Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tuebingen, Tuebingen, Germany.
DFG Cluster of Excellence 2180 'Image-guided and Functional Instructed Tumor Therapy' (IFIT), University of Tuebingen, Tubingen, Germany.
Front Immunol. 2020 Feb 5;11:44. doi: 10.3389/fimmu.2020.00044. eCollection 2020.
Platelets have a crucial function in maintaining hemostasis. However, beyond their role in coagulation and thrombus formation, platelets have been implicated to affect various pathophysiological conditions such as infectious diseases, autoimmune disorders, and cancer. It is well-established that platelets aid local cancer growth by providing growth factors or contributing to cancer angiogenesis. In addition, they promote metastasis, among others by facilitation of tumor cell-extravasation and epithelial-to-mesenchymal-like transition as well as protecting metastasizing cancer cells from immunosurveillance. A variety of membrane-bound and soluble platelet-derived factors are involved in these processes, and many aspects of platelet biology in both health and disease are regulated by platelet-associated metalloproteinases and their inhibitors. Platelets synthesize (i) members of the matrix metalloproteinase (MMP) family and also inhibitors of MMPs such as members of the "tissue inhibitor of metalloproteinases" (TIMP) family as well as (ii) members of the "a disintegrin and metalloproteinase" (ADAM) family including ADAM10. Notably, platelet-associated metalloproteinase activity not only influences functions of platelets themselves: platelets can also induce expression and/or release of metalloproteinases e.g., in leukocytes or cancer cells, and ADAMs are emerging as important components by which platelets directly affect other cell types and function. This review outlines the function of metalloproteinases in platelet biology with a focus on ADAM10 and discusses the role of platelet-derived metalloproteinases in the interaction of platelets with components of the immune system and/or cancer cells.
血小板在维持止血方面具有至关重要的功能。然而,除了在凝血和血栓形成中的作用外,血小板还被认为会影响各种病理生理状况,如传染病、自身免疫性疾病和癌症。众所周知,血小板通过提供生长因子或促进癌症血管生成来帮助局部癌症生长。此外,它们还促进转移,例如通过促进肿瘤细胞外渗和上皮-间充质转化以及保护转移的癌细胞免受免疫监视。多种膜结合和可溶性血小板衍生因子参与这些过程,并且血小板在健康和疾病中的许多生物学特性都受到血小板相关金属蛋白酶及其抑制剂的调节。血小板合成 (i) 基质金属蛋白酶 (MMP) 家族的成员,以及 MMP 的抑制剂,如“金属蛋白酶组织抑制剂” (TIMP) 家族的成员,以及 (ii)“解整合素和金属蛋白酶” (ADAM) 家族的成员,包括 ADAM10。值得注意的是,血小板相关金属蛋白酶活性不仅会影响血小板自身的功能:血小板还可以诱导白细胞或癌细胞中金属蛋白酶的表达和/或释放,并且 ADAMs 作为血小板直接影响其他细胞类型和功能的重要组成部分而出现。本文综述了金属蛋白酶在血小板生物学中的功能,重点介绍了 ADAM10,并讨论了血小板衍生金属蛋白酶在血小板与免疫系统成分和/或癌细胞相互作用中的作用。