Generation and characterization of JCV permissive hybrid cell lines

Ilker K Sariyer1, Mahmut Safak, Jennifer Gordon

  • 1Department of Neuroscience, Center for Neurovirology, Temple University School of Medicine, 1900 North 12th Street, 015-96, Room 203, Philadelphia, PA 19122, USA.

Insights

Researchers developed a novel hybrid cell line by fusing human astrocytes and glioblastoma cells. This new system efficiently supports JC virus (JCV) replication, aiding in the study of progressive multifocal leukoencephalopathy (PML).

Area of Science:

  • Neurovirology
  • Cell Biology
  • Molecular Virology

Background:

  • JC virus (JCV) causes progressive multifocal leukoencephalopathy (PML), a fatal demyelinating disease.
  • JCV primarily infects oligodendrocytes and astrocytes in the central nervous system.
  • Current laboratory propagation of JCV is restricted to primary human fetal glial cells.

Purpose of the Study:

  • To develop a novel and efficient cell culture system for studying JCV.
  • To facilitate research into JCV host-cell interactions and replication mechanisms.
  • To establish a platform for high-throughput screening of anti-JCV agents.

Main Methods:

  • Fusion of primary human fetal astrocytes with the U-87MG human glioblastoma cell line.
  • Characterization of the resulting hybrid cell line's capacity to support JCV.
  • Assessment of JCV replication and viral DNA synthesis in vitro.

Main Results:

  • A new hybrid cell line was successfully generated.
  • This hybrid cell line efficiently supports JCV expression and viral DNA replication.
  • The cell line maintained JCV replication capacity for up to 16 passages.

Conclusions:

  • The developed hybrid cell line provides a reliable in vitro system for JCV research.
  • This system enables detailed studies of JCV biology, host-cell interactions, and cell-type-specific replication.
  • It offers a valuable tool for discovering and screening antiviral therapies against JCV infections.

Related Concept Videos

Hybridoma Technology01:31

Hybridoma Technology

Hybridoma technology is used for the large-scale production of monoclonal antibodies. Monoclonal antibodies bind to only a single antigenic determinant or epitope. Such antibodies are used in research, diagnostics, and disease therapy. The hybridoma technology established in 1975 by Georges Köhler and Cesar Milstein was awarded the Nobel Prize in Medicine in 1984 for revolutionizing research and therapy.
Hybridoma Selection
Commonly used fusion techniques — electroporation, polyethylene glycol...
Cell Lines01:16

Cell Lines

A cell line is a population of cells grown in vitro that can be subcultured over several generations. Normal cells cease to divide after a certain number of cell divisions, a process known as replicative senescence. This number, called the Hayflick limit, was conceptualized by Leonard Hayflick in 1961 when he observed that fetal cells grown in culture could only divide 40-60 times. This limit is due to the shortening of the telomeres during each round of cell division, preventing cell division...
Transgenic Plants02:50

Transgenic Plants

Recombinant DNA technology called transgenesis is often used to add a foreign gene or remove a detrimental gene from an organism. Such genetically modified organisms are called transgenic organisms.
The first-ever transgenic plant was a tobacco plant developed in 1983 that showed resistance against the tobacco mosaic virus. Since then, many transgenic plants have been developed and commercialized for improving the agricultural, ornamental, and horticultural value of a crop plant. Transgenic...
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
In vitro Mutagenesis01:16

In vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
Differentiation of Common Myeloid Progenitor Cells01:15

Differentiation of Common Myeloid Progenitor Cells

Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...