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一条通过ELMO/DOCK复合物从G蛋白偶联受体(GPCR)信号传导至Rac介导的肌动蛋白细胞骨架的捷径。

A shortcut from GPCR signaling to Rac-mediated actin cytoskeleton through an ELMO/DOCK complex.

作者信息

Xu Xuehua, Jin Tian

机构信息

Chemotaxis Signal Section, Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.

出版信息

Small GTPases. 2012 Jul-Sep;3(3):183-5. doi: 10.4161/sgtp.20271. Epub 2012 May 31.

Abstract

Chemotaxis, chemoattractant-guided directional cell migration, plays major roles in human innate immunity and in development of a model organism Dictyostelium discoideum. Human leukocytes and D. disscoideum share remarkable similarities in the molecular mechanisms that control chemotaxis. These cells use G-Protein-Coupled Receptors (GPCRs), such as chemokine receptors, to control a signaling network that carries out chemotactic gradient sensing and directs cell migration. Diverse chemokines bind to their receptors to activate small G protein Rac through an evolutionarily conserved mechanism. Elmo and Dock180 proteins form ELMO/Dock180 complexes functioning as guanine nucleotide exchange factors (GEFs) for Rac activation. However, the linkage between GPCR to Elmo/Dock180 for Rac activation that controls F-actin dynamics remained unclear. Recently, we discovered a novel function of an ELMO protein in Dictyostelium discoideum linking GPCR signaling from Gβ to actin dynamics through regulating Rac activation during chemotaxis.

摘要

趋化作用,即由化学引诱剂引导的定向细胞迁移,在人类先天免疫以及模式生物盘基网柄菌的发育过程中发挥着重要作用。人类白细胞和盘基网柄菌在控制趋化作用的分子机制上具有显著的相似性。这些细胞利用G蛋白偶联受体(GPCRs),如趋化因子受体,来控制一个执行趋化梯度感知并指导细胞迁移的信号网络。多种趋化因子通过一种进化上保守的机制与其受体结合,从而激活小G蛋白Rac。Elmo和Dock180蛋白形成ELMO/Dock180复合物,作为Rac激活的鸟嘌呤核苷酸交换因子(GEFs)发挥作用。然而,在控制F-肌动蛋白动力学的Rac激活过程中,GPCR与Elmo/Dock180之间的联系仍不清楚。最近,我们发现了盘基网柄菌中一种ELMO蛋白的新功能,即在趋化作用过程中,通过调节Rac激活,将GPCR信号从Gβ连接到肌动蛋白动力学。

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Dock180-ELMO cooperation in Rac activation.Dock180与ELMO在Rac激活中的协同作用。
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本文引用的文献

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Chemotaxis, chemokine receptors and human disease.趋化作用、趋化因子受体与人类疾病。
Cytokine. 2008 Oct;44(1):1-8. doi: 10.1016/j.cyto.2008.06.017. Epub 2008 Aug 21.

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