Rath T, Roderfeld M, Graf J, Roeb E
Zentrum für Innere Medizin, Gastroenterologie, Justus-Liebig-Universität Giessen, 35385 Giessen.
Z Gastroenterol. 2009 Aug;47(8):758-69. doi: 10.1055/s-0028-1109520. Epub 2009 Aug 6.
Matrix Metalloproteinases (MMPs) are a family of Zn (2 +)-dependent endopeptidases that are considered to be the most potent proteases in the turnover of the extracellular matrix (ECM). In addition to their capability for degradating virtually all protein components of the ECM, MMPs regulate a variety of non-matrix substrates such as chemokines, cytokines and growth factors. Therefore MMPs play a central role in a variety of physiological and pathological processes such as angiogenesis, wound healing and inflammatory response including mucosal inflammation associated with inflammatory bowel disease (IBD). Apart from mucosal destruction in IBD, recent studies have identified several new functions of MMPs for the pathophysiology of the healthy and inflamed intestine. This article summarises the main activities of MMPs in IBD with emphasis on their pathophysiological relevance and potential clinical implications based on the expression and regulation patterns of these enzymes.
基质金属蛋白酶(MMPs)是一类依赖锌(2+)的内肽酶,被认为是细胞外基质(ECM)更新过程中最具活性的蛋白酶。除了能够降解ECM的几乎所有蛋白质成分外,MMPs还调节多种非基质底物,如趋化因子、细胞因子和生长因子。因此,MMPs在多种生理和病理过程中发挥核心作用,如血管生成、伤口愈合和炎症反应,包括与炎症性肠病(IBD)相关的黏膜炎症。除了IBD中的黏膜破坏外,最近的研究还发现了MMPs在健康和炎症肠道病理生理学中的几种新功能。本文总结了MMPs在IBD中的主要活性,重点基于这些酶的表达和调控模式,阐述它们的病理生理相关性及潜在临床意义。