Distinct roles for matrix metalloproteinase-2 and α4 integrin in autoimmune T cell extravasation and residency in brain parenchyma during experimental autoimmune encephalomyelitis

被引:74
|
作者
Graesser, D [1 ]
Mahooti, S [1 ]
Madri, JA [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
关键词
metalloproteinases; experimental autoimmune encephalomyelitis; integrins; VLA-4; T lymphocytes;
D O I
10.1016/S0165-5728(00)00275-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expression of alpha 4 integrin by auto-reactive T cells is critical for their ability to induce EAE, an autoimmune disease of the central nervous system in mice, used as a model to study human multiple sclerosis. Having previously identified one role for alpha 4 integrin in adhesion-mediated induction of matrix metalloproteinase-2 (MMP-2), an enzyme that degrades the subendothelial basement membrane matrix, we investigated independent roles for MMP-2 and alpha 4 integrin during EAE. The data suggest that expression of alpha 4 integrin by auto-reactive T cells is important not only in mediating MMP-2 induction to facilitate entry into the CNS, but also plays a role in maintaining residency within the CNS. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:121 / 131
页数:11
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