Hepatitis B virus infection and replication in human bone marrow mesenchymal stem cells
© Ma et al; licensee BioMed Central Ltd. 2011
Received: 18 September 2011
Accepted: 31 October 2011
Published: 31 October 2011
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© Ma et al; licensee BioMed Central Ltd. 2011
Received: 18 September 2011
Accepted: 31 October 2011
Published: 31 October 2011
Hepatitis B virus (HBV) infection is a blood borne infectious disease that affects the liver. Human bone marrow mesenchymal stem cells (BMSCs) may serve as a cell source for adult stem cell transplantation in liver repair. However, the susceptibility of human BMSCs to HBV infection is poorly understood. The aim of this study was to investigate the infection and replication of HBV in cultures of human BMSCs.
Human BMSCs were confirmed using flow cytometry. Intracellular HBV DNA was detected at d 2 after infection and maintained at relatively high levels from d 6 to d 12. The maximal level of intracellular HBV DNA was 9.37 × 105 copies/mL. The extracellular HBV DNA was observed from d 3 to d 15, and the levels ranged from 3.792 × 102 copies/mL to 4.067 × 105 copies/mL. HBsAg in the culture medium was detected from d 2 to d 16. HBeAg secretion was positive from d 5 to d 13. HBcAg constantly showed positive signals in approximately 7%-20% of BMSCs from 2 days after exposure. Intracellular HBV covalently closed circular DNA (cccDNA) could be detected as early as 2 days postinfection, and strong signals were obtained with increasing time.
HBV can infect and replicate in human BMSCs. Human BMSCs may be a useful tool for investigating HBV life-cycle and the mechanism of initial virus-cell interactions.
Hepatitis B is one of the most common infectious diseases worldwide. It has been estimated that 2 billion people have been infected with hepatitis B virus (HBV). In addition, 360 million people have chronic HBV infection, and 0.6 million people die each year from HBV-related liver disease or hepatocellular carcinoma . Despite the existence of a preventative vaccine, HBV represents a substantial threat to public health . A convenient in vitro assay for HBV natural infectivity is currently unavailable, and the early steps of the viral life cycle are not well understood. Primary human hepatocytes are susceptible to HBV [2, 3]. However, the use of this model is hampered by limited resources and the technical difficulties that are associated with primary hepatocyte cultures. In recent years, liver-related stem cells have attracted intense attention due to their proliferative capabilities and inherent characteristics. Previous studies have shown that human bone marrow mesenchymal stem cells (BMSCs) can differentiate into functional hepatocyte-like cells in vitro [4, 5], and restore liver function in animal models of liver failure [6, 7]. However, the susceptibility of human BMSCs to HBV infection is poorly understood. In the present investigation, we demonstrated for the first time that human BMSCs fully supported the fastidious HBV infection, replication, expression, and secretion. Human BMSCs offers a new opportunity for basic research of the HBV life cycle and the mechanism that mediates the early stages of virus-cell interactions.
Under a protocol that was approved by the Ethics Committee of Shandong University, human bone marrow was aspirated from the iliac crest of healthy donors (18-36 years) with their informed consent. All donors had no serologic evidence of hepatitis or previous HBV infection. The mononuclear cell fraction was separated via centrifugation using a Ficoll-Paque gradient and plated at 1 × 105 cells/cm2 in low-glucose DMEM (Gibco) that was supplemented with 10% FBS (Gibco) and 100 IU/mL penicillin and 100 mg/mL streptomycin. The cells were cultured at 37°C in a humidified atmosphere with 50 mL/L CO2 in air. After 3 days, the nonadherent cell fraction was removed by washing with PBS. Monolayers of attached cells were cultured until they reached 70-90% confluence. The cells were passaged five times prior to further analysis to ensure the removal of contaminating hematopoietic cells.
For cell-surface antigen phenotyping, fifth-passage BMSCs were detached and stained with phycoerythrin (PE)-conjugated monoclonal antibodies against CD45 and fluorescein isothiocyanate (FITC)-labeled antibodies against CD34, CD105 and CD90 and analyzed using flow cytometry with a FACScan (Becton Dickinson, USA). All antibodies were purchased from Becton Dickinson. Isotype control experiments were run in parallel using the same concentration of each antibody.
The HepG2.2.15 cell line, which is a stable human hepatocellular carcinoma cell line that is permanently transfected with HBV-DNA, was obtained from the China Center for Type Culture Collection. HepG2.2.15 cells were cultured with high-glucose DMEM (Gibco) that was supplemented with 10% FBS, 100 IU/mL penicillin, 100 mg/mL streptomycin, and 380 ng/mL G418 in an incubator with 95% humidity and 50 mL/L CO2 at 37°C. HepG2.2.15 cells were used as a positive control.
