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1型纤溶酶原激活物抑制剂、细胞外基质与玻连蛋白之间的相互作用

Interactions between type 1 plasminogen activator inhibitor, extracellular matrix and vitronectin.

作者信息

Seiffert D, Mimuro J, Schleef R R, Loskutoff D J

机构信息

Committee on Vascular Biology, Research Institute of Scripps Clinic, La Jolla, CA 92037.

出版信息

Cell Differ Dev. 1990 Dec 2;32(3):287-92. doi: 10.1016/0922-3371(90)90041-t.

Abstract

Regulation of plasminogen activation is a key process in controlling proteolytic events in the extracellular matrix (ECM) and this regulation is achieved through the action of specific plasminogen activator (PA) inhibitors (PAIs). Type I PAI (PAI-1) is the physiological inhibitor both of urinary-type PA (u-PA) and tissue-type PA (t-PA) (Loskutoff et al., 1989) and is a major component of the ECM of cultured cells. This inhibitor may protect ECM constituents against cellular proteases and thus influence the cell migration and tissue destruction that occurs during development, inflammation and tumor metastasis. In this review, we discuss the properties of PAI-1 and the evidence that the binding of PAI-1 to ECM is mediated by serum-derived vitronectin (Vn).

摘要

纤溶酶原激活的调节是控制细胞外基质(ECM)中蛋白水解事件的关键过程,这种调节是通过特异性纤溶酶原激活剂(PA)抑制剂(PAIs)的作用来实现的。I型PAI(PAI-1)是尿激酶型PA(u-PA)和组织型PA(t-PA)的生理性抑制剂(Loskutoff等人,1989年),并且是培养细胞ECM的主要成分。这种抑制剂可能保护ECM成分免受细胞蛋白酶的影响,从而影响在发育、炎症和肿瘤转移过程中发生的细胞迁移和组织破坏。在这篇综述中,我们讨论了PAI-1的特性以及PAI-1与ECM结合由血清来源的玻连蛋白(Vn)介导的证据。

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