- Open Access
The role of cholesterol and sphingolipids in chemokine receptor function and HIV-1 envelope glycoprotein-mediated fusion
© Ablan et al; licensee BioMed Central Ltd. 2006
- Received: 19 December 2006
- Accepted: 22 December 2006
- Published: 22 December 2006
HIV-1 entry into cells is a multifaceted process involving target cell CD4 and the chemokine receptors, CXCR4 or CCR5. The lipid composition of the host cell plays a significant role in the HIV fusion process as it orchestrates the appropriate disposition of CD4 and co-receptors required for HIV-1 envelope glycoprotein (Env)-mediated fusion. The cell membrane is primarily composed of sphingolipids and cholesterol. The effects of lipid modulation on CD4 disposition in the membrane and their role in HIV-1 entry have extensively been studied. To focus on the role of lipid composition on chemokine receptor function, we have by-passed the CD4 requirement for HIV-1 Env-mediated fusion by using a CD4-independent strain of HIV-1 Env.
Cell fusion mediated by a CD4-independent strain of HIV-1 Env was monitored by observing dye transfer between Env-expressing cells and NIH3T3 cells bearing CXCR4 or CCR5 in the presence or absence of CD4. Chemokine receptor signaling was assessed by monitoring changes in intracellular [Ca2+] mobilization induced by CCR5 or CXCR4 ligand. To modulate target membrane cholesterol or sphingolipids we used Methyl-β-cyclodextrin (MβCD) or 1-phenyl-2-hexadecanoylamino-3-morpholino-1-propanol (PPMP), respectively. Treatment of the target cells with these agents did not change the levels of CD4 or CXCR4, but reduced levels of CCR5 on the cell surface. Chemokine receptor signalling was inhibited by cholesterol removal but not by treatment with PPMP. HIV-1 Env mediated fusion was inhibited by >50% by cholesterol removal. Overall, PPMP treatment appeared to slow down the rates of CD4-independent HIV-1 Env-mediated Fusion. However, in the case of CXCR4-dependent fusion, the differences between untreated and PPMP-treated cells did not appear to be significant.
Although modulation of cholesterol and sphingolipids has similar effects on CD4 -dependent HIV-1 Env-mediated fusion, sphingolipid modulation had little effect on CD4-independent HIV-1 Env-mediated fusion. Chemokine receptor function remained intact following treatment of cells with PPMP. Therefore such treatment may be considered a more suitable agent to inhibit CD4 dependent HIV-1 infection.
- Chemokine Receptor
- NIH3T3 Cell
- Sphingolipid Metabolism
- Cholesterol Removal
- NIH3T3 Cell Line
HIV-1 delivers its genetic material into the cell by direct fusion of the viral membrane with the plasma membrane of the host cells . HIV-1 Env encodes a polypeptide (gp160) that is folded in the endoplasmic reticulum into a complex, disulphide-linked structure, which is anchored in the membrane by virtue of the hydrophobic, membrane-spanning domain in the gp41 moiety. During post-translational processing, the precursor glycoproteins oligomerize and are extensively glycosylated before cellular proteinases cleave the precursor at a characteristic sequence to create the mature glycoproteins gp120 and gp41. The surface glycoprotein, gp120, forms trimeric spikes, which are associated by non-covalent interactions with each subunit of the membrane-anchored gp41.
The triggering mechanisms that activate Env are quite complex involving target cell CD4  and chemokine receptors CCR5 and CXCR4 . The current data support a two-step model for receptor engagement that involves initial interactions between gp120 and CD4, followed by conformational changes in Env, which permit interaction of the gp120-CD4 complex with co-receptor leading to a further barrage of conformational changes that eventually lead to gp41 6-helix bundle formation and fusion . Receptors in membranes are not randomly distributed and lipids can play an important role in choreography of receptors . Therefore it stands to reason that modulation of lipid composition may affect the HIV-1 Env-mediated fusion reaction by altering the two-step choreography of CD4 and chemokine receptors required for HIV-1 entry. Based on this hypothesis a plethora of publications have appeared indicating that lipid modulation may have an indirect effect on HIV-1 entry/fusion by interfering with the choreography of CD4 and co-receptors (for reviews see [9, 10].
In order to further examine the effect of lipids on HIV-1 entry we asked the question whether similar lipid modulation would affect HIV-1 entry/fusion when we consider just one receptor required for entry. We addressed these issues by performing studies with CD4-independent HIV-1 Envs whose chemokine receptor-binding site is exposed without prior interaction with CD4. Hoxie and coworkers derived a variant of HIV-1/IIIB, termed 8x, which acquired the ability to utilize CXCR4 without CD4 . Moreover, when the V3 loop of a CCR5-tropic Env was substituted for its counterpart in the 8x Env, the resulting chimera (8xV3BAL) was found to utilize CCR5 but remained CD4 independent . We have used these constructs to further explore the role of target membrane cholesterol and glycosphingolipids in HIV-1 Env-mediated fusion.
