt called ASMR I looked into Frisson also and it isn't that either..... the search continues.
Finally something to explain my "photocopier man" feeling which has been a standard joke in our family. I first discovered this feeling when I was a teenager working in an office where a repair man would come regularly to maintain the photocopier and I would experience this sensation of well-being while he was working. It was in a fairly small office and usually he would clean the screen with an acetone base cleaner so I always thought that the fumes from that created a mini "high". I have had it at various times usually when there is someone repairing something in the office eg putting data cables, fixing sockets etc. I now work in a research lab and have had it when participants are in another room being tested with senors on their heads and I have no visual or auditory input from them just the sense of them being there. I have had it to a lesser extent from acupuncture and find massage of any kind extremely unpleasant. It's nice to find out that it's not just me that has this strange feeling for no apparent reason.
I'm not sure if I have asmr or not but I've never felt this feeling or some thing similar to this at all but I felt it 8times while playing battlefield hardline today but I know it not from that. When it happens I get a small tingly sensation and it's warm and fuzzey and feels nice but not strong enough to make me really relaxed. I don't know why but when ever I feel this and close my eyes and relax my muscles, it seems to last a little longer then if I move around. I know this isn't frission because I don't get energized by it but it makes me want to sleep.also I have aspergers, ADD and ADHD. I'm not sure if this makes it so I can or can't feel this or not. can some one please reply?
Ad Advertisement Agnieszka Janik McErlean Anxiety Art ASMR asmr-research.org ASMR ad ASMR artist ASMR book ASMR experiences ASMR film ASMR inspired commercial ASMR movie ASMR Research ASMR survey ASMR testimonials ASMRtist ASMR triggers ASMR University ASMR videos Autonomous Sensory Meridian Response Beverley Fredborg Biology Bob Ross Brain Bryson Lochte Celebrities Commercial Data Depression Dissertation Dove Dove chocolate Emma Barratt Film Flow fMRI Graeme Cole Highly Sensitive Person History of ASMR Ilse Blansert Insomnia interview Jennifer Allen Jim Clark Julie Young live ASMR Melatonin Michael Banissy Mike Reed Misophonia Movie Murmurs Musical frisson Neuroscience Neurotransmitters Nick Davis Oxytocin Peer-reviewed PeerJ Pepsi Personality Podcast Polls publication Research Science Sleep Spa Stephen Smith Survey Voices of ASMR WhisperingLife WhispersRed
Kelly knows that she inspires other kids to take up ASMR – children at school ask for advice on how to make popular YouTube videos. At one football game recently, kids swamped Kelly for photos. "It was like… crazy," Kelly whispers dramatically. "I went with friends and we walked past this group of cheerleaders and they all got quiet. They came up one after another and were like, 'Let's take a picture.'"
Smith speculates that ASMR may be similar to synesthesia, the fascinating neurological condition in which people see numbers in color and "taste" shapes. "In synesthesia," he says, "there have been some studies that show there's slightly atypical wiring in the brain that leads to slightly different sensory associations, and I think that may be the same thing we have here."
I have repeatedly tried listening to ASMR YT videos, however, I have found them actually highly irritating and not calming. The whispering (extreme soft speaking) cause me great annoyance. You are right in that not all people respond to ASMR videos in the same manner. However, a back massage with calming music, listening to powerful worship music, dialogue of a spiritual nature, sitting by water and meditation on Scripture are triggers for this sensation.
ASMR can vary from person to person because it's all about perception, licensed clinical psychologist John Mayer, Ph.D., author of Family Fit: Find Your Balance in Life, tells SELF. "We all perceive experience in a different way even though it is the same experience," he explains. For example, while one person may find the sound of someone typing comforting (if, say, they had a parent who worked on a computer at home), others may associate the sound with office work and become more stressed when they hear it.
Of course, Kelly — who was named one of Teen Vogue's "21 under 21" in November 2018 — is not the only star in the ASMR internet community. The current largest ASMR artist, or "ASMRtist", on YouTube, Taylor Darling, aka ASMR Darling, has two million subscribers and earns an estimated $1,000 a day in advertising revenue. Global megabrands such as IKEA, Sony, McDonald's and Toyota have now all created ASMR-inspired adverts, and in October 2018, platinum rapper Cardi B made an ASMR video that went on to be viewed nearly 10,000,000 times. It's no longer surprising that 75 per cent of children want to be YouTubers, but these kids don't want to be the next beauty-blogging Zoella or game-streaming PewDiePie. They want to be the next brain-tingling ASMR Darling.
"One of our main aims is to try to draw attention to ASMR as a topic worthy (and capable) of scientific research, in the hope that it might galvanise future research efforts," they explain. Of the group, three of them (Emma, Giulia and Tom) experience ASMR, whereas Theresa doesn't. The study is still in an early stage – data collection has just finished – but this diversity in experience, they believe, is a critical component to their research. "So we starting thinking about how we might first and foremost investigate this phenomenon at the most basic level: what might it take to convince someone who doesn't experience ASMR that it is a genuine and consistent experience for some people?" they explain. "Theresa doesn't experience ASMR, and has valuable scepticism of the experience. It adds to the diversity of our research group and the questioning of our approach from a non-ASMR perspective," they add.
Cannot understand this phenomenon making someone "Feel good". The only information here is frustrating to say the least. All speculation and zero facts. I have had this ever since I can remember and it has been nothing but torment. The only thing I have learned is that more people get this than me, people experience it on different levels and with different noises. Other than that this is just people talking about nothing. People say they learned something here. Like what? What's the cause? Can you treat it? Absolute speculation and it was frustrating to read and only walk away with "oh, other people go through this as Well". Name it whatever you want and throw letters behind it, but the fact is you guys know nothing. Congratulations to those who experience this on a pleasurable level, (honestly, that's great) but many of us are tortured by this. If anyone can provide facts and/or science to explain this, PLEASE let me know. It's horrifying and I just want it to go away. It interferes with my love life and all around quality of life and I just want it to stop :/. I don't mean to be rude, it's just a horrible experience and was very disappointed with all the spiritual nonsense and speculation. Just a waste of time so far. Someone Help please
The ASMR videos are easy to laugh at if you're a casual observer–when I recently played one on my iPhone for guests at a dinner party, everyone cracked up within five seconds of watching the video. The videos usually include an attractive woman in a role-play scenario: She's pretending to be an eye doctor, a makeup artist, or even checking hair for head lice. All videos are shot in first person, so the viewer appears to be alone in the room with the woman. And she's usually whispering or speaking softly to you. It's this combination of voice and the sounds from object interaction that the viewer hopes will trigger an ASMR experience.
Satisfying Slime ASMR: With close to 1.5 million subscribers, this is the go-to channel for crunchy slime videos. They post multiple videos a day, all related to slime, games, and toys. Their videos fit into several series related to food slimes, DIY (do it yourself) slimes, cutting stress balls open, and ASMR-specific slimes. Their most popular video about rainbow slime has over 45 million views!
Wow similar and different from me. I listened to ASMR every night for about 6 months when I felt tingles for the first time. It was for probably less than 2 seconds, then a month or two passes before it happens again. But it is happening more often but still randomly. Some weeks I do not get the feeling, other times it is multiple times a week. But every time it is for less than 3 seconds. I am questioning if it is just pins and needles but feels nice because the asmr is so soothing. But you are the first person I have found who had a "delayed" experience. My brain might just be making this up due to my repeated listening and intense research into the subject.
One part of that forage into "Deep Baby Brain" involves introducing you to 'YouTuber' CuteKid4950, and his tub of Strange Creatures goo. He starts off with the usual setup, doing his piece to camera before getting out the gunk. But then… things get weird. "Expanding upon the YouTube infotainment vlog format," Drenge said, "CuteKid4950 takes us from kitchen to basement to warehouse to cave and emerges unscathed and enlightened. We can see the time and space properties of the real world crumble into insignificance. Unusual patterns emerge. Colours and shapes of forgotten solar systems reveal themselves amid the paint and the goo. This is more than something to keep you lightly amused. People will tell you that you are mad. They will try to denounce you. Ignore them. Let history be the judge."
