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纤溶酶原受体:第一个四分之一世纪。

Plasminogen receptors: the first quarter century.

机构信息

Department of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Semin Thromb Hemost. 2013 Jun;39(4):329-37. doi: 10.1055/s-0033-1334483. Epub 2013 Mar 26.

Abstract

The interaction of plasminogen with cell surfaces results in promotion of plasmin formation and retention on the cell surface. This results in arming cell surfaces with the broad-spectrum proteolytic activity of plasmin. Over the past quarter century, key functional consequences of the association of plasmin with the cell surface have been elucidated. Physiologic and pathophysiologic processes with plasmin-dependent cell migration as a central feature include inflammation, wound healing, oncogenesis, metastasis, myogenesis, and muscle regeneration. Cell surface plasmin also participates in neurite outgrowth and prohormone processing. Furthermore, plasmin-induced cell signaling also affects the functions of inflammatory cells, via production of cytokines, reactive oxygen species, and other mediators. Finally, plasminogen receptors regulate fibrinolysis. In this review, we highlight emerging data that shed light on longstanding controversies and raise new issues in the field. We focus on (1) the impact of the recent X-ray crystal structures of plasminogen and the development of antibodies that recognize cell-induced conformational changes in plasminogen on our understanding of the interaction of plasminogen with cells; (2) the relationship between apoptosis and plasminogen binding to cells; (3) the current status of our understanding of the molecular identity of plasminogen receptors and the discovery of a structurally unique novel plasminogen receptor, Plg-RKT; (4) the determinants of the interplay between distinct plasminogen receptors and cellular functions; and (5) new insights into the role of colocalization of plasminogen and plasminogen activator receptors on the cell surface.

摘要

纤溶酶原与细胞表面的相互作用导致纤溶酶的形成和在细胞表面的保留得到促进。这使得细胞表面具有纤溶酶的广谱蛋白水解活性。在过去的四分之一个世纪中,纤溶酶与细胞表面结合的关键功能后果已经阐明。以纤溶酶依赖性细胞迁移为中心特征的生理和病理生理过程包括炎症、伤口愈合、肿瘤发生、转移、肌生成和肌肉再生。细胞表面纤溶酶还参与神经突生长和前激素加工。此外,纤溶酶诱导的细胞信号转导还通过产生细胞因子、活性氧和其他介质来影响炎症细胞的功能。最后,纤溶酶原受体调节纤维蛋白溶解。在这篇综述中,我们强调了新出现的数据,这些数据阐明了该领域长期存在的争议,并提出了新的问题。我们重点关注:(1)纤溶酶原的最近 X 射线晶体结构和识别纤溶酶原诱导的细胞构象变化的抗体的发展对我们理解纤溶酶原与细胞相互作用的影响;(2)细胞凋亡与纤溶酶原与细胞结合的关系;(3)目前对纤溶酶原受体的分子身份的理解状况以及发现一种结构独特的新型纤溶酶原受体 Plg-RKT;(4)不同纤溶酶原受体与细胞功能之间相互作用的决定因素;(5)关于纤溶酶原和纤溶酶原激活剂受体在细胞表面共定位的作用的新见解。

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