Matrix metalloproteinase expression in an experimentally-induced DTH model of multiple sclerosis in the rat CNS

被引:144
作者
Anthony, DC
Miller, KM
Fearn, S
Townsend, MJ
Opdenakker, G
Wells, GMA
Clements, JM
Chandler, S
Gearing, AJH
Perry, VH
机构
[1] Univ Oxford, Dept Pharmacol, CNS Inflammat Grp, Oxford OX1 3QT, England
[2] British Biotechnol Pharmaceut, Oxford OX4 5LY, England
[3] Katholieke Univ Leuven, Rega Inst, B-3000 Louvain, Belgium
关键词
matrix metalloproteinase; multiple sclerosis; delayed-type hypersensitivity;
D O I
10.1016/S0165-5728(98)00046-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In an experimentally-induced DTH model of MS, we examined mRNA and protein expression of a range of MMPs and of TNF alpha to establish the contribution that individual MMPs might make to the pathogenesis. In control rat brain, mRNA for all of the MMPs examined was detectable. However, by immunohistochemistry, only MMP-2 could be detected. In the DTH lesions, significant increases in the level of mRNA expression were observed for MMP-7, MMP-8, MMP-12, and TNF alpha. Where expression of MMP mRNA was increased, there was a corresponding increase in protein expression detected by immunohistochemistry. To determine whether the upregulated MMPs could invoke destructive events in the CNS, highly purified activated MMP-7, MMP-8, and MMP-9 were stereotaxically injected into the brain parenchyma. All provoked recruitment of leukocytes and BBB breakdown. In addition, MMPs 7 and 9 induced loss of myelin staining. In conclusion, specific MMPs are upregulated in DTH lesions; for the most part, measurement of mRNA was a predictor of increased protein expression. From our injections of MMPs, it is clear that the upregulated MMPs in the DTH lesions could participate in the disruption of the BBB, leukocyte recruitment, and tissue damage. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:62 / 72
页数:11
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