Yes. Mostly cognitive for me as well. I've experienced it hundreds of times while watching movies during particularly tender, deeply emotional, or intellectually stimulating scenes when the actors/narrators speak thoughts that resonate with me. I have also experienced this at church when someone reads scripture or teaches on a subject that suddenly triggers an "aha moment" for me; a feeling of revelation and connection to what I perceive is the spirit of God. Your comment was made a year ago, but I hope you read my response.
ASMR is usually precipitated by stimuli referred to as 'triggers'.[11] ASMR triggers, which are most commonly auditory and visual, may be encountered through the interpersonal interactions of daily life. Additionally, ASMR is often triggered by exposure to specific audio and video. Such media may be specially made with the specific purpose of triggering ASMR or originally created for other purposes and later discovered to be effective as a trigger of the experience.[4]


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Virus-Cell Interactions
Apoptosis of Bystander T Cells Induced by Human Immunodeficiency Virus Type 1 with Increased Envelope/Receptor Affinity and Coreceptor Binding Site Exposure
Geoffrey H. Holm, Chengsheng Zhang, Paul R. Gorry, Keith Peden, Dominique Schols, Erik De Clercq, Dana Gabuzda
Geoffrey H. Holm
1Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115
2Department of Pathology
Chengsheng Zhang
Paul R. Gorry
Keith Peden
3Laboratory of Retrovirus Research, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892
Dominique Schols
4Laboratory of Experimental Chemotherapy, Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium
Erik De Clercq
Dana Gabuzda
For correspondence: dana_gabuzda@dfci.harvard.edu
DOI: 10.1128/JVI.78.9.4541-4551.2004
Apoptosis of uninfected bystander CD4+ T cells contributes to T-cell depletion during human immunodeficiency virus type 1 (HIV-1) pathogenesis. The viral and host mechanisms that lead to bystander apoptosis are not well understood. To investigate properties of the viral envelope glycoproteins (Env proteins) that influence the ability of HIV-1 to induce bystander apoptosis, we used molecularly cloned viruses that differ only in specific amino acids in Env. The ability of these strains to induce bystander apoptosis was tested in herpesvirus saimiri-immortalized primary CD4+ T cells (CD4/HVS), which resemble activated primary T cells. Changes in Env that increase affinity for CD4 or CCR5 or increase coreceptor binding site exposure enhanced the capacity of HIV-1 to induce bystander apoptosis following viral infection or exposure to nonreplicating virions. Apoptosis induced by HIV-1 virions was inhibited by CD4, CXCR4, and CCR5 antibodies or by the CXCR4 inhibitor AMD3100, but not the fusion inhibitor T20. HIV-1 virions with mutant Envs that bind CXCR4 but are defective for CD4 binding or membrane fusion induced apoptosis, whereas CXCR4 binding-defective mutants did not. These results demonstrate that HIV-1 virions induce apoptosis through a CXCR4- or CCR5-dependent pathway that does not require Env/CD4 signaling or membrane fusion and suggest that HIV-1 variants with increased envelope/receptor affinity or coreceptor binding site exposure may promote T-cell depletion in vivo by accelerating bystander cell death.
Human immunodeficiency virus type 1 (HIV-1) infection causes functional impairment and progressive loss of CD4+ T cells, leading to immunodeficiency and AIDS (19, 61). The mechanisms of CD4+-T-cell depletion are poorly understood. Direct lysis of infected CD4+ T cells and apoptosis of bystander cells occur during HIV-1 replication in vitro (15, 36, 39, 41, 44). The relative importance of direct cytopathic effects compared to apoptosis of uninfected bystander cells remains a subject of controversy (36, 39, 41, 44, 52, 53). Most of the apoptotic CD4+ T cells in the peripheral blood and lymph nodes of HIV-1-infected patients are uninfected (4, 17, 30, 45, 62, 64). Increased apoptosis of other types of uninfected cells (i.e., CD8+ T cells, B cells, thymocytes, and neurons) is also detected in AIDS patients (42, 71, 73, 75). These findings suggest that apoptosis of uninfected bystander cells plays an important role in AIDS pathogenesis.
HIV-1 infection can induce cell death in infected and uninfected CD4+ T cells by several different mechanisms. Several HIV-1 proteins, including Tat, Vpr, and Nef, have cytotoxic effects in tissue culture (33, 58, 74, 80). However, the major direct cytopathic effects of HIV-1 are mediated by the viral envelope glycoproteins gp120 and gp41 (Env) (15, 55, 59). The HIV-1 Env can cause direct lysis of infected cells via a mechanism that is dependent on membrane fusion (15, 52, 53). Syncytia formed by the fusion of infected cells also undergo lysis or apoptosis (55). In addition to causing direct cytopathic effects, the HIV-1 Env has been implicated in bystander cell death (28, 42, 44, 65, 78). Soluble, virion-associated, or cell-associated gp120 can prime uninfected T cells for activation-induced or Fas/FasL-mediated apoptosis (5, 21, 29, 42, 80). Alternatively, the HIV-1 envelope glycoproteins can induce proapoptotic signaling via interactions with their receptors (1, 9, 18, 28, 42, 78).
The HIV-1 envelope glycoproteins bind to CD4 and the CCR5 or CXCR4 coreceptors to mediate membrane fusion and virus entry (7, 25). CD4 binding induces exposure of the coreceptor binding site in gp120, which enables binding to a coreceptor. CCR5-tropic isolates (R5 strains) predominate in the early stages of infection, whereas isolates that use both CCR5 and CXCR4 (R5X4 strains) or CXCR4 alone (X4 strains) emerge during the later stages. The emergence of R5X4 or X4 strains frequently correlates with high levels of CD4+-T-cell depletion (20, 46), suggesting that R5X4 and X4 viruses may be more cytopathic than R5 viruses. The higher levels of T-cell depletion induced by R5X4 and X4 viruses compared to R5 viruses is at least partly due to the higher percentage of CD4+ T cells expressing CXCR4 (90 to 100%) compared to CCR5 (15 to 30%) (11, 40), since R5 viruses or soluble R5 gp120 can be highly cytopathic for CCR5-expressing cells (39, 51, 78, 82).
The interactions between the HIV-1 envelope glycoproteins and CD4, CXCR4, and/or CCR5 play an important role in direct and indirect viral cytopathicity (1, 5, 8, 9, 15, 36, 37, 42, 44, 49, 53, 78). These interactions are influenced by properties of the Env that include coreceptor tropism, fusogenicity, and envelope/receptor affinity and by host cell molecules incorporated into the viral envelope (7, 14, 25, 31). HIV-1 isolates differ in their capacities to induce cell death in uninfected and infected cells (36, 38, 44, 49, 51, 65). Determinants of HIV-1 cytopathicity are located in the env gene (15, 37, 44, 53, 65, 78), but properties of the Env that influence bystander cell death have not been defined.
In this study, we investigated properties of the HIV-1 envelope glycoproteins that influence the ability of HIV-1 to induce bystander apoptosis in CD4+ T cells and define the requirements for receptor binding and membrane fusion in the generation of a proapoptotic signal. We demonstrate that HIV-1 variants with increased envelope/receptor affinity or increased exposure of the coreceptor binding site have an enhanced capacity to induce apoptosis in uninfected CD4+ T cells. The induction of bystander apoptosis requires coreceptor binding but not CD4 binding or membrane fusion. These results suggest that HIV-1 virions induce a proapoptotic signal through a CXCR4- or CCR5-dependent pathway that does not require Env/CD4 signaling, membrane fusion, or virus entry and suggest that HIV-1 variants with increased envelope/receptor affinity or coreceptor binding site exposure may promote T-cell depletion in vivo by accelerating bystander cell death.
