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Rap1-Interacting Adaptor Molecule (RIAM) 的结构、生化和功能特性。

Structural, biochemical, and functional properties of the Rap1-Interacting Adaptor Molecule (RIAM).

机构信息

Department of Medical Biology, School of Medicine, University of Health Sciences, Istanbul, Turkey.

School of Medicine, Unit of Immunology, Complutense University of Madrid, Madrid, Spain.

出版信息

Biomed J. 2022 Apr;45(2):289-298. doi: 10.1016/j.bj.2021.09.005. Epub 2021 Oct 1.

Abstract

Leukocytes, the leading players of immune system, are involved in innate and adaptive immune responses. Leukocyte adhesion to endothelial cells during transmigration or to antigen presenting cells during T cell activation, requires integrin activation through a process termed inside-out integrin signaling. In hematopoietic cells, Rap1 and its downstream effector RIAM (Rap1-interacting adaptor molecule) form a cornerstone for inside-out integrin activation. The Rap1/RIAM pathway is involved in signal integration for activation, actin remodeling and cytoskeletal reorganization in T cells, as well as in myeloid cell differentiation and function. RIAM is instrumental for phagocytosis, a process requiring particle recognition, cytoskeletal remodeling and membrane protrusion for engulfment and digestion. In the present review, we discuss the structural and molecular properties of RIAM and the recent discoveries regarding the functional role of the Rap1/RIAM module in hematopoietic cells.

摘要

白细胞是免疫系统的主要参与者,参与先天和适应性免疫反应。白细胞在穿越内皮细胞或在 T 细胞激活时与抗原呈递细胞黏附,需要通过称为整合素信号转导的过程激活整合素。在造血细胞中,Rap1 及其下游效应因子 RIAM(Rap1 相互作用衔接分子)构成了整合素激活的基石。Rap1/RIAM 途径参与 T 细胞激活、肌动蛋白重塑和细胞骨架重排的信号整合,以及髓样细胞分化和功能。RIAM 对于吞噬作用至关重要,吞噬作用需要颗粒识别、细胞骨架重塑和膜突起以吞噬和消化。在本综述中,我们讨论了 RIAM 的结构和分子特性以及最近关于 Rap1/RIAM 模块在造血细胞中的功能作用的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b70/9250098/14ae4d2293c9/gr1.jpg

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