- Open Access
Involvement of claudin-7 in HIV infection of CD4(-) cells
© Zheng et al; licensee BioMed Central Ltd. 2005
- Received: 07 September 2005
- Accepted: 20 December 2005
- Published: 20 December 2005
Human immunodeficiency virus (HIV) infection of CD4(-) cells has been demonstrated, and this may be an important mechanism for HIV transmission.
We demonstrated that a membrane protein, claudin-7 (CLDN-7), is involved in HIV infection of CD4(-) cells. A significant increase in HIV susceptibility (2- to 100-fold) was demonstrated when CLDN-7 was transfected into a CD4(-) cell line, 293T. In addition, antibodies against CLDN-7 significantly decreased HIV infection of CD4(-) cells. Furthermore, HIV virions expressing CLDN-7 on their envelopes had a much higher infectivity for 293T CD4(-) cells than the parental HIV with no CLDN-7. RT-PCR results demonstrated that CLDN-7 is expressed in both macrophages and stimulated peripheral blood leukocytes, suggesting that most HIV virions generated in infected individuals have CLDN-7 on their envelopes. We also found that CLDN-7 is highly expressed in urogenital and gastrointestinal tissues.
Together these results suggest that CLDN-7 may play an important role in HIV infection of CD4(-) cells.
- Human Immunodeficiency Virus
- 293T Cell
- Human Immunodeficiency Virus Infection
- Enhanced Green Fluorescent Protein
- LNCaP Cell
Human immunodeficiency virus (HIV) transmission through sexual intercourse accounts for the majority of infections. It must cross the epithelium during transmission, because the primary targets for HIV infection, CD4(+) cells, are protected by epithelial lining. However, the mechanism by which the virus transverses the epithelia covering the reproductive tract, the oral cavity, the gastrointestinal tract, or other tissues during viral transmission is poorly understood. This is an important question to investigate, because the epithelium, which is composed of stratified CD4(-) epithelial cells, protects the interface between host and environment (e.g., urogenital, gastrointestinal tract) or between organs and fluid spaces (prostate, kidney).
HIV may not utilize the mechanism of binding between gp120 on virions and CD4 molecules to infect epithelial cells, because these cells are CD4(-). One possible mechanism is that HIV utilizes lesions in the mucosal surface to invade underlying lymphoid cells [1, 2]. Conversely, it has been shown that lesions need not be present for the virus to cross the epithelial barrier [3–5]. Therefore, it is likely that HIV can penetrate epithelial layers by other mechanism(s). HIV may enter epithelial cells by a simple in-and-out means  or by transcytosis , whereby the cells passing across are not infected. However, recent reports demonstrate that many types of epithelial cells can be infected with HIV-1 [8–12], and that viral replication also occurs in infected epithelial cells.
Two possible mechanisms by which HIV infects CD4(-) cells have been proposed. Some reports suggest that the HIV gp120 surface glycoprotein binds to galactosylceramide (GalCer) [13–15] or chemokine receptors, including CXCR4 and CCR5, on the surface of CD4(-) cells [15–19], and that this binding initiates HIV entry into CD4(-) cells. Therefore, gp120 would be a key protein for HIV infection of CD4(-) cells. However, our previous results demonstrated that HIV infects many types of CD4(-) cells, some without surface gp120 [20–22]. Therefore, CD4(-) cell infection can be gp120-independent; i.e., the presence of gp120 glycoprotein molecules on the viral surface is not crucial for CD4(-) cell infection.
An important approach to understanding gp120-independent HIV infection is to identify the elements involved in this mechanism of infection. To do so, we compared a CD4(-) cell line that is highly susceptible to HIV infection to another cell line that has low susceptibility. By screening membrane proteins that are specifically expressed in the cell line highly susceptible to HIV, it is possible to identify the genes that are involved in HIV infection.
Our previous studies demonstrated that HIV efficiently infects the prostate cancer cell line, LNCaP . When a viral load of approximately 100 ng p24 was used for infection of 104 cells in culture, approximately 3–20% of LNCaP cancer cells were infected. The concentration of 100 ng p24/0.5 ml is similar to the viral load found in patients in the acute phase of infection. Infection of LNCaP cells is gp120-independent, because HIV with or without gp120 on its envelope is equally infectious for these cells, and antibodies against gp120 do not block infection. It is expected that certain proteins specifically expressed on the surface of this cell line are responsible for gp120-independent HIV infection.
We used subtractive cDNA cloning to identify a gene specifically expressed in LNCaP cells but not in the 293T and HeLa cell lines, which are not susceptible to HIV infection . Here we characterize the role of this protein, claudin-7 (CLDN-7), in gp120-independent HIV infection.
