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本文引用的文献

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Signaling networks that regulate cell migration.调节细胞迁移的信号网络。
Cold Spring Harb Perspect Biol. 2015 Aug 3;7(8):a005959. doi: 10.1101/cshperspect.a005959.
2
Wnt signaling.Wnt 信号通路。
Cold Spring Harb Perspect Biol. 2012 May 1;4(5):a011163. doi: 10.1101/cshperspect.a011163.
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Wnt signaling in cancer.Wnt 信号通路与癌症。
Cold Spring Harb Perspect Biol. 2012 May 1;4(5):a008052. doi: 10.1101/cshperspect.a008052.
4
Willin and Par3 cooperatively regulate epithelial apical constriction through aPKC-mediated ROCK phosphorylation.威尔蛋白和 Par3 通过蛋白激酶 C 介导的 ROCK 磷酸化协同调节上皮细胞顶端缢缩。
Nat Cell Biol. 2011 Jun 19;13(7):860-6. doi: 10.1038/ncb2274.
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Role of YAP/TAZ in mechanotransduction.YAP/TAZ 在机械转导中的作用。
Nature. 2011 Jun 8;474(7350):179-83. doi: 10.1038/nature10137.
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α-catenin is a tumor suppressor that controls cell accumulation by regulating the localization and activity of the transcriptional coactivator Yap1.α-连环蛋白是一种肿瘤抑制因子,通过调节转录共激活因子 Yap1 的定位和活性来控制细胞积累。
Sci Signal. 2011 May 24;4(174):ra33. doi: 10.1126/scisignal.2001823.
7
PAR proteins diffuse freely across the anterior-posterior boundary in polarized C. elegans embryos.PAR 蛋白在极化的秀丽隐杆线虫胚胎中自由扩散穿过前后边界。
J Cell Biol. 2011 May 2;193(3):583-94. doi: 10.1083/jcb.201011094. Epub 2011 Apr 25.
8
KIBRA suppresses apical exocytosis through inhibition of aPKC kinase activity in epithelial cells.KIBRA 通过抑制上皮细胞中 aPKC 激酶活性来抑制顶端胞吐作用。
Curr Biol. 2011 Apr 26;21(8):705-11. doi: 10.1016/j.cub.2011.03.029. Epub 2011 Apr 14.
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Yap1 acts downstream of α-catenin to control epidermal proliferation.Yap1 在 α-连环蛋白下游发挥作用,控制表皮细胞增殖。
Cell. 2011 Mar 4;144(5):782-95. doi: 10.1016/j.cell.2011.02.031.
10
The Crumbs complex couples cell density sensing to Hippo-dependent control of the TGF-β-SMAD pathway.Crumb 复合物将细胞密度感应与 Hippo 依赖性 TGF-β-SMAD 通路的控制联系起来。
Dev Cell. 2010 Dec 14;19(6):831-44. doi: 10.1016/j.devcel.2010.11.012.

细胞极性中的信号通路。

Signaling pathways in cell polarity.

机构信息

Department of Oncology, Rosalind and Morris Goodman Cancer Research Centre, McGill University, Montreal, Quebec, Canada.

出版信息

Cold Spring Harb Perspect Biol. 2012 Jun 1;4(6):a009654. doi: 10.1101/cshperspect.a009654.

DOI:10.1101/cshperspect.a009654
PMID:22553378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3367552/
Abstract

A key function of signal transduction during cell polarization is the creation of spatially segregated regions of the cell cortex that possess different lipid and protein compositions and have distinct functions. Polarity can be initiated spontaneously or in response to signaling inputs from adjacent cells or soluble factors and is stabilized by positive-feedback loops. A conserved group of proteins, the Par proteins, plays a central role in polarity establishment and maintenance in many contexts. These proteins generate and maintain their distinct locations in cells by actively excluding one another from specific regions of the plasma membrane. The Par signaling pathway intersects with multiple other pathways that control cell growth, death, and organization.

摘要

细胞极化过程中信号转导的一个关键功能是创建细胞皮质的空间分隔区域,这些区域具有不同的脂质和蛋白质组成,并具有不同的功能。极性可以自发形成,也可以响应来自相邻细胞或可溶性因子的信号输入,并且通过正反馈环稳定。一组保守的蛋白质,即 Par 蛋白,在许多情况下在极性建立和维持中起着核心作用。这些蛋白质通过主动将彼此排除在质膜的特定区域之外,从而在细胞中产生并维持它们的独特位置。Par 信号通路与控制细胞生长、死亡和组织的多个其他通路相交。