Removal of cholesterol
Modulation of sphingolipid metabolism
Effects of PPMP treatment on HIV-1 Env-mediated fusion
Effects of cholesterol and PPMP treatment on chemokine receptor function
The two-step model for HIV-1 Env-mediated fusion  led to the notion that it is possible to interfere with the two receptor choreography by re-arranging the dance floor. The notion that cholesterol plays a key role in the maintenance of membrane organization  has led to a plethora of studies on the role of cholesterol in HIV-1 entry [10, 13, 18, 21–31]. It has been hypothesized that lipid raft domains  serve as sites that facilitate receptor interactions and signalling processes, and promote the cooperative event of HIV fusion. However, a role for rafts in HIV-1 entry has been called in question since CD4 mutants that localize this HIV-1 receptor to non-raft domains are perfectly capable of supporting HIV-1 entry [26, 27]. In this study we show that removal of cholesterol leads to inhibition of the one-step mode of HIV-1 Env fusion mediated by a CD4-independent strain of HIV-1 (Figure 2). The crucial step is the attachment of HIV-1 gp120 with CXCR4 or CCR5 inducing a barrage of conformational changes in HIV-1 Env, which leads to HIV-1 gp41 six helix bundle formation and fusion. Nguyen and co-workers have shown that maintenance of proper levels of cholesterol in the membrane is essential for chemokine binding and the conformational integrity of CCR5  as well as CXCR4 . Our data on the effects of cholesterol removal on signalling of CCR5 and CXCR4 (Figure 6) are consistent with those results. Therefore, the most straightforward explanation for our data showing inhibition of CD4-independent HIV-1 Env mediated fusion by cholesterol removal is that the conformational integrity of CCR5 and CXCR4 is impaired by this treatment. Therefore, their efficiency in grabbing HIV-1 gp120 and inducing the barrage of conformational changes in HIV-1 Env necessary for fusion has severely been reduced.
The situation with PPMP , which inhibits the synthesis of GlcCer, the precursor for glycosphingolipids synthesis, is somewhat more complex. Our initial hypothesis was that glycosphingolipids play a role in HIV-1 entry/fusion. Therefore, a reduction of glycosphingolipid levels by blocking their synthesis would adversely affect HIV-1 fusion. However, glycosphingolipids-deficient cells lines, which were engineered to express HIV-1 receptors, were highly susceptible to HIV-1 Env-mediated fusion  suggesting little or no involvement of glycosphingolipids in fusion of cells expressing high levels of HIV-1 receptors. However, PPMP has a number of different effects on sphingolipid metabolism, which include an increase of ceramide levels [33, 34]. Zimmerberg and co-workers performed a very detailed study on the effects of PPMP-treatment of cells on the membrane distribution of influenza hemagglutinin . Fluorescence spectroscopy indicated that such treatment alters the relative distance and orientation of these membrane-embedded proteins on molecular scale (6–7 nm), and quantitative electron microscopy indicated relatively small effects on longer (≥ 20 nm) length scales. A similar study on CD4 and co-receptor distribution is beyond the scope of this study. However, CD4 has a similar domain structure as hemagglutinin (large extracytoplasmic domain, one membrane-spanning region, short cytoplasmic tail) and is also considered to be a "raft" protein . We may therefore surmise that PPMP treatment will exert a similar effect on CD4 distribution on the cell surface. On the other hand, the seven trans-membrane proteins CXCR4 and CCR5 may be less sensitive to such treatment as indicated by the Ca2+ signaling experiment (Figure 6). Therefore, the sensitivity to PPMP treatment in the CD4-independent setting may be less pronounced when a one-step mechanism is required to mediate HIV-1 Env fusion.
By reducing HIV-1 Env-mediated fusion to a one-step chemokine receptor- dependent process, we have shown that cholesterol plays a role in both CD4 and chemokine receptor-mediated steps, whereas modulation of sphingolipids only affects the choreography between the two steps. Chemokine receptor function remained intact following treatment of cells with PPMP. Therefore such treatment may be considered a more suitable agent to inhibit CD4 dependent HIV-1 infection.