As previously described , we generated Env(-) HIVNL4-3 by deleting a fragment of 581 bp from the env coding region. This deletion truncates the gp120 envelope protein and introduces a frameshift into downstream gp41, thereby abrogating gp120 and gp41. The modified HIV also contains a reporter gene, the enhanced green fluorescent protein (EGFP). Insertion of the EGFP gene enables direct and sensitive detection of HIV infection. Previous reports have demonstrated that the substitution of the nef gene with EGFP does not alter viral infectivity [23–25]. To examine gp120-independent infection, gp120 and gp41 were deleted from the HIVNL4-3 genome, which eliminates the interference of viral envelope proteins. We have successfully utilized this modified viral strain to study gp120-independent infection, and therefore used this strain for the studies described herein [20, 22].
Our previous studies demonstrated that a membrane protein, claudin-7 (CLDN-7), is expressed in the HIV-susceptible cell line, LNCaP, but not in the HIV non-susceptible cell line, 293T . We studied the relationship of the expression of this protein and infection by HIV. In the described study, we transfected 293T cells with cloned CLDN-7, then characterized the infection of these cells with EGFP-modified HIVNL4-3.
The prostate cell line, LNCaP, is highly susceptible to gp120-independent HIV-1 infection
To accurately compare the infectivity for LNCaP and HeLa-CD4 cells by HIVNL4-3 containing the EGFP gene, we infected these two cell lines with different concentrations of virus (Figure 1C). When LNCaP cells in 24-well plates were infected with 50 pg of p24 counts of virus, less than five infected colonies per well were detected. When the cells were infected with virus containing 15 pg of p24, no infected colonies were detected. When HeLa-CD4 cells were infected with virus at similar or lower concentrations, we found that they could be infected by virus containing 15 pg of p24. However, when the concentration of virus was diluted to 5 pg of p24, no positive colonies were detected in the infected cell cultures, suggesting that the sensitivity of LNCaP cells for HIV is approximately 3-fold lower compared with that of HeLa-CD4 cells (Figure 1C).
To ensure that infection of LNCaP cells by virus generated from 293T cells is not caused by potential contamination of viruses that can modify the HIV envelope (e.g., amphotropic murine viruses), we tested 293T cells derived from various sources. The results were similar to those shown in Figure 1A, with much higher infectivity for LNCaP cells as compared to other cell lines, including 293T, HeLa, and DU145. It is unlikely that all of the 293T cells from different sources were contaminated; in other words, it is unlikely that the virus generated from 293T cells is modified by any contaminated amphotropic viruses.
CLDN-7211 or CLDN-7158 increases susceptibility of CD4(-) cells to HIV infection
Antibodies specific to CLDN-7 block gp120-independent infection
We also tested a preparation of polyclonal antibodies we generated against a peptide with the sequence CVTQSTGMMSCKMYD. The peptide sequence corresponds to aa positions 44 to 58 of CLDN-7. A cell-labeling assay demonstrated that this antibody preparation is able to bind CLDN-7 on the cell membrane (data not shown). However, it did not significantly block HIV infection of LNCaP cells, suggesting that this sequence region in CLDN-7 may not be essential for HIV infection (Figure 3B).
Increased infectivity for viruses generated with CLDN-7211 or CLDN-7158 on their envelopes
We also used EGFP-modified HIVJRCSF, a patient-derived R5 strain, to infect CD4(-) cells. Using co-transfection, we generated CLDN-7-modified HIVJRCSF from 293T cells. Because both CLDN-7-negative and -positive HIVJRCSF did not infect 293T cells, we infected another CD4(-) cell line, PC-3. The results demonstrated that CLDN-7 also significantly increases HIVJRCSF infectivity for this CD4(-) cell line.
Expression of CLDN-7 mRNA in peripheral blood lymphocytes and macrophages
Expression of CLDN-7 in other tissues
Results from our previous studies and others have revealed that CD4(-) cells can be infected by HIV, so it is important to understand this process in the context of viral transmission, whereby HIV transverses CD4(-) epithelial cell layers and infects CD4(+) T-lymphocytes and macrophages. In addition, infected CD4(-) cells, such as cells in the central nervous system, may serve as viral reservoirs. Some reports demonstrated that the binding of gp120 to GalCer or chemokine receptors is the mechanism of CD4(-) cell infection; however, only particular types of HIV were reported to infect certain types of CD4(-) cells [13–19]. Our previous studies demonstrated that both the X4 and R5 types of HIV can infect CD4(-) cells [20–22], and for many types of CD4(-) cells, gp120 is not required for infection.
