Simian virus 40 inhibits differentiation and maturation of rhesus macaque DC-SIGN+-dendritic cells
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Dendritic cells (DC) are the initiators and modulators of the immune responses. Some species of pathogenic microorganisms have developed immune evasion strategies by controlling antigen presentation function of DC. Simian virus 40 (SV40) is a DNA tumor virus of rhesus monkey origin. It can induce cell transformation and tumorigenesis in many vertebrate species, but often causes no visible effects and persists as a latent infection in rhesus monkeys under natural conditions. To investigate the interaction between SV40 and rhesus monkey DC, rhesus monkey peripheral blood monocyte-derived DC were induced using recombinant human Interleukin-4 (rhIL-4) and infective SV40, the phenotype and function of DC-specific intracellular adhesion molecule-3 grabbing nonintegrin (DC-SIGN)+ DC were analyzed by flow cytometry (FCM) and mixed lymphocyte reaction (MLR). Results showed that SV40 can down-regulate the expression of CD83 and CD86 on DC and impair DC-induced activation of T cell proliferation. These findings suggest that SV40 might also cause immune suppression by influencing differentiation and maturation of DC.
KeywordsDendritic cell Simian virus 40 Rhesus monkey
Dendritic cells (DC) are the most prominent antigen presenting cells which play a pivotal role in the orchestration of the various forms of immunity and tolerance [1, 2]. The DC-SIGN+ dendritic cells (DDC), which were found in the interstitium of heart, liver, lung, kidney, skin, etc., are usually thought to play a pivotal role in the immunosuppressive induction of a number of pathogens [3, 4, 5, 6]. These pathogens include measles virus [7, 8, 9], human immunodeficiency virus [10, 11, 12], human hepatitis B virus [13, 14], Hepatitis C Virus , tubercle bacillus [16, 17], typhoid bacillus [18, 19], anthrax bacillus [20, 21], etc. Details of immune evasion of these pathogens are still unclear at present [22, 23]. Simian virus 40 (SV40) is a double-stranded DNA tumor virus that was first identified by Sweet in 1960 . SV40 can transform many types of cells and cause carcinogenesis in vitro, including those of human origin [25, 26, 27]. The virus is usually dormant and asymptomatic in rhesus monkeys under natural conditions. Whether SV40 subvert dendritic cell function remains unclear. The present study was designed to examine the effect of SV40 infection on DC-SIGN+ dendritic cells.
2. Materials and methods
Five- to ten-year-old female rhesus macaques were obtained from the Kunming National Primate Research Center of China. The SV40 large T antigen (LT-AG) gene fragment in rhesus monkey peripheral blood was tested using the forward primer (5'-AACAGCCC AGCCACTATAAGTACC-3', 3892~3869) and the reverse primer (5'-AGCAACTCCAGCCATCCATTC-3', 3642~3662). The expected PCR product is 251 bp. The SV40 major capsid protein VP1 gene fragment in rhesus monkey peripheral blood was detected using the following forward primer (5'-CTCAAATGG GCAATCCTGATG-3', 1665~1685) and the reverse pri mer (5'-CATAGCAGTTACCCCAATAACCTC-3', 1882~1859). The expected PCR product is 218 bp. Those rhesus monkeys that tested SV40-DNA fragment negative were selected to participate in this study.
