- Open Access
Inhibition of HIV-1 replication by small interfering RNAs directed against Glioma Pathogenesis Related Protein (GliPR) expression
© Capalbo et al; licensee BioMed Central Ltd. 2010
- Received: 22 August 2008
- Accepted: 31 March 2010
- Published: 31 March 2010
Previously, we showed that glioma pathogenesis related protein (GliPR) is induced in CEM T cells upon HIV-1 infection in vitro. To examine whether GliPR plays a role as HIV dependency factor (HDF), we tested the effect of GliPR suppression by siRNA on HIV-1 replication.
Induction of GliPR expression by HIV-1 was confirmed in P4-CCR5 cells. When GliPR was suppressed by siRNA, HIV-1 replication was significantly reduced as measured by HIV-1 transcript levels, HIV-1 p24 protein levels, and HIV-1 LTR-driven reporter gene expression, suggesting that GliPR is a cellular co-factor of HIV-1. Microarray analysis of uninfected HeLa cells following knockdown of GliPR revealed, among a multitude of gene expression alterations, a down-regulation of syndecan-1, syndecan-2, protein kinase C alpha (PRKCA), the catalytic subunit β of cAMP-dependent protein kinase (PRKACB), nuclear receptor co-activator 3 (NCOA3), and cell surface protein CD59 (protectin), all genes having relevance for HIV-1 pathology.
The up-regulation of GliPR by HIV-1 and the early significant inhibition of HIV-1 replication mediated by knockdown of GliPR reveal GliPR as an important HIV-1 dependency factor (HDF), which may be exploited for HIV-1 inhibition.
- Jurkat Cell
- Cellular Gene Expression
- Nuclear Receptor Coactivator
- Lymphocytic Cell Line
- Cell Surface Protein CD59
The replication of HIV-1 depends on specific host factors [1–4]. A recent report identified 273 cellular HIV-1 dependency factors (HDF), that are important for HIV-1 replication . Furthermore, HIV-1 modifies the mRNA expression of a relatively large number of host cell genes, as shown by several reports [6–10]. Differential display experiments suggested that the expression of ~700 host genes (approximately 3% of all cellular genes) is modified by HIV-1 infection in vitro . A microarray analysis using a limited subset of 1500 cDNAs identified 20 differentially expressed mRNAs from several cellular pathways . Specific HIV-1 proteins including Tat, Nef, gp120 and Vpr were examined to dissect their role in modifying the transcription of cellular genes [11–14]. While some of the differentially expressed cellular genes may play a role in host defense mechanisms, others may facilitate HIV-1 replication, infectivity, species propagation and survival. A subgroup of differential cellular gene expressions may even support both host defense and viral replication, since HIV-1 replication is linked to immune activation of CD4+ T cells. Due to evolutionary selection, HIV-1 is expected to induce specific host factors, favorable for viral replication or propagation, and to suppress unfavorable cellular gene products [15–17]. Therefore, the examination of host cell genes, that are up-regulated upon HIV-1 infection, is expected to identify potential targets for inhibition of HIV-1 replication.
Previously, we found an early up-regulation of GliPR expression by more than 5-fold in CEM T cells infected with HIV-1 by a differential display screen . Therefore, we were interested in delineating the role of GliPR for HIV-1 replication.
GliPR was identified originally in human glioblastomas  and was also described as related to testes-specific, vespid, and pathogenesis protein 1 (RTVP-1) . Increased expression of GliPR was associated with myelomonocytic differentiation in macrophages . Whereas GliPR has been reported to act as a tumor suppressor gene inducing apoptosis in prostate cancer [21–24], it appears to be an oncogene in glioblastomas  and Wilms tumors . RTVP-1 protein was reported to contain a N-terminal signal peptide sequence and a transmembrane domain . Furthermore, homology studies revealed a putative active enzymatic center in GliPR . GliPR is homologous to group 1 plant pathogenesis-related proteins (PR-1) that are implicated in plant defense responses to viral, bacterial, and fungal infection [28, 29]. Since GliPR shows structural similarities with its homologous plant PR-1 proteins, mammalian testis proteins (TPX1) and the insect venom Ag-5 protein, which are secretory proteins [29, 30], it has been suspected that GliPR is also secreted. GliPR's homology with plant PR-1 proteins that have been attributed with a defense function may raise the question whether GliPR has an evolutionarily conserved role in innate immune response and human host defense of viral infection including HIV-1. Alternatively or additionally, HIV-1 may induce and exploit GliPR for viral replication.