Our results demonstrated that Env(-) HIV is still able to infect many types of cells via a gp120-independent mechanism. Our results demonstrated that although Env(-) HIV could not efficiently infect CD4(+) cells, it has similar infectivity for CD4(-)cells. It is possible that in some infected cells, HIV can down-regulate the expression of Env proteins to evade the immune response. If that were the case, there should be a high percentage of Env(-) HIV present in patients, which may be able to infect some types of CD4(-) cells, such as neurons and glial cells. The infection of brain cells may be a major hindrance of viral eradication because they have a long life-span,.
Because many tissues of the gastrointestinal and urogenital systems express the CLDN-7 gene, the cells in these tissues may be more susceptible to HIV-1 infection. These results are consistent with clinical data, with HIV-1 infection of epithelial cells of the oral mucosa, colon, intestine, and kidney being reported in patients [10, 14, 28–33]. In addition, because the virus uses a patch of cellular membrane as its envelope, when the virus is generated from cells in which the CLDN-7 protein is expressed, the virus also expresses this protein on its envelope. The presence of CLDN-7 molecules on the viral envelope may greatly increase its capacity for infecting other CD4(-) cells. It is expected that the viruses generated from infected PBL, macrophages, colon, intestine, trachea, kidney, lung, and prostate express this protein on their envelopes. This portion of the virus may have greater infectivity for CD4(-) cells compared to HIV virions that do not have CLDN-7 on their envelopes.
Our previous studies demonstrated that HIV can also use a gp120-independent mechanism by which to infect CD4(+) cells . Because macrophages express much lower levels of CD4 molecules on the cell surface, it is expected that expression of CLDN-7 on the surface of macrophages may help HIV to infect these cells.
Our results demonstrate that the presence of CLDN-7 on the surface of target cells increases viral susceptibility. Because CLDN-7 is expressed in organs related to HIV transmission and HIV pathogenicity (including the colon, kidney, lung, uterus, and oral tissue), it is expected that this protein is associated with HIV infection of CD4(-) cells in these organs, and is related to viral transmission or pathogenicity. Our results also demonstrated that virus generated from CLDN-7-transfected 293T cells has two- to 100-fold higher levels of infectivity, suggesting that the presence of CLDN-7 or other types of cellular membrane proteins on the viral envelope is important for viral infection. Because CLDN-7 is expressed in activated PBL and macrophages, and these two types of cells serve as HIV hosts, it is very likely that most HIV particles carry CLDN-7 on their surface. Therefore, it is very likely that this protein plays important roles in HIV infection of CD4(-) cells in humans.
Cell lines LNCaP, DU145, HT1080, R11, HeLa, CEM, and 293T were purchased from American Type Culture Collection (ATCC) or from other laboratories, as described [20, 22]. Cell lines LNCaP, PC-3, and DU145 are derived from the prostate, 293T from the embryonic kidney, CEM is a CD4(+) T-lymphocyte cell line, R11 is a renal carcinoma cell line, HT1080 is a fibroblast cell line, and HeLa is a from cervical cancer cell line. We also prepared HIV from an oral epithelial cell line derived from a patient. All cell lines were maintained in RPMI medium supplemented with 10% fetal bovine serum (FBS).
The CLDN-7 gene
Using a subtractive hybridization method combined with RT-PCR, followed by screening prostate cDNA libraries, we obtained three full-length cDNA clones. Sequence analysis demonstrated that these cloned cDNA sequences are homologous to human CLDN-7. Two of these three cDNA clones encode a peptide of 211 amino acid residues identical to that in Genbank. The third encodes a peptide of 158 amino acid residues, which is a truncated form of CLDN-7 lacking 53 amino acid residues at the C-terminus . Previous studies have demonstrated that both the full-length (CLDN-7211) and the truncated (CLDN-7158) forms of CLDN-7 are highly expressed in LNCaP but not 293T cells, and are expressed at low levels in HeLa cells . Both isoforms of CLDN-7 were inserted into a plasmid vector downstream of the CMV promoter.
Viral preparation and titration
To obtain HIV-1 Env(-) virus, we transfected either the 293T cell line or an oral epithelial cell line established in our laboratory with plasmid pNL4-3-EGFP-Env(-), which contains a modified HIVNL4-3 viral genome . The modified HIV-1NL4-3 genome has deletions in env (581 bp) and nef (222 bp), and insertion of the EGFP gene, as previous described . At 16 hours post-transfection, medium containing the plasmid was removed from transfected cell cultures. The transfected cell cultures were then washed with serum-free medium before adding new culture medium supplemented with 10% FBS. The medium containing virus was collected at days 2, 3, and 4 post-transfection. To remove cell debris, all the viral preparations were passed through a 0.2-micron filter. The collected viral stocks were titrated by p24 assays. The human 293T cell line does not express CLDN-7. Therefore, virus generated from this cell line is CLDN-7-negative. CLDN-7-positive virus was generated by co-transfection of 293T cells with both pCDNA3.1-CLDN-7 (CLDN-7211 or CLDN-7158) and the modified pNL4-3-EGFP-Env(-). Viruses generated from these co-transfections carried the CLDN-7 protein on their envelopes and were also titrated by p24 assays.