Cells.293T cells were maintained in Dulbecco's modified Eagle medium supplemented with 10% (vol/vol) bovine calf serum (Sigma Chemical, St. Louis, Mo.) and 100 μg of penicillin and streptomycin/ml. Peripheral blood mononuclear cells (PBMC) were purified from the blood of healthy HIV-1-negative donors by Ficoll-Hypaque density gradient centrifugation and cultured in lymphocyte culture medium (1:1 volume of RPMI 1640 and AIM-V medium [Sigma] supplemented with 10% [vol/vol] fetal bovine serum and 100 μg of penicillin and streptomycin/ml). PBMC were stimulated with 2 μg of phytohemagglutinin (Sigma)/ml for 3 days. The T-cell fraction was isolated by negative selection using a pan-T-cell isolation kit (Miltenyi Biotech, Auburn, Calif.) and cultured in the presence of 10 U of interleukin-2 (Roche Molecular Biochemicals, Indianapolis, Ind.)/ml.
HVS transformation of CD4+ and CD8+ T cells.The herpesvirus saimiri (HVS) subgroup C strain 488 (HVS-C488) was kindly provided by R. Desrosiers. For HVS transformation, primary CD4+ or CD8+ T cells were positively selected using CD4 or CD8 magnetic beads (Miltenyi Biotech) and infected with HVS-C488 as described previously (10). Briefly, 2 × 106 cells were infected with 0.5 ml of HVS-C488 viral stock and incubated at 37°C for 2 h. The cells were then transferred to a T-25 flask and cultured in lymphocyte culture medium supplemented with 10 U of interleukin-2/ml.
Viruses.Plasmids encoding the HIV-1 ELI1, ELI6, and SG3 proviruses have been described previously (32, 34, 67, 81). Plasmids encoding the green fluorescent protein (GFP)-expressing proviruses 89.6-GFP and NL4-3-GFP were generously provided by G. Herbein (60) and C. Aiken, respectively. NL4-3-GFP expresses GFP in place of the nef gene. 89.6-GFP expresses both GFP and a reconstituted nef gene under the control of an internal ribosomal entry site in the nef position. 293T cells were transfected by the calcium phosphate method with 20 μg of provirus plasmid DNA. The medium was replaced after 16 h, and supernatants were harvested after 72 h. Reverse transcriptase (RT) activity in the supernatants was measured using [3H]dTTP incorporation as described previously (70). To generate virus stocks for apoptosis assays, virus produced in 293T cells was used to infect HVS-immortalized CD4+ T cells (CD4/HVS) and infection was monitored by RT assays. After clarification by low-speed centrifugation (200 × g for 5 min), the virus stock supernatants were stored at −80°C. Plasmids containing the HxB, 8x, HxB(V3BaL), and 8x(V3BaL) envelopes (43) and the Hx-IIIB, 8x-IIIB, and 8xD368R-IIIB viruses were generously provided by J. Hoxie. To construct proviruses, the KpnI-BamHI fragment of the envelope plasmids was cloned into pNL4-3, which encodes the NL4-3 provirus, to generate HxB-NL4-3, 8x-NL4-3, HxB(V3BaL)-NL4-3, and 8x(V3BaL)-NL4-3. 293T cells were transfected with 20 μg of provirus plasmid DNA. The medium was replaced after 16 h, and transfected cells were cocultured with SupT1 cells for 12 h. SupT1 cells were then monitored for virus production by RT assay, and virus stock supernatants were harvested as described above. Plasmids expressing the Hx, Hx F522Y, Hx R308A, and Hx R315A envelopes were generously provided by J. Sodroski (6, 53). To generate virus stocks, 293T cells were transfected with 16 μg of the pSVCATΔBgl provirus plasmid (65), 3 μg of envelope plasmid, 4 μg of plasmid expressing HLA-DRα, and 4 μg of plasmid expressing HLA-DRβ7. The medium was replaced after 16 h, and supernatants were harvested after 72 h.
Infections.A total of 3 × 106 cells were incubated with 5 × 104 RT cpm of virus stock for 3 h in 1 ml at 37°C. The cells were washed once and plated in a 6-well tissue culture plate in 3 ml of medium. Twice weekly, the cells were split to keep the total cell density at 106 cells/ml. At these time points, culture supernatant was removed for RT assays and cells were removed for flow cytometric staining.
Flow cytometry.Briefly, 106 cells were washed twice in phosphate-buffered saline (PBS) and stained with 7-aminoactinomycin D (7AAD; Via-Probe; PharMingen) for 15 min at room temperature. For intracellular p24 staining, cells were washed twice in PBS and fixed and permeabilized using a Cytofix/Cytoperm kit (Pharmingen). The cells were resuspended in 50 μl of Perm/Wash buffer and incubated with a 1:200 dilution of the KC57-RD1 α-p24 monoclonal antibody or mouse IgG1-RD1 isotype control (Coulter, Fullerton, Calif.) for 20 min at 4°C. For staining of apoptotic cells, the cells were washed twice with Perm/Wash buffer and then stained using a terminal dUTP nick-end labeling (TUNEL) kit (In Situ Cell Death Detection kit; Roche) as directed by the manufacturer. The cells were then washed twice with PBS and analyzed using a FACScan flow cytometer (Becton Dickinson, San Jose, Calif.) or an Epics XL flow cytometer (Coulter). Data were analyzed using Cell Quest (Becton Dickinson) and Expo32 (Coulter) software.
CD4 affinity.A total of 3 × 106 CD4/HVS T cells were infected with 105 RT cpm of ELI1 and ELI6 as described above. Five days postinfection, 2 × 106 cells were washed twice with PBS containing 2% bovine serum albumin and 0.02% sodium azide. Then, 106 cells were incubated with increasing concentrations of soluble CD4-immunoglobulin (Ig) (6) for 45 min at 37°C, while the remaining 106 cells were incubated with 10 μg of a human anti-gp120 antibody (ImmunoDiagnostics [Woburn, Mass.] no. 2501)/ml for 45 min at 4°C. Both sets of cells were then washed twice and incubated with a goat anti-human Ig-phycoerythrin (PE) antibody (Jackson ImmunoResearch, West Grove, Pa.) for 45 min at 4°C. The cells were washed twice and analyzed using an Epics XL flow cytometer. Data were analyzed using Expo32 (Coulter) and Prism (GraphPad, San Diego, Calif.) software.
Apoptosis induced by nonreplicating virions.To determine the ability of HIV-1 to induce apoptosis in the absence of virus replication, 106 CD4+ HVS T cells were preincubated in lymphocyte medium with 1 μΜ 3′-azido-3′-deoxythymidine (AZT; Sigma) for 1 h at 37°C prior to incubation with virus stocks produced in CD4/HVS T cells or SupT1 cells, unless otherwise indicated. Alternatively, virions were UV inactivated for 45 min. Some samples were also preincubated for 1 h with 10 μg of anti-CD4 antibody (QS4120 [Calbiochem, San Diego, Calif.] and RPA-T4 [Pharmingen])/ml, 10 μg of anti-CXCR4 antibody (12G5; PharMingen)/ml, 10 μg of anti-CCR5 antibody (2D7; Pharmingen)/ml, 5 μg of anti-gp120 antibody (1b12; kindly provided by J. Sodroski and D. Burton)/ml; cross-reactive anti-gp120 (ImmunoDiagnostics no. 1121), 1.2 μM AMD3100 (26, 72), or 1 μg of T20 (American Peptide Co., Sunnyvale, Calif.)/ml. One hundred thousand RT units of virus, or an equivalent volume of supernatant from uninfected control CD4+ HVS T cell or SupT1 cultures, were added to the cells. As an additional control, some samples were incubated with virus stock supernatant that had been cleared of pelletable components, including virions, by centrifugation at 15,000 × g for 1 h. The cells were incubated for 72 h, stained with 7AAD, α-p24-RD1, and TUNEL-fluorescein isothiocyanate (FITC) as described above and analyzed by flow cytometry.
