Replication of JC Virus DNA in the G144 Oligodendrocyte Cell Line Is Dependent Upon Akt
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Published on: July 13, 2019
Jesse N Peterson1, Brian Lin1, Jong Shin2
1Department of Developmental, Molecular and Chemical Biology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Abstract:
Progressive multifocal leukoencephalopathy (PML) is an often-fatal demyelinating disease of the central nervous system. PML results when oligodendrocytes within immunocompromised individuals are infected with the human JC virus (JCV). We have identified an oligodendrocyte precursor cell line, termed G144, that supports robust levels of JCV DNA replication, a central part of the JCV life cycle. In addition, we have determined that JC virus readily infects G144 cells. Furthermore, we have determined that JCV DNA replication in G144 cells is stimulated by myristoylated (i.e., constitutively active) Akt and reduced by the Akt-specific inhibitor MK2206. Thus, this oligodendrocyte-based model system will be useful for a number of purposes, such as studies of JCV infection, establishing key pathways needed for the regulation of JCV DNA replication, and identifying inhibitors of this process.IMPORTANCE The disease progressive multifocal leukoencephalopathy (PML) is caused by the infection of particular brain cells, termed oligodendrocytes, by the JC virus. Studies of PML, however, have been hampered by the lack of an immortalized human cell line derived from oligodendrocytes. Here, we report that the G144 oligodendrocyte cell line supports both infection by JC virus and robust levels of JCV DNA replication. Moreover, we have established that the Akt pathway regulates JCV DNA replication and that JCV DNA replication can be inhibited by MK2206, a compound that is specific for Akt. These and related findings suggest that we have established a powerful oligodendrocyte-based model system for studies of JCV-dependent PML.
Insights
A new G144 oligodendrocyte cell line supports JC virus (JCV) infection and DNA replication, crucial for studying progressive multifocal leukoencephalopathy (PML). The Akt pathway regulates JCV replication, offering potential therapeutic targets for PML.
Area of Science:
- Neurovirology
- Cell Biology
- Demyelinating Diseases
Background:
- Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease caused by JC virus (JCV) infection of oligodendrocytes.
- Research into PML pathogenesis is limited by the lack of suitable in vitro models using human oligodendrocytes.
Purpose of the Study:
- To establish and characterize an immortalized human oligodendrocyte precursor cell line (G144) for studying JCV infection and replication.
- To investigate the role of the Akt signaling pathway in regulating JCV DNA replication.
Main Methods:
- Establishment and characterization of the G144 oligodendrocyte precursor cell line.
- Infection of G144 cells with JCV and assessment of viral DNA replication.
- Pharmacological modulation of the Akt pathway using a specific inhibitor (MK2206) and a constitutively active form of Akt.
Main Results:
- The G144 cell line supports robust JCV DNA replication and is readily infected by JCV.
- Constitutively active Akt enhances JCV DNA replication in G144 cells.
- The Akt-specific inhibitor MK2206 significantly reduces JCV DNA replication.
Conclusions:
- The G144 cell line provides a valuable in vitro model for studying JCV infection and replication in oligodendrocytes.
- The Akt pathway is a key regulator of JCV DNA replication, representing a potential therapeutic target for PML.
- This model system facilitates research into JCV-dependent PML and the development of novel antiviral strategies.
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