A serum sample for infection was obtained from a hepatitis B patient who was positive for HBsAg, HBeAg, and HBcAb (HBV core antibody) detection and had a HBV DNA serum load that was 5.4 × 108 copies/mL. The patient had received no antiviral therapy prior to the study and was not infected with HCV or HIV. The sera were stored at -80°C until use.
The fifth generation of BMSCs was seeded in six-well culture dishes. FBS was omitted from the media for 24 h. The cells were incubated with L-DMEM and 10% HBV sera concentration. Following 24 h of exposure, the cells were washed 5 times with PBS to remove the unabsorbed virus. PBS that was used in the sixth wash was collected for detection of HBV DNA using PCR. Thereafter, the cells were cultured with complete media and the start of this incubation was taken as time zero. We used one-well of cells without HBV serum as a negative control.
After infection, aliquots of the BMSCs were harvested using trypsin at various times and their culture supernatants were collected in order. All samples were stored at -80°C. The total DNA was extracted from harvested cells and culture medium according to the method described by Klintschar et al . The HBV PCR fluorescent quantitative detection kit (Piji Biotec, Shenzhen, China) was used according to the manufacturer's protocols.
The HBsAg and HBeAg levels in the media of infected BMSCs were measured using electrochemiluminescence (ECL) with the Elecsys 2010 fully-automated ECL analyzer (Roche).
Infected and control cells were fixed in 40 g/L paraformaldehyde for 20 min at 4°C and permeabilized in Triton X-100 (0.5% in PBS). After blocking in goat serum (1:10 dilution in PBS) for 30 min at 37°C, the cells were incubated overnight at 4°C with a specific mouse monoclonal antibody against HBcAg (1:200 dilution) (Millipore). The secondary antibody was a FITC-tagged goat anti-mouse IgG (1:100 dilution) (SouthernBiotech), which was incubated with the cells at 37°C for 30 min. Finally, the cells were incubated for 10 minutes at room temperature in DAPI (0.5 μg/mL in PBS) and observed using an inverted fluorescence microscope (Olympus, Japan). HepG2.2.15 cells were used as a positive control. BMSCs that were not exposed to HBV were used as a negative control.
Episomal DNAs, including HBV cccDNA were extracted as previously described . Briefly, the cells were lysed in lysis buffer (50 mM Tris hydrochloride, 10 mM EDTA, and 1% sodium dodecyl sulfate). The protein-detergent complexes were precipitated using 2.5 M KCl (0.25volume). The lysates were shaken and centrifuged to remove the insoluble material. The supernatant, which contained viral cccDNA, was used to extract DNA using an equal volume of phenol. Nucleic acids were precipitated using 2 volumes of ethanol. Further purification of cccDNA from contaminating single- and double-stranded DNA was performed using the method of Yang . The purified cccDNA samples were subjected to electrophoresis in 1% agarose, transferred to a nitrocellulose filter, and analyzed by Southern blotting using a DIG-labeled whole HBV DNA probe. The DIG High Prime DNA Labeling and Detection Starter Kit I was purchased from Roche, and the hybridization was performed according to the manufacturer's instructions.
The data of HBV DNA, HBsAg, and HBeAg were expressed as mean ± standard deviation (SD). The results were analyzed using descriptive statistics. The statistical analysis was performed using SPSS 13.0 statistic software (SPSS Inc., USA).
Currently, the hepatoma-derived cell line is a well-established and successful system that has been used for the in vitro study of HBV. However, the viral genome is introduced by integration or transfection rather than infection [12, 13]. Therefore, these cell lines are unsuitable for studying the mechanism of the early stages of virus-cell interactions, including viral attachment, penetration, and uncoating. Primary human hepatocytes allow natural penetration and full viral replication. However, the use of primary human hepatocytes is hampered by limited resources and technical difficulties that are associated with human hepatocyte culture. Treatment of primary hepatocytes with DMSO or PEG can enhance and prolong HBV infection [2, 3], but these chemicals may induce artificial mechanisms for viral entry. Therefore, an ideal cell system for the study of HBV in vitro is needed. In the present study, an HBV-infected human BMSCs culture system was established using the method of co-cultivation of BMSCs with HBV-positive serum in vitro.
Several methods have been used to isolate BMSCs, including plastic adherence, gradient density centrifugation and immunomagnetic selection. The number of MSCs in the bone marrow is small. There are approximately 2 to 5 cells that are present in every 1 × 106 mononuclear cells . The cells that are selected from the human bone marrow mononuclear cell fraction by plastic adherence display typical features of BMSCs . Therefore, we combined the gradient density centrifugation with plastic adherence to isolate human BMSCs and to obtain abundant and pure BMSCs. In addition, flow cytometric analysis further confirmed human BMSCs identity.