The effect of GliPR knockdown on HIV-1 replication was studied, in order to test the hypotheses of GliPR being a host defense protein against or a co-factor of HIV-1. Furthermore, in order to identify downstream targets of GliPR, the effect of GliPR suppression on cellular gene expression was also investigated using cDNA microarrays.
GliPR is induced upon HIV-1 infection in P4-CCR5 cells
Suppression of GliPR mediated by short interfering RNA
Viability and proliferation rate of P4-CCR5 cells transfected with siRNAs against GliPR or with the non-silencing siRNA remained unchanged as determined by WST-1 cell proliferation assay (Fig. 2b).
In order to establish a test system in a T cell line as well, a predominant type of host cell for HIV-1, Jurkat cells were transfected with 2 different siRNAs targeting GliPR, control non-silencing siRNA, or mock transfection without any siRNA. GliPR mRNA expression was reduced by around 64% to 69% at 48 hours after transfection with specific siRNAs compared to controls (Fig. 2c). The less pronounced reduction of GliPR expression compared to P4-CCR5 HeLa cells may be attributed to the lower transfection efficiency generally observed in T cell lines. In this experiment, approximately 70% of Jurkat cells were transfected, while 90% of P4-CCR5 HeLa cells were transfected.
In general, GliPR-directed siRNAs reduced the expression of GliPR effectively in P4-CCR5 and Jurkat cells without affecting cell viability.
Down-regulation of GliPR by siRNA inhibits HIV-1 replication in P4-CCR5 and Jurkat cells
The effect of GliPR suppression on HIV-1 replication was confirmed by p24 ELISA, showing a significantly reduced p24 expression at day 4 post infection in cultures with GliPR knock-down compared to controls with non-silencing siRNA (Fig. 3c).
In order to test this phenomenon in T cells, Jurkat cells transfected with siRNAs specific to GliPR or control siRNA were infected with HIV-1 at a MOI of 0.01. GliPR-specific siRNAs resulted in a significant reduction of HIV-1 replication, similar to the positive control with siRNA against p24 (Fig 3d). Thus the T cell line results are in line with the data in P4-CCR5 cells.
These results demonstrated that siRNA-mediated suppression of GliPR inhibited HIV-1 replication implicating that GliPR promotes HIV-1 replication. It was not possible to employ the opposite approach by assessing the effect of GliPR's over-expression on HIV-1 replication, since forced expression of GliPR caused rapid induction of apoptosis in HeLa cells and Jurkat cells (unpublished data).
Differentially expressed genes after GliPR suppression with relevance for HIV-1 replication
Differentially expressed genes in siGliPR transfected HeLa cells relevant to HIV-1 pathology.
Probe Set ID
protein kinase, cAMP-dependent, catalytic β
nuclear receptor coactivator 3
syndecan 2 (heparan sulfate proteoglycan)
CD59 antigen p18-20
protein kinase C, alpha
The present investigation confirmed the up-regulation of GliPR induced by HIV-1 infection that we had found in a lymphocytic cell line  in P4-CCR5 HeLa cells. The suppression of GliPR expression by siRNA was associated with a significant inhibition of HIV-1 replication compared to controls as determined by quantitative PCR for HIV-1 transcripts, p24 ELISA, and HIV-1 LTR driven β-galactosidase expression. The inhibition of HIV-1 transcription following knockdown of GliPR was confirmed in Jurkat T cells. Furthermore, the knockdown of GliPR in uninfected HeLa cells revealed 6 differentially expressed genes, which had been reported to be associated with HIV-1 pathology.
The first hypothesis that GliPR induction is a cellular defense reaction hindering HIV-1 replication has to be questioned. If GliPR had exerted an anti-viral effect against HIV-1, the suppression of GliPR would have been expected to show an enhancing effect on HIV-1 replication, which was not found to be the case.
