Nagase Hideaki, Visse Robert, Murphy Gillian
Department of Matrix Biology, Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College London, 1 Aspenlea Road, London W6 8LH, UK.
Cardiovasc Res. 2006 Feb 15;69(3):562-73. doi: 10.1016/j.cardiores.2005.12.002. Epub 2006 Jan 5.
Matrix metalloproteinases (MMPs), also called matrixins, function in the extracellular environment of cells and degrade both matrix and non-matrix proteins. They play central roles in morphogenesis, wound healing, tissue repair and remodelling in response to injury, e.g. after myocardial infarction, and in progression of diseases such as atheroma, arthritis, cancer and chronic tissue ulcers. They are multi-domain proteins and their activities are regulated by tissue inhibitors of metalloproteinases (TIMPs). This review introduces the members of the MMP family and discusses their domain structure and function, proenyme activation, the mechanism of inhibition by TIMPs and their significance in physiology and pathology.
基质金属蛋白酶(MMPs),也称为基质溶素,在细胞的细胞外环境中发挥作用,可降解基质蛋白和非基质蛋白。它们在形态发生、伤口愈合、组织修复以及对损伤(如心肌梗死后)的重塑过程中发挥核心作用,并且在动脉粥样硬化、关节炎、癌症和慢性组织溃疡等疾病的发展过程中也起作用。它们是多结构域蛋白,其活性受金属蛋白酶组织抑制剂(TIMPs)的调节。本综述介绍了MMP家族的成员,并讨论了它们的结构域结构与功能、酶原激活、TIMPs的抑制机制及其在生理和病理学中的意义。