HIV-1 infection induces bystander apoptosis in CD4/HVS cells.To investigate the ability of HIV-1 to induce apoptosis in uninfected bystander T cells, we used HVS-immortalized CD4+- and CD8+-T-cell lines derived from the peripheral blood T lymphocytes of an HIV-negative healthy donor. These cell lines resemble activated mature human CD4+ and CD8+ T lymphocytes (10), as indicated by high expression of activation markers such as CD25, HLA-DR, and CD95/Fas (Table 1). These cell lines express high levels of CXCR4 and CCR5 (Table 1) and were derived from one donor, eliminating confounding effects of donor variability. Furthermore, HVS-immortalized T cells have been shown to be susceptible to apoptosis (48).
Characterization of immortalized CD4+ and CD8+ T cells
CD4/HVS cells were infected with the highly fusogenic X4 HIV-1 isolate SG3 (34), which has been shown to induce high levels of bystander apoptosis in primary brain cultures (65). SG3 replicated to high levels, peaking on days 7 to 11 (data not shown). On days 7 (Fig. 1) and 14 (data not shown), cells were stained with 7AAD, anti-p24-PE, and TUNEL-FITC and analyzed by flow cytometry. 7AAD was used to exclude necrotic cells, including cells killed by single-cell lysis, and debris from the p24/TUNEL analysis. On day 7, approximately 8% of cells in SG3-infected cultures were 7AAD positive, compared to 3% of the cells in control cultures. Approximately 1.5% of the cells were 7AAD-p24 double positive, representing cells undergoing single-cell lysis. SG3 infection induced high levels of apoptosis (26 to 31%), which were up to 25-fold higher than those observed in uninfected control cultures. Approximately 18 to 27% of the cells in cultures infected with SG3 stained positive for p24. However, only 2 to 6% were TUNEL-p24 double positive. Thus, up to 80% of the apoptotic cells were not productively infected.
Flow cytometric analysis of apoptosis in CD4/HVS T cells infected with SG3. Cells were infected with SG3 as described in Materials and Methods and stained on day 7 with TUNEL-FITC, anti-p24-PE, and 7AAD and analyzed by flow cytometry. 7AAD-positive cells were gated out of the TUNEL/p24 analysis.
The ELI6 variant induces higher levels of bystander apoptosis in CD4/HVS T cells than the parental primary X4 isolate ELI1.To determine whether changes in the viral Env that increase affinity for CD4 also enhance the capacity of HIV-1 to induce bystander apoptosis, we used the primary X4 HIV-1 isolate ELI1 and the variant ELI6, which was derived by adapting ELI1 to growth in T-cell lines. The resulting envelope mutations in the adapted virus were cloned back into ELI1 to create ELI6, which is isogenic to ELI1 except for the point mutations G427R, in the C4 domain of gp120 near the CD4 binding site, and M7V, in the fusion domain of gp41 (32, 67, 81). Previous studies have shown that ELI6 has an increased ability to bind to CD4, enhanced fusogenicity on cells expressing low levels of CD4, and increased susceptibility to sCD4-induced gp120 shedding compared to ELI1 (32, 47, 67, 81), suggesting an increase in viral affinity for CD4.
To investigate the ability of ELI1 and ELI6 to induce apoptosis during infection of CD4+ T cells, CD4/HVS cells were infected with these viruses. Cells infected with SG3 were used as a positive control. All of the viruses replicated to high levels and exhibited similar replication kinetics, with replication peaking on day 7 (data not shown). On days 7 and 11, cells were stained with 7AAD, anti-p24-PE, and TUNEL-FITC and analyzed by flow cytometry. Approximately 21 to 24% of cells in infected cultures were p24 positive on day 7, and 12 to 20% were p24 positive on day 11 (Fig. 2). The amount of p24 staining varied among cultures infected with different viruses and did not always correlate directly with RT levels. This discrepancy might reflect the measurement of RT values at discrete time points, which may not accurately reflect daily variations in replication kinetics. On days 7 and 11, high levels of apoptosis above background (29 to 54%) were seen in infected cultures (Fig. 2) and less than 10% of the cells were TUNEL-p24 double positive. Up to 47% of the cells were TUNEL positive and p24 negative, representing bystander cells that were not productively infected. On days 7 and 11, ELI6 induced apoptosis in a greater total number of cells and in more p24-negative cells than ELI1. Levels of cells that were TUNEL-7AAD double positive were similar among the infected cell cultures (not shown). Thus, an adapted variant with increased ability to bind to CD4 and increased fusogenicity had a greater capacity to induce bystander apoptosis than the parental virus.
Flow cytometric analysis of apoptosis in CD4/HVS T cells infected with X4 HIV-1 viruses. Cells were infected with equivalent amounts of SG3, ELI1, or ELI6 as described in Materials and Methods and cultured for 2 weeks. On days 7 and 11, cells were stained with TUNEL-FITC and anti-p24-PE and analyzed by flow cytometry. 7AAD-positive cells were gated out of the TUNEL/p24 analysis. Results are representative of six independent experiments.
In the preceding experiment, we could not exclude the possibility that some TUNEL-positive, p24-negative cells may have been recently infected and therefore may not produce detectable levels of p24. To verify that HIV-1 infection induces apoptosis in uninfected bystander CD4/HVS T cells, we performed additional experiments using recombinant viruses that contain a gene for GFP either in place of the nef gene (NL4-3-GFP) or under the control of an internal ribosomal entry site in tandem with nef gene expression (89.6-GFP) (41). Because GFP is expressed as an early viral gene product, GFP expression is a sensitive marker for infected cells (41). CD4/HVS cells were infected with the R5X4 89.6-GFP virus or X4 NL4-3-GFP virus and stained on days 7, 10, and 14 with 7AAD and annexin-V-PE. GFP expression was used to detect infected cells, and annexin-V was used to detect apoptotic cells. 7AAD-positive cells were excluded from the GFP and annexin-V analysis. The infection peaked on day 10, with approximately 5% of the cells in the 89.6-infected culture and 8% of the cells in the NL4-3-infected culture being positive for GFP expression (Fig. 3). Annexin-V staining increased over time in the infected cultures, from approximately 5% on day 7 to approximately 12% on day 10 and 30 to 45% on day 14. At all time points, the fraction of GFP-annexin-V double-positive cells was only a small percentage (5 to 8%) of the total annexin-V-positive fraction, suggesting that the majority of apoptotic cells were uninfected (Fig. 3). Staining with anti-p24-PE showed that all of the GFP-positive cells were p24 positive (data not shown), indicating that staining with the anti-p24 antibody labeled all of the productively infected cells. Furthermore, over 97% of syncytia in CEMx174 T-cell cultures infected with serial dilutions of the GFP-expressing viruses were GFP positive (data not shown), indicating that the viruses were capable of expressing GFP in all productively infected cells and did not delete the exogenous gene. Collectively, these results indicate that HIV-1 infection induces apoptosis in uninfected CD4/HVS T cells.
Flow cytometric analysis of apoptosis in CD4/HVS T cells infected with GFP-expressing HIV-1 viruses. Cells were infected with equivalent amounts of 89.6-GFP and NL4-3-GFP as described in Materials and Methods and stained with annexin-V-PE and 7AAD on days 7, 10, and 14. 7AAD-positive cells were gated out of the analysis of annexin-V-positive cells (white columns), GFP-positive cells (gray columns), or annexin-V-GFP double-positive cells (black columns). Results are representative of two independent experiments.
ELI6 has increased affinity for CD4 compared to ELI1.To verify that ELI6 has a higher affinity for CD4 compared to ELI1, we measured the binding of a range of concentrations of sCD4-IgG to Env expressed on the surface of CD4/HVS T cells infected with these viruses. Five days postinfection, cells were incubated with increasing concentrations of sCD4-IgG, stained with a PE-conjugated anti-human IgG antibody, and analyzed by flow cytometry. Matched cells were incubated with a human anti-gp120 antibody and stained with PE anti-human IgG, and the sCD4-IgG binding data were normalized for relative gp120 expression on the cell surface and for background sCD4-IgG binding to uninfected control cells. Nonlinear regression analysis was used to generate a binding curve and calculate the CD4 dissociation constants for the two viruses (Fig. 4). These studies demonstrated that ELI6 has an increased affinity for sCD4-IgG compared to ELI1, with dissociation constants of 21 versus 127 nM, respectively.