2.2. Virus and cell
The reference strain SV40-776 was proliferated in Vero cells (ATCC, CCL-81) which were cultured in Minimum Essential Medium (MEM, GIBCO) containing 2% fetal bovine serum (FBS, GIBCO), 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin at 37°C, 5% CO2, 95% air and 100% relative humidity. Repetitive freeze-thaw cycles were used to lyse the cells and release intracellular virus particles when more than 75 per cent of the infected Vero cells show evident cytopathic effect (CPE). The supernatant of infected cells suspension, which was obtained by centrifuging the freshly thawed virus suspension at 1000 × g for 30 min at room temperature to remove any cell debris, was precipitated with 10% (wt/vol) polyethylene glycol 6000 in the presence of 0.5 M NaCl overnight at 4°C and centrifugation at 12,000 × g for 20 min at 4°C. The pellet was resuspended in 4 ml phosphate buffered saline (PBS, pH 7.2), and virus particles were purified by ultracentrifugation in a cesium chloride (CsCl) density gradient at 120,000 × g for 24 h at 20°C. The purified SV40 were divided into two parts, half of them was inactivated by β-propiolactone (BPL) with a final concentration of 0.01 M for 72 h at 4°C and then was settled at 37°C for 2 h to decompose BPL completely. The inactivated SV40 was stored at -20°C after demonstration of no infectivity. The other half was assayed for plaque forming units (pfu) of the purified SV40 and stored at -80°C until use.
2.3. Induction of rhesus macaque DC
Mononuclear cells were isolated from 3~5 ml SV40-negative rhesus monkey peripheral blood by Ficoll-Hypaque density gradient centrifugation. Monocytes were separated from lymphocyte by glass adherence, and proliferated by using RPMI 1640 medium (GIBCO) containing 10% FBS, 20 mM HEPES, 1 mM sodium pyruvate, 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin, 500 ng/ml recombinant human granulocyte-macrophage colony stimulating factor (rhGM-CSF, R&D Systems) at 37°C, 5% CO2, 100% relative humidity, and induced to differentiate toward IDC by using 10 ng/ml recombinant human interleukin-4 (rhIL-4, R&D Systems).
2.4. Isolation of T-Lymphocytes
T-lymphocytes were isolated from cell suspensions consisting of T cells and B cells with Nylon Fiber Column T (Wako) and cultured in RPMI 1640 medium supplemented with 1 ng/ml recombinant human interleukin-2 (rhIL-2, R&D Systems).
2.5. Characterization of rhesus macaque DC
The morphological changes of DC were examined under ordinary light microscope, phase contrast microscope and scanning electron microscope. The phenotype of the rhesus monkey peripheral blood monocyte-derived dendritic cells in vitro was analyzed by flow cytometry (FCM) using the following fluorescence-labeled mouse anti-non-human primate monoclonal antibodies: HLA-DR, DP, DQ-PE(clone Tu39, BD), CD83-PE(clone HB15e, BD), CD86-FITC (clone FUN-1, BD), CD1a-PE(clone BL 6, Beckman Coulter) and PE-conjugated mouse antihuman DC-SIGN monoclonal antibodies, CD209-PE (Clone 120507, R&D Systems), which exhibited the highest affinity to both human DC-SIGN and rhesus macaque DC-SIGN. Cell proliferation effect of auto T cell activated by DC infected with SV40 at a multiplicity of infection (MOI) of 20 in mixed lymphocyte reaction (MLR) were mensurated by 3Hthymidine (3H-TdR) incorporation assay. The control dendritic cells were pulsed with 50 ng/ml inactivated SV40.
2.6. Elispot assay
The interleukin 12 (IL-12) enzyme linked immunospot (ELISPOT) assay was carried out in rhesus macaque peripheral blood monocyte-derived DC-SIGN+ dendritic cells using a commercial kit (U-CyTech biosciences, Monkey ELISPOT kit, UH-CT135-PR2). Infective SV40 and inactivated SV40 were used as specific antigen stimulators of the treatment group and the control group respectively. The spots were counted with an automated reader. The number of IL-12 spot forming cells (SFC) was calculated by subtracting the non-specific SFC in the presence of antigen-unloaded DC.
2.7. Statistical analysis
Differences between groups were analyzed by using the statistical software package SPSS 15.0 for Windows. Statistical significance was set at P < 0.05.