EGFP gene-modified HIVJRCSF, a patient-derived R5 strain, was constructed using a similar approach. A part of the nef gene was substituted by the EGFP gene. We generated infectious HIVJRCSF by transfection of 293T cells. This virus can infect cells that express both CCR5 and CD4 on the cell surface, and replicates in infected cells. Because it contains a viral genome that is almost intact but lacks the nef gene, this virus alone propagates in CCR5(+)/CD4(+) cells.
Infection of cell cultures
Cells (5 × 103) were plated into each well of 24-well plates 24 hours prior to infection. During infection, a viral aliquot with a p24 count of 100 ng was added into each well of cell cultures. The final volumes in each well were adjusted to 0.5 ml so that the concentration of virus was 100 ng of p24 counts of virus in 0.5 ml of medium. At 16 hours post-infection, the cell cultures were washed.
Liposome FUGENE-6 (Roche Molecular Biochemicals, Indianapolis, IN) was used to transfect the CLDN-7 plasmid into 293T cells. Cells (2 × 104) were plated into each well of 24-well plates 16 hours prior to lipofection. Plasmid DNA (2.0 μg) was mixed with FUGENE-6 liposome in 50 μl of RPMI medium for 10 minutes at room temperature before addition to cell cultures. At 8 hours [post-transfection?], the cell cultures were washed once and fresh medium then added.
Determination of EGFP expression
The expression levels of EGFP were determined by counting EGFP- positive cells by fluorescent microscopy or by fluorescent-activated cell sorting (FACS).
Cell culture medium from transfected 293T cells with pCDNA3.1-CLDN-7 and pNL4-3-EGFP-Env(-) or only pCDNA3.1-CLDN-7 was collected two to four days post-transfection. The collected medium was ultracentrifuged at 16,000 rpm for one hour at 4°C. The pellets were resuspended with 50 μl of protein lysis buffer (0.5% NP40, 1.0% glycerol, 0.1% β-mercaptoethanol, 40 mM Tris, pH6.8). The viral lysates were incubated at 37°C for 5 minutes before SDS-polyacrylamide gel electrophoresis (PAGE). Protein concentrations were determined by a standard protein assay (BioRad, Hercules, CA). Aliquots representing 2.5 μg of protein were separated by SDS-PAGE and transferred to a nylon membrane (Poly Screen PVDF; Fisher Scientific, Pittsburgh, PA). Polyclonal antibodies specific to human CLDN-7 (Zymed Laboratories, San Francisco, CA) were used according to the manufacturer's instructions to bind CLDN-7. The specificity of the CLDN-7 antibodies was tested by binding proteins isolated from CLDN-2 gene-transfected cells. No cross-binding was detected, although strong expression of CLDN-2 was noted when using CLDN-2-specific antibodies that were purchased from Zymed, indicating that those antibodies are highly specific.
Polyclonal antibodies against gp120 or gp160 were obtained from the NIH HIV Reagents Program (Rockville, MD), and gp41-specific monoclonal antibody (mAB) was obtained from Virogen (Watertown, MA). Polyclonal antibodies against CLDN-7 were purchased from Zymed Laboratories (0.25 mg/ml) or made from rabbits using a peptide of extracellular domain 1 of CLDN-7 with the sequence CVTQSTGMMSCKMYD, from position 54 to 68 (concentration 0.85 mg/ml). The homology of the amino acid sequence of this peptide is 73% or less of he corresponding sequences of other human claudins. Antibodies were added into both viral stocks and cell cultures for 10 minutes prior to infection at room temperature. The final concentration of antibodies in the infection medium was a 1:100 dilution. Four hours post-infection, the cell cultures were washed once, and fresh culture medium added. Virus with no antibody (control) was also added and incubated at room temperature for 10 minutes prior to infection.
We used the quanidinium thiocyanate method to isolate RNA. RNA isolated from approximately 105 cells was suspended in 20 μl of water. The isolated RNA was reverse transcribed, using AMV reverse transcriptase from Roche with oligo-dT as the primer. An aliquot of the cDNA was used for RT-PCR with primers 5'-CTCCTCTGACTTCAACAGCG and 5'-TGTTGCTGTAGCCAAATTCG to detect glyceraldehydes-3-phosphate dehydrogenase (GAPDH) cDNA. The primers of CLDN-7 have been previously described . The expected sizes of the PCR products were 121 bp (GAPDH) and 252 bp (CLDN-7211).
We thank Wendy Aft for editing. This work was supported by a grant from the National Institute of Health R01 AI047722 and The James Pendleton Charitable Trust.
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