Myöhänen H, Vaheri A
Haartman Institute, University of Helsinki, P.O. Box 21, 00014, Helsinki, Finland.
Cell Mol Life Sci. 2004 Nov;61(22):2840-58. doi: 10.1007/s00018-004-4230-9.
The main components in plasminogen activation include plasminogen, tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), urokinase plasminogen activator receptor (uPAR), and plasminogen activator inhibitors-1 and -2 (PAI-1, PAI-2). These components are subject to extensive regulation and interactions with for example, pericellular adhesion molecules. Although uPA and tPA are quite similar in structure and have common inhibitors and physiological substrates, their physiological roles are distinct. Traditionally, the role of tPA has been in fibrinolysis and that of uPA in cell migration, especially in cancer cells. Recently several targets for tPA/plasmin have been found in neuronal tissues. The functional role of the PAIs is no longer simply to inhibit overexpressed plasminogen activators, and PAI-2 has an unidentified role in the regulation of cell death.
纤溶酶原激活的主要成分包括纤溶酶原、组织纤溶酶原激活物(tPA)、尿激酶型纤溶酶原激活物(uPA)、尿激酶型纤溶酶原激活物受体(uPAR)以及纤溶酶原激活物抑制剂-1和-2(PAI-1、PAI-2)。这些成分受到广泛调控,并与例如细胞周围黏附分子相互作用。尽管uPA和tPA在结构上非常相似,且具有共同的抑制剂和生理底物,但它们的生理作用却截然不同。传统上,tPA的作用在于纤维蛋白溶解,而uPA的作用在于细胞迁移,尤其是在癌细胞中。最近,在神经组织中发现了tPA/纤溶酶的几个靶点。PAIs的功能作用不再仅仅是抑制过度表达的纤溶酶原激活物,并且PAI-2在细胞死亡调控中具有尚未明确的作用