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吞噬细胞对磷脂酰丝氨酸的识别:着眼于杀伤作用。

Phosphatidylserine recognition by phagocytes: a view to a kill.

作者信息

Wu Yi, Tibrewal Nitu, Birge Raymond B

机构信息

Department of Biochemistry and Molecular Biology, UMDNJ - New Jersey Medical School, NJ 07103, USA.

出版信息

Trends Cell Biol. 2006 Apr;16(4):189-97. doi: 10.1016/j.tcb.2006.02.003. Epub 2006 Mar 10.

Abstract

The redistribution of phosphatidylserine (PS) to the external surface of the plasma membrane is a key element of apoptotic cell recognition and is a molecular cue that dying cells should be engulfed. Phagocytes interact with PS on apoptotic cells through either the PS receptor or secreted bridging proteins called opsonins. The study of two secreted PS opsonins, MFG-E8 and Gas6 and their receptors alphavbeta5 (and alphavbeta3) integrin and Mer tyrosine kinase, respectively, have provided insights into the temporal and spatial aspects of Rac1 activation following the recognition and internalization of apoptotic cells. Disruption of PS opsonins and their signaling pathways often manifest conditions of inflammation and autoimmune disease. Here, we review recent studies involving PS opsonins, their receptors and their role in the phagocytosis of apoptotic cells.

摘要

磷脂酰丝氨酸(PS)重新分布到质膜外表面是凋亡细胞识别的关键要素,也是一个表明死亡细胞应被吞噬的分子信号。吞噬细胞通过PS受体或称为调理素的分泌型桥接蛋白与凋亡细胞上的PS相互作用。对两种分泌型PS调理素MFG-E8和Gas6及其受体(分别为αvβ5(和αvβ3)整合素和Mer酪氨酸激酶)的研究,为凋亡细胞识别和内化后Rac1激活的时空方面提供了见解。PS调理素及其信号通路的破坏常表现为炎症和自身免疫性疾病状态。在此,我们综述了近期涉及PS调理素、其受体及其在凋亡细胞吞噬作用中作用的研究。

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