Skip to main content
Log in

Japanese encephalitis virus is transported across the cerebral blood vessels by endocytosis in mouse brain

  • REGULAR ARTICLE
  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract 

Japanese encephalitis (JE) virus principally infects neuron systems of animals and causes severe encephalitis. The mechanism by which the virus enters the central nervous system (CNS) from the circulatory system remains elusive. In this study, electron-microscopic techniques have been used to determine these sequential events in the suckling mouse brain. The results indicate that (1) endocytosis is employed when JE virus is transported across the cerebral blood vessels (CBV) and breaches the blood-brain barrier (BBB). (2) Uncoated vesicles, which may be caveolae, and coated vesicles are involved in the endocytic and transcytotic vesicles of capillary endothelium and pericytes. (3) The JE virus is transported in endocytic vesicles across the endothelial cells and pericytes. (4) Endocytosis and transportation of JE virus in pericytes seems to be the same as that in endothelial cells. (5) The interaction of the viral envelope and cell membrane of endothelial cells and pericytes plays an important role in the endocytosis. This study elucidates the infectious processes of JE virus entering the CNS from the circulatory system in the mouse brain.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 9 September 1997 / Accepted: 22 April 1998

Rights and permissions

Reprints and permissions

About this article

Cite this article

Liou, ML., Hsu, CY. Japanese encephalitis virus is transported across the cerebral blood vessels by endocytosis in mouse brain. Cell Tissue Res 293, 389–394 (1998). https://doi.org/10.1007/s004410051130

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s004410051130

Navigation