ELI6 has a higher affinity for CD4 than does ELI1. CD4/HVS T cells were infected with ELI1 or ELI6. Five days postinfection, cells were incubated with sCD4-IgG and stained with an anti-human IgG-PE antibody as described in Materials and Methods. Matched cells were incubated with a human anti-gp120 antibody and stained with an anti-human IgG-PE antibody. Cells were analyzed by flow cytometry, and the sCD4-IgG binding data were normalized for relative gp120 expression on the cell surface and for background sCD4-IgG binding to uninfected control cells. MFI, mean fluorescence intensity. The quantitation represents means and standard deviations (error bars) of duplicate samples. Results are representative of two independent experiments.
Nonreplicating HIV-1 virions induce apoptosis in CD4/HVS cells.The preceding experiments demonstrated distinct differences in the levels of bystander apoptosis induced by viruses that differ in their affinities for CD4. However, we could not control for effects that might be caused by differences in replication kinetics. Therefore, we developed assays to examine T-cell apoptosis in the absence of viral replication. CD4/HVS cells were preincubated with 1 μM AZT to inhibit reverse transcription and prevent productive virus replication and were then incubated with HIV-1 virions. Alternatively, virions were UV inactivated for 45 min prior to incubation with CD4/HVS cells. Cultures were monitored for p24-positive cells for 7 days to confirm the absence of virus replication. No p24-positive cells were detected (data not shown), indicating that virus replication did not occur. Following 72 h of incubation with SG3, ELI1, or ELI6, TUNEL staining was performed to detect apoptotic cells. HIV-1 virions induced apoptosis in approximately two- to fourfold more cells than did control supernatants (11 to 20% versus 5%) (Fig. 5A). ELI6 induced apoptosis in twofold more cells than did ELI1 (20 versus 11%). In contrast to the results observed in CD4/HVS cells, none of the viruses induced apoptosis in CD8/HVS cells (Fig. 5B). These results suggest that increased viral affinity for CD4 and/or increased fusogenicity can enhance the ability of HIV-1 virions to induce bystander apoptosis in CD4+ T cells.
HIV-1 virions induce apoptosis in CD4+ T cells in the absence of virus replication. CD4/HVS T cells (A and C) and CD8/HVS T cells (B) were preincubated with 1 μM AZT and then incubated with control supernatants or HIV-1 virions or with the nonpelletable fraction (S15) of control or viral stock supernatants (C) as described in Materials and Methods. After 72 h, cells were stained with TUNEL-FITC (black columns) and 7AAD (data not shown). 7AAD-positive cells were gated out of the TUNEL analysis. The quantitation represents means and standard deviations (error bars) of triplicate samples. *, P < 0.05; **, P < 0.005 versus control by Student's two-tailed t test. Results are representative of six independent experiments.
The virus stocks used in the preceding experiments were produced in CD4/HVS cells, raising the possibility that soluble factors in the virus stock, such as inflammatory cytokines or soluble gp120, may have contributed to the induction of apoptosis. In particular, ELI6 was shown to be highly susceptible to soluble CD4-induced gp120 shedding (47, 81), raising the possibility that soluble gp120 could have contributed to the induction of bystander apoptosis. To address these questions, virions were removed from the virus stock by centrifugation and CD4/HVS cells were incubated with the nonpelletable (S15) fraction for 72 h. In contrast to ELI6 virus stock, the S15 fraction did not induce apoptosis in CD4/HVS T cells (Fig. 5C). These results indicate that CD4/HVS T-cell apoptosis is induced primarily by HIV-1 virions rather than by soluble gp120 or other soluble factors present in the virus stocks.
Apoptosis induced by nonreplicating HIV-1 virions is inhibited by anti-CD4, -CXCR4, and -gp120 monoclonal antibodies and by the CXCR4 inhibitor AMD3100, but not by the fusion inhibitor T20.To determine whether CD4/HVS T-cell apoptosis induced by HIV-1 virions can be inhibited by blocking the interaction between gp120 and its receptors or preventing virus-cell fusion, we used monoclonal antibodies against CD4, CXCR4, or gp120, the CXCR4 inhibitor AMD3100, and T20, an HIV-1 fusion inhibitor (56). The CD4 antibodies QS4120 and RPA-T4 bind to domain 1 of CD4 and prevent binding to gp120. The CXCR4 antibody 12G5 binds to the first and second extracellular loops of CXCR4 and blocks infection by X4 HIV-1 strains. The gp120 antibodies 1b12 and ImmunoDiagnostics no. 1121 neutralize HIV-1 infection and syncytium formation. CD4/HVS cells were incubated for 1 h with 1 μM AZT and an antibody or inhibitor and then with ELI6 virions for 72 h. Apoptosis induced by HIV-1 virions was significantly reduced by preincubation with CD4, CXCR4, or gp120 antibodies (Fig. 6A) or AMD3100 (Fig. 6B) (P < 0.05). QS4120 and RPA-T4 inhibited apoptosis induced by ELI6 by 40 to 50%, whereas 12G5 and the gp120 antibodies inhibited apoptosis by 60 to 65%. AMD3100 had the most potent inhibitory effect, inhibiting apoptosis by approximately 80%. In contrast, concentrations of the fusion inhibitor T20 that completely blocked virus infection (data not shown) did not inhibit apoptosis induced by ELI6. Thus, virions induce a proapoptotic signal through a CD4- or CXCR4-dependent pathway that does not require membrane fusion or virus entry.
Inhibition of apoptosis by CD4, CXCR4, and gp120 antibodies and AMD3100. CD4/HVS T cells (A and B) or primary T cells (C) were preincubated for 1 h with 1 μM AZT and antibodies against CD4 (QS4120 and RPA-T4), CXCR4 (12G5), or gp120 (1B12 or Immunodx [ImmunoDiagnostics no. 1121]), the CXCR4 antagonist AMD3100, or the fusion inhibitor T20 as indicated and then incubated with ELI6 virions as described for Fig. 5. After 72 h, cells were stained with TUNEL-FITC (black columns) and 7AAD (data not shown). 7AAD-positive cells were gated out of the TUNEL analysis. The quantitation represents means and standard deviations (error bars) of triplicate samples. *, P < 0.05 versus ELI6 alone; **, P < 0.05 versus control by Student's two-tailed t test. Results are representative of two independent experiments.
We then examined the ability of ELI6 virions to induce apoptosis in primary T cells. Primary CD4+ and CD8+ T cells were negatively selected from phytohemagglutinin-stimulated PBMC and incubated with 105 RT counts of UV-inactivated ELI6 for 72 h. Cultures were then stained to detect apoptotic cells. ELI6 virions induced twofold higher levels of apoptosis over background (Fig. 6C). The absence of viral replication was confirmed by p24 staining and by RT assay of the culture supernatant. The monoclonal antibody 12G5 and CXCR4-inhibitor AMD3100 inhibited apoptosis induced by ELI6 by up to 77% (P < 0.05). Thus, binding of the Env to CXCR4 is required for apoptosis induced by nonreplicating X4 HIV-1 virions in primary T cells.
Apoptosis induced by nonreplicating HIV-1 virions requires CXCR4 binding but not CD4 binding or membrane fusion.Previous studies have suggested that X4 HIV-1 virions induce a proapoptotic signal through CD4 and/or CXCR4 (13, 44, 69). However, whether CD4 binding and membrane fusion are required for the generation of the proapoptotic signal are unclear. To address this issue, we used mutant Envs that are defective for binding to CD4 or CXCR4 or for fusion with target cells. Virions were pseudotyped with the wild-type HxBc2 Env (Hx), an Hx Env with a mutation in the fusion peptide, F522Y, which abolishes the ability of the Env to fuse (53), or an Hx Env with a mutation in the V3 loop, either R308A or R315A, which abolishes CXCR4 binding (6).
