基质金属蛋白酶-3组织抑制剂,多发性硬化的潜在治疗靶点

A. Ghaemi, K. Hamdi, M. Togha, H. Kazemi, A. Gorji
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引用次数: 1

摘要

基质金属蛋白酶蛋白(MMPs)由一大群内蛋白酶组成,它们可以切割细胞外基质的大部分成分。MMPs的活性是通过操纵天然MMP抑制剂(“金属蛋白酶组织抑制剂”(TIMPs))的水平来调节的。在多发性硬化症(MS)的病理过程中,MMP-2和9(明胶酶)过表达,TIMP和MMP表达的平衡被扰乱,导致明胶酶的局部蛋白水解活性增加,血脑屏障(BBB)和髓鞘碱性蛋白的不受控制的降解。因此,明胶酶是MS进化的主要介质,TIMP已被提出作为MS治疗的新靶点。©2012 Academic Journals Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue Inhibitors of Matrix Metalloproteinase-3, Potential Therapeutic Target against Multiple Sclerosis
The Matrix Metalloproteinase Proteins (MMPs) comprise a large group of endoproteinases that cleave most, if not all, components of the extracellular matrix. The activities of MMPs are modulated by manipulation in the levels of natural MMP inhibitors, the "Tissue Inhibitors of Metallo Proteinases" (TIMPs). In a pathological processes of Multiple Sclerosis (MS), the MMP-2 and 9 (Gelatinase) are over expressed and balance of TIMP and MMP expression is perturbed, leading to locally increased proteolytic activity of Gelatinase and uncontrolled degradation of the Blood Brain Barrier (BBB) and myelin basic protein. Therefore, Gelatinase are the main mediators in the evolution of MS and TIMP has been proposed as a novel therapeutic target for MS therapy. © 2012 Academic Journals Inc.
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