G蛋白偶联受体(GPCR)介导的Ras适应性和趋化性填补空白。

Q2 Biochemistry, Genetics and Molecular Biology
Small GTPases Pub Date : 2020-09-01 Epub Date: 2018-05-29 DOI:10.1080/21541248.2018.1473671
Xuehua Xu
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引用次数: 5

摘要

真核细胞通过G蛋白偶联受体(GPCR)信号通路感知和迁移到化学引诱剂梯度。趋化性的迷人特征是细胞通过“适应”在具有巨大浓度范围的趋化剂梯度中迁移。适应性细胞不再对当前的刺激作出反应,但对更强的刺激仍保持敏感,这为在大范围浓度梯度下趋化提供了基本策略。Ras激活是gpcr介导的化学感应信号通路显示适应性的第一步。然而,Ras适应的分子机制尚不完全清楚。在这里,我们强调了C2GAP1,一个gpcr激活的Ras负调节因子,局部抑制Ras信号以适应和远距离趋化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Filling GAPs in G protein- coupled receptor (GPCR)-mediated Ras adaptation and chemotaxis.

Eukaryotic cells sense and migrate toward chemoattractant gradients using G protein-coupled receptor (GPCR) signaling pathways. The fascinating feature of chemotaxis is that cells migrate through chemoattractant gradients with huge concentration ranges by "adaptation." Adaptive cells no longer respond to the present stimulus but remain sensitive to stronger stimuli, providing the fundamental strategy for chemotaxis through gradients with a broad range of concentrations. Ras activation is the first step in the GPCR-mediated chemosensing signaling pathways that displays adaptation. However, the molecular mechanism of Ras adaptation is not fully understood. Here, we highlight C2GAP1, a GPCR-activated Ras negative regulator, that locally inhibits Ras signaling for adaptation and long-range chemotaxis in D. discoideum.

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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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