During initial experiments, we found that pseudotyped virions produced by transient transfection of 293T cells did not induce apoptosis in CD4/HVS T cells (data not shown). One possible explanation for this unexpected result is that 293T cells do not express certain proteins such as major histocompatibility complex (MHC) class II and ICAM-1, which are expressed on T cells, become incorporated into the HIV-1 envelope, and enhance the ability of virions to induce apoptosis (2, 12, 14, 27, 28). Consistent with the results of previous studies (27, 28), we found that virions produced from 293T cells cotransfected with MHC class II isoforms HLA-DRα/β1 or HLA-DRα/β7 had the capacity to induce apoptosis in CD4/HVS T cells at levels similar to those induced by virions produced in T cells (data not shown). Therefore, virions for subsequent experiments were produced in 293T cells by cotransfecting an env− provirus plasmid with a plasmid expressing an HIV-1 envelope and plasmids expressing MHC class II DRα/β7.
UV-inactivated virions pseudotyped with wild-type or mutant Hx Envs were incubated with CD4/HVS T cells for 72 h. Virions pseudotyped with the wild-type Hx Env induced significantly higher levels of apoptosis compared to control supernatants (P < 0.05) (Fig. 7A). Virions pseudotyped with a fusion-defective Env containing the F522Y mutation induced similar levels of apoptosis compared to virions pseudotyped with the Hx Env, as did virions in cultures incubated with T20 (Fig. 7A). In contrast, virions pseudotyped with Envs defective for binding to CXCR4 (R308A or R315A) did not induce significant levels of apoptosis (Fig. 7A). These data suggest that CXCR4 binding, but not membrane fusion or virus entry, is required for HIV-1 virions to induce apoptosis in CD4/HVS T cells.
CXCR4 binding, but not CD4 binding or membrane fusion, is required for induction of apoptosis by HIV-1 virions. CD4/HVS T cells were incubated with equivalent amounts of UV-inactivated HIV-1 virions pseudotyped with wild-type or mutant (A and C) Env or were preincubated with 1 μM AZT for 1 h and then incubated with equivalent amounts of ELI6 virions or NL4-3 virions containing the HxB, 8x, HxB(V3BaL), or 8x(V3BaL) envelopes (B). CD4/HVS T cells were preincubated with AMD3100 for 1 h prior to incubation with virions where indicated (C). After 72 h, cells were stained with TUNEL-FITC and 7AAD (data not shown). 7AAD-positive cells were gated out of the analysis. The quantitation represents means and standard deviations (error bars) of triplicate samples. *, P < 0.05 versus control by Student's two-tailed t test. Results are representative of two independent experiments.
To further explore the relationship between CD4 binding, coreceptor binding, and apoptosis, we used viruses with envelope glycoproteins that interact with coreceptors independently of CD4. 8x and 8x(V3BaL) are CD4-independent HIV-1 viruses that can utilize CXCR4 or CCR5, respectively, in the absence of CD4 to mediate fusion and virus entry (43, 54). However, these viruses retain the ability to bind to CD4 and the efficiency of these strains is enhanced when CD4 is present (43). The 8x virus, derived by passage on cells lacking CD4, contains point mutations in the Env that increase exposure of the coreceptor binding site and allow coreceptor binding in the absence of CD4. These conformational changes are also associated with increased fusogenicity (43, 54). The 8x(V3BaL) virus was derived by replacing the V3 loop of 8x with the V3 loop from BaL, conferring R5 tropism to the virus. To determine whether increased exposure of the coreceptor binding site is associated with an increased ability of these variants to induce bystander cell death compared to the parental viruses, we cloned the 8x and 8x(V3BaL) envelopes and their parental envelopes, HxB and HxB(V3BaL), respectively, into the NL4-3 provirus and then tested the ability of these viruses to induce apoptosis in CD4/HVS cells in the absence of virus replication. 8x-NL4-3 and 8x(V3BaL)-NL4-3 virions induced twofold higher levels of apoptosis compared with the HxB-NL4-3 and HxB(V3BaL)-NL4-3 parental controls (P < 0.05) (Fig. 7B). These results suggest that increased exposure of the coreceptor binding site is associated with an enhanced capacity of X4 and R5 HIV-1 virions to induce bystander apoptosis.
The 8x envelope glycoprotein does not require CD4 expression on target cells in order to bind CXCR4 and trigger membrane fusion but retains the ability to bind to CD4 when it is present on the target cell surface. To determine the requirement for CD4 binding in the generation of a proapoptotic signal by HIV-1 virions, we used a mutant of 8x, 8xD368R, that cannot bind to CD4 while retaining the ability to bind CXCR4 directly. Virions pseudotyped with either the 8x or 8xD368R envelope induced significantly higher levels of apoptosis in CD4/HVS T cells than control supernatants (P < 0.05) (Fig. 7C). 8x virions induced slightly higher levels of apoptosis than did 8xD368R, but this difference was not statistically significant, suggesting that CD4 binding is not required for HIV-1 virions to induce apoptosis. Blocking the interaction between Env and CXCR4 with AMD3100 inhibited the induction of apoptosis by 8x and 8xD368R virions (Fig. 7C). Thus, HIV-1 virions induce a proapoptotic signal through CXCR4. In contrast, Env signaling through CD4 is not required for virion-induced apoptosis. SDF-1, the natural ligand of CXCR4, can induce both survival and apoptotic signaling in primary CD4+ T cells (79). At concentration ranges of 1 to 10 μg/ml, we found that SDF-1 treatment for 72 h induced low levels of apoptosis over background in CD4/HVS T cells (data not shown). Thus, CXCR4-mediated signaling induced by the physiological ligand at high concentrations can induce apoptotic signaling in CD4/HVS T cells.
Affinity for CCR5 influences the ability of nonreplicating R5 virions to induce apoptosis.To investigate whether the ability of HIV-1 virions to induce apoptosis is influenced by changes in Env that increase affinity for a coreceptor, we used viruses adapted to growth in the presence of the small-molecule CCR5 inhibitor AD101 (77). These viruses were derived by serial passage of the parental primary R5 virus CC1/85 under the selection of AD101 to generate CC101.6 and CC101.19, selected after 6 and 19 weeks of passage, respectively. CCCon19 is a control virus passaged for 19 weeks without selection. UV-inactivated CC101.19, and to a lesser extent CC101.6, virions induced higher levels of apoptosis in CD4/HVS T cells than the parental virus or the passaged control virus (Fig. 8A). 25-3, which contains the CC101.19 envelope gene cloned into NL4-3, induced significantly higher levels of apoptosis than 9-8, which contains the cloned CC1/85 parental envelope (50) (P < 0.05) (Fig. 8A). Apoptosis induced by 25-3 was inhibited by the CCR5 antibody 2D7, a gp120 antibody, and the small-molecule CCR5 inhibitor TAK-779 and was partially blocked by a CD4 antibody (Fig. 8B and data not shown). These findings suggest that changes in the Env that increase viral affinity for CCR5 can also enhance the capacity of HIV-1 virions to induce bystander apoptosis in CD4/HVS T cells.
Apoptosis induced by HIV-1 virions with increased affinity for CCR5. CD4/HVS T cells were incubated with equivalent amounts of UV-inactivated CC1/85, CC101.6, CC101.19, CCCon19, 9-8, or 25-3 HIV-1 virions (A) or were preincubated with antibodies against CCR5 (2D7), gp120 (1b12), or CD4 (QS4120) or control IgG for 1 h and then incubated with equivalent amounts of 25-3 (B). After 72 h, cells were stained with TUNEL-FITC and 7AAD (data not shown). 7AAD-positive cells were gated out of the analysis. The quantitation represents means and standard deviations (error bars) of triplicate samples. *, P < 0.05 versus control (A and B); **, P < 0.05 versus 25-3 alone (B) by Student's two-tailed t test. Results are representative of two independent experiments.