Phycoerythrin (PE)-labeled Mabs against CD4, CXCR4 and CCR5 and their isotype controls were obtained from Pharmingen (San Diego, CA). The anti-GM3 Mab GMR6 was obtained from Seikagaku America (Falmouth, MA) and Cy3-conjugated anti-mouse Fab from Jackson Immunochemicals (West Grove, PA). Methyl-β-cyclodextrin (MβCD) and cholesterol/MβCD complexes purchased from Sigma (St. Louis, MI), and 1-phenyl-2-hexadecanoylamino-3-morpholino-1-propanol (PPMP) from Matreya, Inc. (Pleasant Gap, PA). Cholesterol in total cell lysate was determined using the Cholesterol Oxidase kit (Wako Chemicals USA Inc, Richmond, VA). The cytoplasmic dyes 5-chloromethylfluorescein diacetate (CMFDA), 5- and 6-([(4-chloromethyl)benzoyl]-amino)tetramethyl-rhodamine (CMTMR) and Fura-2 AM were from Molecular Probes (Eugene, OR). The chemokine receptor ligands SDF1-α and MIP1-β were from Peprotech (Rocky Hill, NJ). All other biochemicals used were of the highest purity available and were obtained from regular commercial sources.
Cells and viruses
NIH 3T3 cells constitutively expressing CD4 and/or CXCR4, and NIH 3T3 cells constitutively expressing CD4 and/or CCR5, were kindly provided by Dr. Dan Littman (New York University, New York). HIV-1 Env 8x and 8xV3BAL , kindly provided by Dr. Robert Doms, University of Pennsylvania, Philadelphia, were expressed on the surface of NIH3T3 cells by transfection using the vaccinia T7-polymerase (vTF7-3), which was obtained through the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH from Drs Tom Fuerst and Bernard Moss.
Surface expression of GM3, CD4 and chemokine receptors
The fluorescence of cells stained with PE-conjugated Mabs against CD4, CXCR4 and CCR5 was compared with the appropriate PE-conjugated isotype controls. Cell labeling with PE-conjugated Mabs was done in the presence of 2% serum, after which cells were washed and fixed with 1% paraformaldehyde. The analysis was performed on a FACStar plus flow cytometer. GM3 levels were monitored by immunofluorescence using the anti-GM3 Mab (GMR6) and a Cy5-stained antimouse Fab.
HIV-1 Env-mediated cell fusion
To express 8x or 8x-V3BaL gp120-gp41, NIH3T3 cells plated on T75 flasks were incubated with the vaccinia virus vTF7-3 (5 M.O.I.) for 1–2 hrs at 37°C. Subsequently, the cells were transfected with 15 μg DNA (psp73.8x or psp73.8x.V3BaL using lipofectamine (Invitrogen, Inc.) in 3 ml DMEM (without serum) and incubations were continued for 4–6 hrs at 37°C. DMEM containing 10% FBS + antibiotics (D10) was added and cells were incubated for additional 16–20 hours. For the fusion assay, cells were harvested using EDTA-based cell dissociation buffer (Life Technologies, Inc.) and labeled with 10 μM CMFDA following manufacturer's directions. The CMFDA-labeled HIV-1 Env-expressing cells (2 × 105 per well) were added to the same number of CMTMR-labeled NIH3T3 targets expressing CD4 and/or cognate co-receptors and the samples were incubated for 4–10 hrs at 37°C. Dye redistribution as a result of fusion was monitored microscopically as described previously . The extent of fusion was calculated as: Percent Fusion = 100 × number of cells positive for both dyes/number of bound cells positive for CMTMR.
Intracellular [Ca2+] mobilization was measured by incubating 2 × 107 cells/ml in loading medium (DMEM containing 10% FCS and 2 mM glutamine) with 7 mM Fura-2 AM for 45 min at room temperature. The dye-loaded cells were washed and resuspended in saline buffer (138 mM NaCl, 6 mM KCl, 1 mM CaCl2, 10 mM HEPES, 5 mM glucose, and 0.1% BSA, pH 7.4) at a density of 0.5 × 106/ml. The cells were then transferred into quartz cuvettes (1 × 106 cells in 2 ml saline buffer), which were placed in a fluorescence spectrometer (Perkin-Elmer, Beaconsfield, U. K.). Chemokines were added in a volume of 20 ml to each cuvette. The intensity of the fluorescence was measured as the ratio at 340 and 380 nm wavelengths and calculated using a FL WinLab program (Perkin-Elmer).
We are grateful to Dr Robert Doms for providing the 8x and 8xV3BAL plasmids, to Dr. Dan Littman for the NIH3T3 cells bearing CD4, CXCR4 and/or CCR5, and the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH for vaccinia T7-polymerase. The technical assistance by Ms. Wanghua Gong of SAIC-Frederick is acknowledged.
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