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ADAMTS-1、-4、-5及TIMP-3在正常及多发性硬化中枢神经系统白质中的表达

Expression of ADAMTS-1, -4, -5 and TIMP-3 in normal and multiple sclerosis CNS white matter.

作者信息

Haddock G, Cross A K, Plumb J, Surr J, Buttle D J, Bunning R A D, Woodroofe M N

机构信息

Biomedical Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.

出版信息

Mult Scler. 2006 Aug;12(4):386-96. doi: 10.1191/135248506ms1300oa.

Abstract

ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) -1, -4 and -5 proteases have been identified in the CNS at the mRNA level. These glutamyl endopeptidases, inhibited by tissue inhibitor of metalloproteinases (TIMP)-3, are key enzymes in the degradation of the aggregating chondroitin sulphate proteoglycans (CSPGs), and may therefore play a role in CNS extracellular matrix (ECM) changes in multiple sclerosis (MS). We have investigated ADAMTS and TIMP-3 expression in normal and MS CNS white matter by real-time RT-PCR, western blotting and immunohistochemistry. We report for the first time the presence of ADAMTS-1, -4 and -5 in normal and MS white matter. Levels of ADAMTS-1 and -5 mRNA were decreased in MS compared to normal tissue, with no significant change in ADAMTS-4 mRNA levels. Protein levels of ADAMTS-4 were significantly higher in MS tissue compared to normal tissue. Immunohistochemical studies demonstrated that ADAMTS-4 was associated predominantly with astrocytes with increased expression within MS lesions. TIMP-3 mRNA was significantly decreased in MS compared to controls. These studies suggest a role for ADAMTS-4 in the pathogenesis of MS. Further studies on the activity of ADAMTS-4 will enable a better understanding of its role in the turnover of the ECM of white matter in MS.

摘要

含血小板反应蛋白基序的解聚素样金属蛋白酶(ADAMTS)-1、-4和-5蛋白酶已在中枢神经系统(CNS)中通过mRNA水平得以鉴定。这些谷氨酰内肽酶受金属蛋白酶组织抑制剂(TIMP)-3抑制,是聚集性硫酸软骨素蛋白聚糖(CSPG)降解中的关键酶,因此可能在多发性硬化症(MS)的中枢神经系统细胞外基质(ECM)变化中发挥作用。我们通过实时逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法和免疫组织化学研究了正常和MS中枢神经系统白质中ADAMTS和TIMP-3的表达情况。我们首次报道了正常和MS白质中存在ADAMTS-1、-4和-5。与正常组织相比,MS中ADAMTS-1和-5的mRNA水平降低,而ADAMTS-4的mRNA水平无显著变化。与正常组织相比。MS组织中ADAMTS-4的蛋白质水平显著更高。免疫组织化学研究表明,ADAMTS-4主要与星形胶质细胞相关,在MS病变中表达增加。与对照组相比,MS中TIMP-3的mRNA显著降低。这些研究提示ADAMTS-4在MS发病机制中发挥作用。对ADAMTS-4活性的进一步研究将有助于更好地理解其在MS白质ECM周转中的作用。

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