The immunologic and virologic mechanisms that lead to bystander CD4+-T-cell death during HIV-1 infection remain poorly understood. In this study, we investigated HIV-1-induced bystander apoptosis in HVS-immortalized CD4+ T cells, which resemble activated mature primary CD4+ T cells (10). We found that infection of CD4/HVS T cells with X4 or R5X4 strains caused high levels of bystander apoptosis. Furthermore, exposure of CD4/HVS T cells to HIV-1 virions induced apoptosis in the absence of productive infection. Changes in the Env that increase envelope/receptor affinity or coreceptor binding site exposure enhanced the capacity of HIV-1 virions to induce bystander apoptosis. These results suggest that HIV-1 variants with increased envelope/receptor affinity and/or enhanced coreceptor binding site exposure may promote T-cell depletion in vivo by accelerating bystander CD4+-T-cell death
The relative importance of direct cytopathicity versus bystander apoptosis during HIV-1 infection in vitro and in vivo has been the subject of much debate (15, 16, 28, 37, 40, 42, 44, 52, 53). Direct cytopathic effects are the predominant cause of CD4+-T-cell death in T-cell lines infected with lab-adapted HIV-1 strains (15, 52, 53, 55, 57), whereas apoptosis of both infected and uninfected CD4+ T cells occurs in lymphoid tissue explants infected with lab-adapted or primary strains (37, 44). Several groups have reported that HIV-1-induced bystander apoptosis in primary T cells is highly dependent on the presence of monocytes/macrophages (3, 21, 41, 42, 66), which can prime T cells to undergo apoptosis induced by Fas, tumor necrosis factor alpha, or gp120 (3, 21, 42, 66) and are present in human lymphoid tissue explants (35, 37, 44). Remarkably, we found that high levels of bystander apoptosis are induced by infection of CD4/HVS T cells with primary X4 HIV-1 isolates (SG3 and ELI1), or GFP-expressing X4 and R5X4 recombinant strains (NL4-3-GFP and 89.6-GFP), in the absence of monocytes/macrophages and other antigen-presenting cells. CD4/HVS T cells are highly activated (10) and therefore may not require priming by antigen-presenting cells to undergo bystander apoptosis. Thus, apparent discrepancies in the literature on HIV-1-mediated killing of infected versus uninfected cells may in part reflect differences between experimental systems, such as the level of T-cell activation and the cell culture microenvironment.
The fusion inhibitor T20 prevented virus entry but did not inhibit the induction of apoptosis by HIV-1 virions. Moreover, the levels of apoptosis induced by HIV-1 virions pseudotyped with a fusion-defective mutant Env were similar to those induced by virions with wild-type Env. These results imply that membrane fusion is not required for HIV-1 to induce bystander apoptosis and argue against a "fusion from without" mechanism in which HIV-1 particles induce massive cell membrane fusion leading to membrane permeability and cell death. We used flow cytometric analysis to detect p24 antigen or GFP as a marker for productively infected cells. One concern is whether all of the presumed bystander cells are truly uninfected, since this method may not detect infected cells in the early stages of the replication cycle. A similar concern applies to studies using cultures treated with AZT where viruses enter cells but replication is blocked during reverse transcription. However, our experiments using T20 and a fusion-defective mutant indicate that virus entry and the early steps of infection are not required for HIV-1-induced bystander apoptosis and suggest a critical role for events prior to membrane fusion.
HIV-1 virions with Envs defective for CXCR4 binding were also defective for inducing apoptosis in CD4/HVS T cells. Furthermore, AMD3100 and an anti-CXCR4 monoclonal antibody inhibited apoptosis induced by X4 HIV-1 virions. Likewise, TAK-779 and an anti-CCR5 monoclonal antibody inhibited apoptosis induced by R5 HIV-1 virions. These findings suggest that binding of the Env to CXCR4 or CCR5 is required for the induction of bystander apoptosis. CXCR4- and CCR5-dependent signal transduction pathways include activation of G proteins and the focal adhesion tyrosine kinases Pyk2 and FAK along with the proapoptotic p38 mitogen-activated protein kinase (22, 23, 63, 69). To test whether the proapoptotic signal is Gαi-dependent, we incubated CD4/HVS T cells with pertussis toxin (1 μg/ml) prior to the addition of HIV-1 virions (G.H.H. and D.G., unpublished observation). However, the results could not be interpreted because pertussis toxin treatment caused high background levels of apoptosis. Further studies are required to determine the role of specific signaling pathways in bystander apoptosis induced by HIV-1 virions.
In contrast to the requirement for coreceptor binding, CD4 binding was not intrinsically required for HIV-1-induced bystander apoptosis. In particular, HIV-1 virions with envelope glycoproteins that interact directly with CXCR4 but are defective for CD4 binding retained the ability to induce apoptosis. Furthermore, bystander apoptosis was inhibited by AMD3100 and an anti-CXCR4 monoclonal antibody, which do not interfere with the binding of gp120 to CD4. These results contrast with previous studies, which suggested that the HIV-1 Env induces proapoptotic signals through CD4 (1, 5, 8). However, Env binding to CD4 leads to subsequent Env-coreceptor binding by triggering exposure of the coreceptor binding site (25). Thus, Env binding to CD4 indirectly leads to coreceptor engagement. CD4-mediated signaling can prime T cells for activation-induced apoptosis and/or enhance coreceptor-mediated signaling pathways (5, 21, 66, 76). However, our studies suggest that Env-CD4 binding is not sufficient to induce apoptosis in the absence of Env-coreceptor binding.
Changes in the envelope glycoproteins that increase envelope/receptor affinity or coreceptor binding site exposure enhanced the capacity of HIV-1 to induce bystander apoptosis. These strain-dependent differences were independent of effects on replication efficiency, as they were also observed in experiments using nonreplicating virions. Mechanistically, these properties of the envelope glycoproteins can impact bystander apoptosis by enhancing Env-coreceptor interactions and thereby increasing the intensity of coreceptor-mediated proapoptotic signaling. To this end, increased viral affinity for CD4 could indirectly enhance coreceptor-mediated signaling by increasing virion attachment and coreceptor binding site exposure (25). Alternatively, HIV-1 virions with increased affinity for CD4 may have a greater capacity to induce apoptosis in cells that express CD4 at low levels (25, 38, 47). Bystander apoptosis can also be influenced by certain host cell proteins, such as MHC class II and ICAM-1, which are incorporated into HIV-1 virions (12, 27, 28; G.H.H. and D.G., unpublished results). Consistent with these findings, we found that virions produced in 293T cells did not induce apoptosis in CD4/HVS T cells unless provirus plasmids were cotransfected with MHC class II isoforms. Incorporation of MHC class II molecules into HIV-1 virions may enhance binding to target cells via interactions with CD4 and/or induce signaling events that prime T cells to undergo apoptosis.
In summary, our experiments suggest that HIV-1 virions induce a proapoptotic signal in CD4+ T cells through a CXCR4- or CCR5-mediated pathway that does not require CD4 signaling or membrane fusion. The ability of HIV-1 to induce bystander apoptosis is influenced by properties of the Env that enhance envelope/coreceptor interactions, including envelope/receptor affinity, exposure of the coreceptor binding site, and host cell membrane proteins on the virion surface. Previous studies have estimated that only 0.00001 to 0.01% of HIV-1 virions are infectious in vitro and in vivo (24, 68). Thus, noninfectious virions may contribute to HIV-1 pathogenicity in vivo by inducing bystander apoptosis mediated by Env-coreceptor interactions. Therapeutic strategies to block these interactions may reduce CD4+-cell depletion in AIDS patients.
We thank J. Sodroski, J. LaBonte, J. Hoxie, and J. Wang for helpful discussions. We are also grateful to J. Sodroski for providing the Hx, Hx F522Y, Hx R308A, and Hx R315A envelopes, J. Sodroski and D. Burton for providing the 1b12 antibody, J. Hoxie for providing the HxB, HxB(V3BaL), 8x, 8x(V3BaL), and 8xD368R envelopes, J. Moore and S. Kuhmann for providing the CC1/85, CC101.6, CC101.19, CCCon.19, 25-3, and 9-8 viruses, R. Desrosiers for providing owl monkey kidney cells and HVS-C488, G. Herbein for providing 89.6-GFP, C. Aiken for providing NL4-3-GFP, and ImmunoDiagnostics, Inc., for providing the cross-reactive anti-gp120.
