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髓系细胞表达的触发受体-1(TLT-1)的神秘性质。

The enigmatic nature of the triggering receptor expressed in myeloid cells -1 (TLT- 1).

机构信息

, Department of Biology, University of Puerto Rico- Rio Piedras- Molecular Science Research Center, San Juan, Puerto Rico.

出版信息

Platelets. 2021 Aug 18;32(6):753-760. doi: 10.1080/09537104.2021.1881948. Epub 2021 Feb 9.

Abstract

Receptors are important pharmacological targets on cells. The Triggering Receptor Expressed on Myeloid Cells (TREM) - Like Transcript - 1 is an abundant, yet little understood, platelet receptor. It is a single Ig domain containing receptor isolated in the α-granules of resting platelets and brought to the platelet surface upon activation. On platelets, the integrin αIIbβ3 is the major receptor having roughly 80,000 copies. αIIbβ3 is a heterodimeric multidomain structure that mediates platelet aggregation through its interaction with the plasma protein fibrinogen. Anti-platelet drugs have successfully targeted αIIbβ3 to control thrombosis. Like αIIbβ3, TLT-1 also binds fibrinogen, making its role in platelet function somewhat obscure. In this review, we highlight the known structural features of TLT-1 and present the challenges of understanding TLT-1 function. In our analysis of the dynamics of the platelet surface after activation we propose a model in which TLT-1 supports αIIbβ3 function as a mechanoreceptor that may direct platelets toward immune function.

摘要

受体是细胞上重要的药理学靶点。髓样细胞表达的触发受体(TREM)样转录物-1 是一种丰富但知之甚少的血小板受体。它是一种在静止血小板的α-颗粒中分离出来的单免疫球蛋白结构域受体,在激活时被带到血小板表面。在血小板上,整合素 αIIbβ3 是主要的受体,大约有 80000 个拷贝。αIIbβ3 是一种异二聚体多结构域结构,通过与血浆蛋白纤维蛋白原的相互作用介导血小板聚集。抗血小板药物已成功靶向 αIIbβ3 以控制血栓形成。与 αIIbβ3 一样,TLT-1 也与纤维蛋白原结合,使其在血小板功能中的作用有些模糊。在本综述中,我们强调了 TLT-1 的已知结构特征,并提出了理解 TLT-1 功能的挑战。在我们对激活后血小板表面动力学的分析中,我们提出了一个模型,其中 TLT-1 作为机械受体支持 αIIbβ3 功能,这可能使血小板向免疫功能方向发展。

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