Differential expression of ADAMTS-1,-4,-5 and TIMP-3 in rat spinal cord at different stages of acute experimental autoimmune encephalomyelitis

被引:23
作者
Cross, AK
Haddock, G
Surr, J
Plumb, J
Bunning, RAD
Buttle, DJ
Woodroofe, MN
机构
[1] Sheffield Hallam Univ, Sch Sci & Math, Div Biomed Sci, Ctr Biomed Res,Dept Hlth & Wellbeing, Sheffield S1 1WB, S Yorkshire, England
[2] Univ Sheffield, Sch Med, Div Genom Med, Sheffield S10 2RX, S Yorkshire, England
基金
英国惠康基金;
关键词
ADAMTS; EAE; extracellular matrix; inflammation; brain;
D O I
10.1016/j.jaut.2005.09.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Experimental autoitrumme encephalomyelitis (EAE) is an animal model of inflammatory demyelination, a pathological event common to multiple sclerosis (MS). During CNS inflammation there are alterations in the extracellular matrix (ECM). A Disintegrin and Metalloproteinase with 7-brombospondin motifs (ADAMTS)-1, -4 and -5 are proteases present in the CNS, which are able to cleave the aggregating chondroitin sulphate proteoglycans, aggrecan, phosphacan, neurocan and brevican. It is therefore important to investigate changes in their expression in different stages of EAE induction. We have investigated expression of ADAMTS-I, -4, -5 and tissue inhibitor of metalloproteinase (TIMP)-3, by real-time RT-PCR. We have also examined protein expression of ADAMTS-1, -4 and -5 by western blotting and immunocytochemistry in spinal cord from animals at different stages of disease progression. Our study demonstrated a decrease in ADAMTS-4 mRNA and protein expression. TIMP-3 was decreased at the mRNA level although protein levels were increased in diseased animals compared to controls. Our study identifies changes in ADAMTS expression during the course of CNS inflammation which may contribute to ECM degradation and disease progression. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
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