3.1. Morphology of rhesus macaque DC
3.2. Phenotype of antigen-unloaded DC
3.3. Phenotype of Antigen-Treated DC
3.4. Function Analysis of Antigen-Treated DC
Auto-T cells proliferation effect in MLR activated by rhesus macaque DC on day 3, 6, 9 of culture was analyzed with 3H-TdR incorporation assay. The results demonstrated that the proliferation of T cells activated by DC treated with inactivated SV40 was more prominent than that activated by DC treated with infective SV40 (P < 0.05).
3.4. Interleukin 12 Secreting activity of antigen-treated DC
Interleukin 12, which is naturally produced by dendritic cells in response to antigen stimulation, is involved in the differentiation of naive T cells. In order to evaluate the function of DC in response to different antigen stimulation, the relative number of IL-12 secreting DC on day 3, 6, 9 of culture following stimulation with inactivated SV40 and infective SV40 was analyzed by an ELISPOT assay. The results showed that the frequency of IL-12 producing cells of inactivated SV40-treated group was higher than that of infective SV40-treated group (P < 0.05).
Dendritic cells can be divided into at least three distinct subsets, two myeloid lineages and one lymphoid lineage. Langerhans cells and interstitial DC constitute two types of immature myeloid DC in vivo [28, 29, 30]. Langerhans cells can be generated from bone marrow, cord blood, or adult blood CD34+ hema topoietic progenitors cultured with GM-CSF, transforming growth factor (TGF)-β, and tumor necrosis factor (TNF)-α in vitro [31, 32, 33]. DC-SIGN-expressing immature dendritic cells can arise from peripheral blood monocytes by culturing with GM-CSF and IL-4 in vitro. These interstitial DC display striking similarities to dermal DC [34, 35].
Recent studies have demonstrated that several pathogens can manipulate DC functions to facilitate their survival by employing DC-SIGN/CD209 which is expressed by a subset of immature DC. This receptor is associated with receptor-mediated cellular endocytosis and involved in the capture of various patho gens. However, it has been demonstrated that DCSIGN+ immature dendritic cells are related to immunosuppressive inducement of many pathogenic microorganism [5, 6].
Cutaneous dendritic cells mainly comprise epidermal Langerin+ dendritic cells, namely, Langerhans cells (LC) and dermal DC-SIGN+ dendritic cells (DDC), namely, interstitial dendritic cells (IDC) . Although both LC and IDC share equally common bone marrow origin, accumulating evidence suggests that their immunological orchestration function appear different in antiviral immunity [37, 38]. DDC located in mucosal tissues of the genital tract are considered to play a central role in the early steps of HIV transfer from DC to T cells through sexual transmission route . DC-SIGN-expressing immature DC exposed to a small amount of HIV particles can promote more efficient infection of T cells than that by free viruses. DC-SIGN-expressing cells can evidently improve the stability and infectivity of HIV. Research shows that HIV particles captured by DC-SIGN-expressing DC remain infectious after 4 days of culture, whereas cell-free virus rapidly loses its infectivity [5, 40]. Langerin+ DC residing in the epidermal or epithelial cells in the skin and mucosa are the first DC subset to encounter HIV-1 and has generally been thought to mediate the spread of HIV-1 to T cells through the C-type lectin Langerin, similarly to transmission by DC-SIGN on dendritic cells. Instead, recent research suggests that in contrast to DC-SIGN, Langerin on LC can protect against HIV-1 transmission by internalization and degradation of the virus [37, 38].
Measles virus (MV) is a high contagious pathogen which can induce profound immunosuppression, resulting in a high mortality rate. It has been demonstrated that DC play a crucial role in the pathogenesis of MV infection [41, 42]. Various immunosuppression mechanisms of MV infection elicited by DC have been described. Although DC-SIGN is not an entry receptor of MV, yet it functions as an attachment receptor to enhance dendritic cell infection .
This work was supported by the National Mega-projects of Science Research for the 11th Five-Year of China (No.2008ZX10001-006) and the opening foundation of the State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital of Medical College, Zhejiang University (No.2008A06).
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