The second hypothesis that GliPR acts as a HIV-1 co-factor has to be favored, since down-regulation of GliPR expression caused a significant inhibition of HIV-1 replication, implying that GliPR promotes HIV-1 replication. This result could not be corroborated by the inverse technique of over-expressing GliPR because over-expression of GliPR caused apoptosis as reported for prostate cancer cell lines  and confirmed by us for HeLa and Jurkat cells (unpublished data). Apoptosis would have disguised a putative promoting effect on HIV-1 replication, since apoptosis per se would have affected the kinetics of HIV-1 replication.
The initiation of apoptosis in an infected cell may be considered to be an ancient defense mechanism aimed at the abortion of infection for the organism. Apparently, HIV-1 escapes this putative mechanism of defense as long as its replication has not been completed by blocking apoptosis initially via up-regulation of bcl-2 via Tat [32–34] or by other mechanisms, e.g. reduction of Bax or inhibition of ISG15 [35, 36].
Moreover, HIV-1 appears to exploit a specific function of GliPR or GliPR-induced gene products for its replication. Therefore, GliPR may be considered as an HDF [1–4]. A recent report identified 237 HDF in a broad siRNA screen, in addition to 36 already described HDF . GliPR was not found by this HDF screen, although our results suggest that it meets the criteria for an HDF. Apparently the detection of HDF depends on the specific experimental conditions and the selection criteria set for sensitivity and specificity of a screening approach.
It has been shown that tumor suppressor protein p53 is a direct transcriptional activator of GliPR. GliPR may also be induced independently of p53 . It has been reported that HIV-1 induces or activates p53 [37, 38], suggesting a p53-mediated pathway for up-regulation of GliPR by HIV-1.
It is also of interest to understand the mechanism by which GliPR promotes HIV-1 replication. The modeling of GliPR's protein structure revealed an active site . Protein Tex31, which is a member of the PR-1 protein family and a component of the cone snail venom, is a substrate specific protease . Golgi associated PR-1 related protein-1 (GAPR-1) also called GliPR2 due to its close homology with GliPR, is a putative serine protease, too . It may be hypothesized that a potential GliPR protease activity may be involved in the processing of a specific HIV-1 protein as it has been demonstrated for other cellular proteases such as furin and PC7 in processing of gp160 . The interaction of GliPR with HIV-1 polypeptides is possible since GliPR is localized in the endoplasmic reticulum (unpublished data).
Our microarray screen found 6 gene products down-regulated by GliPR suppression that have been reported in the context of HIV:
Syndecan-1 and syndecan-2 are heparansulfate proteoglycans and membrane proteins involved in cellular proliferation, migration and matrix interactions. Syndecan-1 functions as receptor for internalizing extracellular Tat protein  and syndecan-2 as regulator of T cell activation .
The catalytic subunit β of cAMP-dependent protein kinase (PRKACB) phosphorylates HIV-1 precursor protein and matrix protein p17 thereby initiating their translocation . PRKACB is incorporated in HIV-1 virions and regulates viral infectivity . PRKCA phosphorylates Tat and transactivates HIV-1-LTR .
The nuclear receptor coactivator 3 (NCOA3) interacts with Tat enhancing Tat's transactivating effect .
The cell surface protein CD59 (protectin) prevents the formation of membrane attack complexes (MAC). CD59 co-localizes with HIV-1 matrix protein p17 in virions .
GliPR is induced in early HIV-1 infection in vitro. According to the profound inhibitory effect of GliPR knock-down on HIV-1 replication, GliPR is an important HDF. Future research needs to address whether GliPR directly functions as a co-factor of HIV-1 processing or whether it exerts its effect via other cellular target genes as identified by our microarray screen. It is also important to define the role of GliPR in cellular defense against other viral infections in general.
