Ludwig Thomas
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven Connecticut 06520-8026, USA.
Bioessays. 2005 Nov;27(11):1181-91. doi: 10.1002/bies.20306.
Proteolytic cleavage of extracellular matrix (ECM) is a critical regulator of many physiological and pathological events. It affects fundamental processes such as cell growth, differentiation, apoptosis and migration. Most proteases are produced as inactive proenzymes that undergo proteolytic cleavage for activation. Proteolytic activity is additionally modified by endogenous inhibitors. Mechanisms that localize and concentrate protease activity in the pericellular microenvironment of cells are prerequisites for processes like angiogenesis, bone development, inflammation and tumor cell invasion. Methods that enable real-time, high-resolution imaging and precise quantification of local proteolytic activity in vitro and in vivo remain major challenges. These methods will play an important role in the understanding of basic principles e.g. in cancer cell invasion, the identification of new therapeutical targets and hence drug design. This review highlights mechanisms and functions of local proteolytic activity with special emphasis on tumor cell invasion and metastasis, and focuses on techniques for the investigation of this process.
细胞外基质(ECM)的蛋白水解切割是许多生理和病理过程的关键调节因子。它影响细胞生长、分化、凋亡和迁移等基本过程。大多数蛋白酶以无活性的酶原形式产生,需经过蛋白水解切割才能激活。蛋白水解活性还会受到内源性抑制剂的修饰。将蛋白酶活性定位并集中在细胞周围微环境中的机制是血管生成、骨骼发育、炎症和肿瘤细胞侵袭等过程的先决条件。能够在体外和体内对局部蛋白水解活性进行实时、高分辨率成像和精确量化的方法仍然是重大挑战。这些方法将在理解例如癌细胞侵袭的基本原理、识别新的治疗靶点以及药物设计等方面发挥重要作用。本综述重点介绍局部蛋白水解活性的机制和功能,特别强调肿瘤细胞侵袭和转移,并着重探讨研究这一过程的技术。