In the present study, initial evaluation of the infection system was performed using quantitative fluorescence PCR (FQ-PCR) for HBV DNA. Previous studies of bone marrow cells have provided insufficient information about the quantitative analysis of HBV-DNA in culture supernatants and infected cells. FQ-PCR is highly sensitive and permits the use of small amounts of material. The FQ-PCR method that was used in this study could detect as few as 102 HBV genomes per assay. In our experiment, the levels of the intracellular and extracellular HBV-DNA were assayed during the culture period. No HBV-DNA was detected in the cells or media at time zero. Therefore, these DNA molecules could not be carryovers of the infecting virions. Viral DNA in the medium was not detected until 3 days after infection. Therefore, the appearance of HBV DNA in the medium of infected BMSCs was the result of de novo viral gene product synthesis. In contrast, no HBV-DNA was detected in uninfected BMSCs. These date indicate that HBV could infect the cultured human BMSCs and replicate in them in vitro.
In addition to assay of HBV DNA, secretory HBV antigens were identified using ECL. HBsAg represents a multi-functional activity that plays a critical role in the binding of HBV and target cells . The expression of HBeAg is closely linked to HBV DNA replication . Therefore, our detection of the two HBV-specific antigens provided evidence that replication and expression of the HBV genome occurred in infected BMSCs. Moreover, the efficiency of HBV infection of BMSCs in vitro, based on the expression of the HBcAg, was comparable with the infection of primary human hepatocytes  and human hepatoma cell lines [12, 17]. HBcAg forms the capsid of viral particles and is essential for viral genome DNA replication. Our results suggest that HBV can replicate actively in cultured human BMSCs.
In order to provide further supporting evidence that HBV can infect and replicate in human BMSCs, we analyzed the intracellular HBV cccDNA via Southern blot hybridization. In our experiment, intracellular cccDNA was detected in infected BMSCs as early as 2 days postinfection. This phenomenon is consistent with the view that the appearance of cccDNA in the nucleus is one of the earliest events in the replication of hepadnaviruses . The cccDNA is thought to be the template for transcription of mRNAs and pregenome RNA, which for synthesis of new DNA genomes via reverse transcription . Therefore, our experimental infection system not only surports HBV infection but also reproduces the complete cycle of viral replication. Nevertheless, Southern blot analysis of total DNA isolated from BMSCs failed to demonstrate the presence of the relaxed circular and single stranded forms of HBV DNA (data not shown). This was not surprising due to the relatively low titer of HBV DNA (102-105 copies/mL) as measured in the infected BMSCs using FQ-PCR. Similar results in primary human hepatocytes in vitro have been reported previously . This may be due to a different host environment in culture compared to hepatocytes in vivo.
In our study, we also performed reinfection experiments. The progeny virions were infectious (data not shown). The media of infected BMSCs were incubated with mouse antibodies directed against HBsAg (anti-HBsAg). The media were assayed for infectivity using FQ-PCR and ECL. The anti-HBsAg antibodies reduced the infectivity (data not shown). These results suggest that uptake of HBV into BMSCs follows the authentic entry pathway and infected BMSCs can synthesize and secrete infectious virions into the media.
In our experiment, the infected BMSCs were sustained for 10 weeks or more and maintained their characteristic phenotype. As a subset of bone marrow stem cells, BMSCs are relatively easily separated and grown in culture. Due to their excellent proliferation capabilities without losing their initial characteristics, they can overcome the limitations associated with human hepatocyte culture (e.g., scarce resources and technical difficulties). Previous studies have indicated that human BMSCs are capable of differentiating into functional hepatocyte-like cells in vitro [4, 5]. In our studies, we found that HBV could also infect and replicate in the hepatocyte-like cells induced from human BMSCs (data not shown). Interestingly, hepatocyte-like cells from human BMSCs were hard to maintain in cultures and had poor proliferative potential in vitro. These features are similar to adult human hepatocytes. The results of our study demonstrate that human BMSCs display a better advantage over BMSC-derived hepatocyte-like cells in studies of HBV.
It was reported that HBV could infect and replicate in bone marrow cells in vivo . As a subset of bone marrow cells, it remains to be seen whether BMSCs are permissive for productive HBV replication in vivo. In addition, it remains unclear if HBV uses the same pathway/mechanism to infect BMSCs and hepatocytes. These need to investigate in future studies.
In conclusion, several lines of evidence indicate that the human BMSCs can maintain HBV infection in vitro and support the replication of HBV DNA. Our experimental in vitro infection system will be a powerful tool to analyze the complex interactions between HBV and its host cell at the molecular levels and to evaluate different antiviral strategies. Furthermore, our findings with this system provide evidence that HBV exhibits a wider host range than previously reported, and may help explain HBV reinfection in recipients of liver transplants.
Hepatitis B virus
Bone marrow mesenchymal stem cells
covalently closed circular DNA
Quantitative fluorescence PCR.
This study was supported by grants from the National Natural Science Foundation of China (NSFC No.81071340) and the Natural Science Foundation of Shandong Province (No. Y2008C68).
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.