Cell culture and HIV-1 infection
For siRNA knock-down experiments, HeLa cells and P4-CCR5  cells (HeLa CD4+ CCR5+ long terminal repeat-LacZ) were cultured in Dulbecco's modified Eagle's medium (Invitrogen, Karlsruhe, Germany). C8166 and Jurkat cells were cultured in RPMI 1640 medium (Invitrogen). All media were supplemented with 10% fetal calf serum (Gibco-BRL, Karlsruhe, Germany), 1% glutamine (Gibco-BRL) and 1% antibiotic solution (penicillin and streptomycin; Gibco-BRL). P4-CCR5 cells were cultured in the presence of 100 μg/ml G418 (PAA Laboratories, Coelbe, Germany) and 1 μg/ml Puromycin (PAA Laboratories). Transfection and infection of the cells were carried out in the absence of any antibiotics. The HIV-1 strain LAI was taken from the supernatant fluid of freshly infected H9 cells. Viral titer (TCID50 units/ml) was determined by titration on C8166 cells as described .
24 h after siRNA transfection, P4-CCR5 or Jurkat cells were infected with HIV-1LAI in triplicate at a multiplicity of infection (MOI) of 0.01 or 0.05. Infection of P4-CCR5 cells was carried out in the presence of 50 μg/ml DEAE-Dextran (Sigma, Taufkirchen, Germany). After incubation for 4 h the cells were washed with PBS and re-fed with fresh medium. Cells and supernatant samples were collected for quantitative PCR analysis, β-galactosidase enzyme assay and HIV-1 p24 antigen ELISA at indicated time points.
siRNAs with the following sequences were used: a positive control siRNA against HIV-1 p24 , (si-p24: 5'-GAU UGU ACU GAG AGA CAG Gdtdt-3'); a negative control non-silencing siRNA with no known homology to mammalian genes (si-nons-Rho: 5'-UUC UCC GAA CGU GUC ACG Udtdt-3'; 5-prime labeled with rhodamine); and two different siRNAs specific to GliPR (si-GliPR-1: 5'-GGU GAA ACC AAC AGC CAG Udtdt-3'; si-GliPR-2: 5'-GGA CUA UGA CUU CAA GAC Udtdt-3'). All siRNAs were synthesized by Ambion (Darmstadt, Germany) and were purchased as annealed RNA-duplexes. 24 h before transfection, HeLa or P4-CCR5 cells were plated in 24-well plates (Corning, Kaiserslautern, Germany) at 5 × 104 cells per well in Dulbecco's minimal essential medium containing 10% FBS with no antibiotics. Transfections were performed with Lipofectamine 2000 transfection reagent (Invitrogen) with siRNA at a final concentration of 20 nM according to the manufacturer's recommendations. After incubating for 6 h, the lipid/siRNA complexes were removed and replaced with fresh medium. For further analysis, cells were removed from the culture dish by trypsinization with 0.25% trypsin/0.02% EDTA in PBS (Cambrex, Verviers, Belgium) at different time points after transfection. Transfection of Jurkat cells was performed with HiPerFect Transfection Reagent (Qiagen, Hilden, Germany) with siRNA at a final concentration of 100 nM according to the manufacturer's recommendations. Transfection efficiency was analyzed by flow cytometry 24 h after transfection. Data were acquired and analyzed on FACScan with Cell Quest software (Becton Dickinson, Heidelberg, Germany). Effects on cellular viability after siRNA treatment were measured using the cell proliferation reagent WST-1 according to the manufacturer's instructions (Roche, Penzberg, Germany).
Real time PCR quantification of viral and cellular RNA
RNA was extracted using the RNeasy mini kit (Invitrogen) including treatment with RNase-free DNase I (Qiagen). Synthesis of cDNA was carried out using random hexamer primers and Superscript-II RNaseH-reverse transcriptase according to the manufacturer's specifications (Invitrogen).
