UP-REGULATION AND COEXPRESSION OF ADHESION MOLECULES CORRELATE WITH RELAPSING AUTOIMMUNE DEMYELINATION IN THE CENTRAL-NERVOUS-SYSTEM

被引:157
作者
CANNELLA, B
CROSS, AH
RAINE, CS
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED,ROSE F KENNEDY CTR RES MENTAL RETARDAT & HUMAN DEV,BRONX,NY 10461
[2] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT NEUROSCI,BRONX,NY 10461
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT NEUROL,BRONX,NY 10461
关键词
D O I
10.1084/jem.172.5.1521
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of adhesion molecules on central nervous system (CNS) vessels was examined during chronic relapsing experimental autoimmune encephalomyelitis in the SJL mouse. Two molecules associated with cell adhesion were studied: MECA325, a murine lymph node high endothelial venule marker; and MALA2, the murine homologue of intercellular adhesion molecule 1. During initial disease, upregulated coexpression of these two molecules occurred in the CNS. This correlated with inflammatory cell invasion. During remission, expression was downregulated, and each subsequent relapse was accompanied by corresponding upregulation. Thus, up- and downregulation of adhesion molecules in the target organ appeared to form an integral part ofthe inflammatory process in this autoimmune condition and support a role for receptor-mediated inflammatory cell invasion of relevance to the pathogenesis of multiple sclerosis. © 1990, Rockefeller University Press., All rights reserved.
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页码:1521 / 1524
页数:4
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