This work was supported by NIH NS35734 to D.G. Core facilities were supported by Center for AIDS Research grants (AI28691) and a DFCI/Harvard Center for Cancer Research grant. D.G. is an Elizabeth Glaser Scientist who was supported by the Pediatric AIDS Foundation.
Received 6 November 2003.
Accepted 22 December 2003.
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Journal of Virology Apr 2004, 78 (9) 4541-4551; DOI: 10.1128/JVI.78.9.4541-4551.2004
You are going to email the following Apoptosis of Bystander T Cells Induced by Human Immunodeficiency Virus Type 1 with Increased Envelope/Receptor Affinity and Coreceptor Binding Site Exposure
Bystander Effect
CD4-Positive T-Lymphocytes

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Super Dimensional Analysis
An academic examination of Robotech, Macross, and other original source materials
Loving the Alien, Hating the Hybrid: A Cultural Study of Robotech by Chris Mich
Below is a brief synopsis and peer review of an article titled "Loving the Alien, Hating the Hybrid: A Cultural Study of Robotech" published in the Academic peer reviewed MOSF (Museum of Science Fiction) Journal of Science Fiction Volume 2, Issue 1, September 2017 ISSN 2472-0837 (International Standard Serial Number). The article was written by Christopher H. Mich. It was published in September of 2017. The author's twitter is @ChrisMich1.
This 9 page article is available for free here, here, here, and here.
Abstract 1. Taken from Mr. Mich's article and reprinted here.
In 1985, young science fiction fans were starving for entertainment to fill the void left with the 1983 conclusion of the original Star Wars trilogy. These fans suffered through poorly produced television series and films that did not capture the emotion, drama and mythos of the Star Wars trilogy. Enter Robotech – the brainchild of Writer/Producer Carl Macek. A fan of Japanese Animation (also known as "anime" or "Japanimation"), Macek acquired the rights to three separate anime television programs. With each series deemed too short to run as individual series on American television, Macek melded all three series into one overall series under the Robotech title. The series focus isn't limited to the universal war unfolding but to how the war affects individual characters' personal relationships. In Macek's own words, Robotech is more "soap opera" than space opera (Macek, VIII, 1985). Yet, a textual analysis of Robotech reveals that the franchise actually promotes the supposed need for racial purity/isolationism and that the hybrid is truly something to be feared. And, as the documentary Otaku Unite announced, Robotech is one of the most controversial anime series of all-time (Bresler 2004). This stems from the fact that from the moment Macek shared his process of altering the original Japanese animated series into one American-released series, several fans issued verbal and written threats against his life. This essay explores this phenomenon of life imitating art via the fear/rejection of the hybrid of Japanese art and American rewriting by its own fan base.
Dana Sterling
Ariel/Marlene
In 1980s Japan, a struggle between the old guard, harmonious collective mentality and the idealism of the new breed of independent, rebellious youngsters became illustrated in anime. Three examples of Japanese animated series that televised this struggle were acquired, repackaged, rewritten, and rebroadcast in America by Carl Macek under the one name — Robotech. Robotech, the American TV series, is a hybrid in and of itself with its Japanese-created visuals married to an American-rewritten storyline. In addition to the show's own mixed heritage, Robotech contains multiple interracial and interspecies (human and alien) couples and hybrid offspring. This paper explores the hybrid nature of the American Robotech animated TV series and how the Eighties' generational struggle in Japan manifests itself through two hybrid, interspecies characters: Dana Sterling and Marlene/Ariel.
Synopsis written by Super Dimensional Analysis
This article proposes Robotech promotes interracial and interspecies breeding but rejects the offspring created from these unions. The article proposes the relationships of Max and Miriya and Bowie and Musica are evidence of promoting mixed marriages. It also points out a movement in 1980s Japanese culture of Shinjinrui which translates as new beings. While Japan is traditionally a homogeneous island nation with individuals working together collectively, the new generation living in 1982 rebelliously desired individuality. The article also references a change in 1980s Japanese youth culture of celebrating the gaijin or outsider as opposed to historically shunning this lifestyle. The first Robotech war worships Minmei as a culturally Chinese girl living in a Japanese society while Dana and Ariel are central hybrid characters of the second and third Robotech wars. This article suggests Lancer is also a gaijin of Shinjinrui culture. Another theme of Robotech proposed by this article is the concept of the middle generation which is defined as a child of parents from different races or cultures. The racially mixed child must balance the struggles between their two cultures. The middle generation is sometimes rejected by the culture of each parent as the offspring from their union is not purely one or the other but a combination of the two. Dana and Ariel are examples of this struggle.
Post-publication Peer Review by Super Dimensional Analysis
Interestingly, the paradigm Mr. Mich utilizes to explore the gaijin of Shinjinrui culture at the microcosm level of individual characters can also be applied to the macrocosm overview of Robotech and its three original Japanese source materials. Mr. Mich's proposed concept can be applied to individuals as well as the fictional societies they inhabit. In the first Robotech war, or Super Dimension Fortress Macross, the multicultural forces of Earth defeat the monocultural gender segregated enemy clone antagonists. In the second Robotech war, or Super Dimension Cavalry Southern Cross, the multicultural forces of Earth (Glorie) defeat the monocultural hive-mind enemy clone antagonists. In the third Robotech war, or Genesis Climber MOSPEADA, a collection of misfits defeat the monocultural hive-mind enemy clone antagonists. The protagonists of each of these series can be viewed as the gaijin of Shinjinrui culture proving victorious over antagonists which are thinly veiled analogies for the traditional Japanese cooperative collective old guard. Returning to the microcosm level of the individual, the societies of the antagonists also contain rebellious characters. These rebellious characters are some Zentreadi, Musica, Zor Prime, Sera, and Ariel. They all abandon their societies and choose micronian culture.
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A blog titled Spores, Molds, and Fungus posted a somewhat related essay written by username Incisivis on 11/26/2011. The essay is titled "A Discussion of Post-Super Dimension Fortress Macross Zentradi and Peace Children Characters." However, it relates to the entire Macross franchise and not Robotech. The essay is linked to below. The link was active as of 11/19/2019.
https://incisivis.livejournal.com/484259.html


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A Week 'til SharePoint 2010
Published: September 23rd, 2010
- David Rubinstein
Seven days until SharePoint 2010 makes its official debut. Despite so many having already seen so much of the new software, there is still plenty of excitement surrounding it. But hey, a launch can only mean one thing: It's party time!!
I, for one, will be thrilled when SharePoint 2010 makes it into wide release. I've been covering software launches of all types for more than 10 years, and can't recall as much hype surrounding a release as we've seen around SharePoint 2010. Perhaps it's just that this is a very vocal community of users, and that it's exciting for folks to be on board with software that's still on an upward curve. (It's become fashionable for folks in the community to note that they've been working with SharePoint since it was Site Server, or to say they began with Tahoe.)
SharePoint 2010, from all appearances, is a major improvement over MOSS 2007. But few think it's as significant an upgrade as MOSS 2007 was over the 2003 edition. The wide release will also mark the end of speculation about migration to 2010; we'll actually get to see how many folks move off their 2007 implementations, and how many don't.
The "SharePoint Shepherd" Robert Bogue reports he's well on his way to creating the next version of his seminal book, "The SharePoint Shepherd's Guide for End Users," with a target release date of mid June. To make the version even better, he's soliciting community input.
In a note, he wrote: "We'd love to hear about either the SharePoint 2007 tasks that you or the users you work with are commonly needing to remember. Or, if you've had time to spend with SharePoint 2010, we'd love to hear about key tasks, concepts or areas that you believe will be critical to users being able to effectively use the 2010 version of SharePoint. Any thoughts that you can share about the challenges you've been having with getting your users to be effective are welcome as well."
Robert says he'll send a complimentary copy of the 2007 book—or the 2010 book when available—to the 10 best responses. Send your input to me at drubinstein@bzmedia.com; we'll forward them to Robert and publish the best ones here as well!
About David Rubinstein
David Rubinstein is editor-in-chief of SD Times.
View all posts by David Rubinstein