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Published on: May 12, 2014
Growth of JC virus in adult human brain cell cultures
Abstract:
Adult human brain (AHB) cells infected with JC virus (JCV) developed a cytopathic effect (CPE) beginning 12--14 days after infection. Ultrastructurally, 37--40 nm papova virions were seen in the nuclei of infected cells, and both T and V antigen were demonstrated by indirect immunofluorescence. The hemagglutinating titer of JCV in infected AHB cells was 10--40 times higher than the amount of JCV used to initiate infection. AHB cells are more readily available than primary human fetal brain cells, they can be subcultured 15--25 times in vitro and they support JCV replication after multiple subcultivations. These properties make the AHB cell line useful for propagating JCV.
Insights
Adult human brain cells infected with JC virus (JCV) support viral replication and show cytopathic effects. This makes the AHB cell line a valuable tool for JCV propagation.
Area of Science:
- Virology
- Cell Biology
- Neuroscience
Background:
- JC virus (JCV) is a human polyomavirus.
- JCV infection can cause progressive multifocal leukoencephalopathy (PML).
- Understanding JCV replication is crucial for developing antiviral strategies.
Purpose of the Study:
- To investigate the susceptibility of adult human brain (AHB) cells to JC virus (JCV) infection.
- To evaluate the utility of AHB cells for JCV propagation in vitro.
- To characterize the cytopathic effects and viral antigen expression in JCV-infected AHB cells.
Main Methods:
- Infection of AHB cells with JCV.
- Observation of cytopathic effects (CPE) over time.
- Ultrastructural analysis to identify papova virions.
- Indirect immunofluorescence to detect T and V antigens.
- Hemagglutination assays to quantify viral titers.
Main Results:
- JCV infection induced cytopathic effects in AHB cells starting at 12-14 days post-infection.
- Papova virions were observed in the nuclei of infected cells.
- T and V antigens were detected, confirming viral replication.
- JCV hemagglutinating titers increased 10-40 fold in infected AHB cells.
- AHB cells supported JCV replication even after multiple subcultivations.
Conclusions:
- Adult human brain cells are susceptible to JC virus infection and support viral replication.
- The AHB cell line is a practical and effective model for propagating JC virus in vitro.
- AHB cells offer advantages over primary human fetal brain cells due to availability and subcultivation potential.
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