SIV-induced activation of the blood-brain barrier requires cell-associated virus and is not restricted to endothelial cell activation
: It has never been determined if activation of the blood‐brain barrier (BBB) during simian immunodeficiency virus/human immunodeficiency virus (SIV/HIV) infection is a function of high levels of circulating virus or if the virus has to be within a cell capable of crossing the BBB to activate it. I...
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Published in: | Journal of medical primatology Vol. 33; no. 5-6; pp. 236 - 242 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford, UK
Munksgaard International Publishers
01-10-2004
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Subjects: | |
Online Access: | Get full text |
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Summary: | : It has never been determined if activation of the blood‐brain barrier (BBB) during simian immunodeficiency virus/human immunodeficiency virus (SIV/HIV) infection is a function of high levels of circulating virus or if the virus has to be within a cell capable of crossing the BBB to activate it. In vitro models of the BBB are becoming recognized as an acceptable method for determining the cellular events associated with HIV neuroinvasion. Cell free virus (when added in the physiologically relevant lumen) although capable of activating the endothelial cells of our in vitro BBB did not activate astrocytes beneath. SIVmac251‐infected CEMx174 cells, however, were capable of activating both components of the BBB model. Here we demonstrate that an in vitro model of the BBB can be activated in a physiologically relevant manner, that SIV requires to be cell‐associated and that endothelial cells of the BBB are not the only components that are activated during SIV neuroinvasion. |
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Bibliography: | istex:52E0E8872782FEC515AEB18CE7374F55272EF347 ark:/67375/WNG-NT0QVNXJ-S ArticleID:JMP077 Funding: This work was supported by public health service grants NS30769, MH61192, AA13828 and RR00164. A. Lackner is the recipient of an Elizabeth Glaser Scientist Award. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0047-2565 1600-0684 |
DOI: | 10.1111/j.1600-0684.2004.00077.x |