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Survey of virally mediated permeability changes

The Biochemical Journal
|September 15, 1980
PubMed

Insights

Sendai virus alters cell membrane permeability in various brain and lung cells, indicating potential clinical significance. These viral entry and release-associated changes are not limited to paramyxoviruses.

Area of Science:

  • Virology
  • Cell Biology
  • Pathology

Background:

  • Cell membrane permeability is crucial for cellular function and integrity.
  • Viral infections can disrupt cellular processes, including membrane permeability.
  • Understanding viral interactions with host cells is key to developing antiviral strategies.

Purpose of the Study:

  • To investigate the effects of Sendai virus on cell membrane permeability in different cell types.
  • To determine if other viruses cause similar permeability changes.
  • To explore the clinical significance of virus-induced permeability alterations.

Main Methods:

  • Organotypic cultures of ferret lung and nasal turbinate were exposed to Sendai virus.
  • Primary brain cell cultures (cerebellum, ependymal, forebrain) were treated with Sendai virus.
  • Various cell lines (BHK, Lettrée, MDBK) and human leucocytes were used to assess viral effects on permeability.

Main Results:

  • Sendai virus induced significant permeability changes in brain cells and ferret lung/nasal tissues.
  • Influenza virus, rabies virus, and vesicular-stomatitis virus did not cause comparable permeability changes.
  • Serum from viral hepatitis patients alone did not affect leucocyte permeability, but potentiated Sendai virus-induced changes.
  • MDBK cells infected with Sendai virus exhibited permeability changes during viral release.

Conclusions:

  • Permeability changes are associated with specific paramyxoviruses like Sendai virus during entry and release.
  • These viral-induced permeability alterations are not restricted to a specific cell type.
  • The findings suggest potential clinical significance in various viral infections due to cell permeability disruption.

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