Real-time PCR was performed in duplicate reactions employing ABI PRISM 7700 (Applied Biosystems, Darmstadt, Germany) with standard conditions (50°C for 2 min, 95°C for 10 min and 40 cycles at 95°C for 15 s and 60°C for 1 min). The 25 μl PCR included 2,5 μl cDNA, 1× TaqMan® Universal PCR Master Mix (Applied Biosystems), 0.2 μM TaqMan® probe, 0.2 μM forward primer and 0.2 μM reverse primer. Primers and probes were designed using Primer Express v.1.0 software (Applied Biosystems) and were synthesized by Thermohybaid (Ulm, Germany). In order to quantify GliPR, HIV-pol and GAPDH cDNA, the following primers and probes were used: GliPR (sense: 5'-TGC CAG ACA AAG CAT GCG T-3'; antisense: 5'-GCT GTG TGT GAA TAA TTG GAG ACA A-3'; probe: 5'-FAM-TCA CAC TTG CTA CAA TAG CCT GGA TGG TTT C-3'-TAMRA), HIV-pol (sense: 5'-AAT TTC ACC AGT ACT ACG GTT AAG GC-3'; antisense: 5'-CTT TAA TTC TTT ATT CAT AGA TTC TAC TAC TCC TTG-3'; probe: 5'-FAM-TGT TGG TGG GCG GGA ATC AAG C-3'-TAMRA) and GAPDH (sense: 5'-GAA GGT GAA GGT CGG AGT C-3'; antisense: 5'-GAA GAT GGT GAT GGG ATT TC-3'; probe: 5'-FAM-CAA GCT TCC CGT TCT CAG CC-3'-TAMRA). The probes were labeled with FAM at the 5' end and TAMRA at the 3' end. Copy numbers of the respective transcripts were calculated by plasmid standard curves, normalized by GAPDH housekeeping gene transcripts. Standard curves were obtained after amplification of log step dilutions between 10 to 106copy numbers of purified plasmids carrying the amplicons of GliPR, HIV-1-pol (modified plasmid pLAI.2 obtained from the NIH AIDS Research & Reference Reagent Program) or human GAPDH , respectively. The plasmid standard for the quantification of GliPR was prepared by inserting a PCR-generated fragment (sense: 5'-GGA TCC ATG CGT GTC ACA CTT GCT ACA ATA GC-3' and antisense: 5'-GTC GAC TTA GTC CAA AAG AAC TAA ATT AGG GTA CTT GAG C-3') into pCR2.1 (Invitrogen), which was amplified using HeLa cDNA as template.
β-Gal staining of cells
At indicated time points after HIV-1LAI infection, P4-CCR5 cells were washed twice with PBS and fixed for 5 min in fixative (0.25% glutaraldehyde in PBS) at room temperature. After two washes with PBS, cells were covered with staining solution (PBS containing 4 mM potassium ferrocyanide, 4 mM potassium ferricyanide, 2 mM MgCl2, and 0.4 mg/ml of X-Gal [5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside]) and incubated at 37°C. Subsequently plates were washed twice with PBS and numbers of β-Gal-positive (blue) cells were examined microscopically.
β-galactosidase enzyme assay
Cell lysates were prepared by using Reporter Lysis Buffer (Promega, Mannheim, Germany). To perform 96-well plate β-galactosidase assays 50 μl of cell lysates and 50 μl of 2× β-galactosidase assay buffer (Promega) were mixed and incubated at 37°C for 30 min. To stop the reaction, 150 μl of 1 M sodium carbonate was added to the mixture and mixed well by vortexing briefly. Absorbance of the reaction mixture was read immediately at 420 nm. A standard curve was created, using standards between 0 and 6.0 × 10-3 units of Galactosidase (Promega). Reporter assay results were normalized according to relative cell numbers, which were estimated by using the cell proliferation reagent WST-1 according to the manufacturer's instructions (Roche).
HIV-1 p24 antigen ELISA
HIV-1 p24 ELISA was performed using a commercially available kit (Beckmann Coulter, Krefeld, Germany) according to the manufacturer's instructions. For measuring p24 in the supernatants, 100-fold dilutions of the supernatants were used. All ELISA measurements were done in triplicate.
Gene expression analysis by microarrays
The microarray analysis of the effect of GliPR suppression by siRNA was performed using the HG-U133 Plus 2.0 microarray of Affymetrix (Santa Clara, CA USA) per manufacturer's instructions (GeneChip® Expression Analysis Manual). This chip contains 47,000 transcripts which represent 39,000 annotated genes. The data analysis was carried out according to established standards for Affymetric microarrays using GeneChip Operating Software (GCOS; Affymetrix) and GeneSpring (Agilent Technologies).
We are very grateful to Sandra Markovic for excellent technical assistance.
We are very grateful to the H. W. & J. Hector Stiftung (foundation), Mannheim, Germany that provided a grant to support this research.
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