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本文引用的文献

1
The role of apical cell-cell junctions and associated cytoskeleton in mechanotransduction.顶端细胞间连接及相关细胞骨架在机械转导中的作用。
Biol Cell. 2017 Apr;109(4):139-161. doi: 10.1111/boc.201600075. Epub 2017 Mar 13.
2
Defining functional interactions during biogenesis of epithelial junctions.定义上皮连接生物发生过程中的功能相互作用。
Nat Commun. 2016 Dec 6;7:13542. doi: 10.1038/ncomms13542.
3
Coronin 1B supports RhoA signaling at cell-cell junctions through Myosin II.冠蛋白1B通过肌球蛋白II在细胞间连接处支持RhoA信号传导。
Cell Cycle. 2016 Nov 16;15(22):3033-3041. doi: 10.1080/15384101.2016.1234549. Epub 2016 Sep 20.
4
The polarity protein Scribble positions DLC3 at adherens junctions to regulate Rho signaling.极性蛋白Scribble将DLC3定位在黏着连接处,以调节Rho信号传导。
J Cell Sci. 2016 Oct 1;129(19):3583-3596. doi: 10.1242/jcs.190074. Epub 2016 Aug 5.
5
Deciphering the Molecular and Functional Basis of RHOGAP Family Proteins: A SYSTEMATIC APPROACH TOWARD SELECTIVE INACTIVATION OF RHO FAMILY PROTEINS.解析RHOGAP家族蛋白的分子与功能基础:一种选择性失活RHO家族蛋白的系统方法
J Biol Chem. 2016 Sep 23;291(39):20353-71. doi: 10.1074/jbc.M116.736967. Epub 2016 Aug 1.
6
Rac1 in human diseases: The therapeutic potential of targeting Rac1 signaling regulatory mechanisms.人类疾病中的Rac1:靶向Rac1信号调节机制的治疗潜力
Small GTPases. 2017 Jul 3;8(3):139-163. doi: 10.1080/21541248.2016.1211398. Epub 2016 Jul 21.
7
Regulating Rho GTPases and their regulators.调节 Rho GTPases 及其调节因子。
Nat Rev Mol Cell Biol. 2016 Aug;17(8):496-510. doi: 10.1038/nrm.2016.67. Epub 2016 Jun 15.
8
Deregulation of Rho GTPases in cancer.癌症中Rho GTP酶的失调。
Small GTPases. 2016 Jul 2;7(3):123-38. doi: 10.1080/21541248.2016.1173767. Epub 2016 Apr 22.
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Interplay between Solo and keratin filaments is crucial for mechanical force-induced stress fiber reinforcement.Solo与角蛋白丝之间的相互作用对于机械力诱导的应力纤维增强至关重要。
Mol Biol Cell. 2016 Mar 15;27(6):954-66. doi: 10.1091/mbc.E15-06-0417. Epub 2016 Jan 28.
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P-cadherin promotes collective cell migration via a Cdc42-mediated increase in mechanical forces.P-钙黏蛋白通过Cdc42介导的机械力增加促进集体细胞迁移。
J Cell Biol. 2016 Jan 18;212(2):199-217. doi: 10.1083/jcb.201505105.

细胞连接处的小 GTP 酶信号传导:构建控制和网络的蛋白质相互作用。

Signaling by Small GTPases at Cell-Cell Junctions: Protein Interactions Building Control and Networks.

机构信息

Molecular Medicine, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London SW7 2AZ, United Kingdom.

出版信息

Cold Spring Harb Perspect Biol. 2018 Oct 1;10(10):a028746. doi: 10.1101/cshperspect.a028746.

DOI:10.1101/cshperspect.a028746
PMID:28893858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6169809/
Abstract

A number of interesting reports highlight the intricate network of signaling proteins that coordinate formation and maintenance of cell-cell contacts. We have much yet to learn about how the in vitro binding data is translated into protein association inside the cells and whether such interaction modulates the signaling properties of the protein. What emerges from recent studies is the importance to carefully consider small GTPase activation in the context of where its activation occurs, which upstream regulators are involved in the activation/inactivation cycle and the GTPase interacting partners that determine the intracellular niche and extent of signaling. Data discussed here unravel unparalleled cooperation and coordination of functions among GTPases and their regulators in supporting strong adhesion between cells.

摘要

许多有趣的报告强调了协调细胞-细胞接触形成和维持的信号蛋白复杂网络。我们还有很多需要了解的是,体外结合数据如何转化为细胞内蛋白质的相互作用,以及这种相互作用是否调节蛋白质的信号转导特性。最近的研究表明,重要的是要仔细考虑小 GTPase 的激活情况,包括其激活发生的位置、参与激活/失活循环的上游调节剂以及决定细胞内位置和信号转导程度的与 GTPase 相互作用的伙伴。这里讨论的数据揭示了 GTPase 及其调节剂在支持细胞间强粘附方面的功能无与伦比的合作和协调。