• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

细胞极性信号通路的相互作用。

Crosstalk of cell polarity signaling pathways.

作者信息

Mazel Tomáš

机构信息

Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00, Prague 2, Czech Republic.

State Institute for Drug Control, Šrobárova 48, 100 41, Prague 10, Czech Republic.

出版信息

Protoplasma. 2017 May;254(3):1241-1258. doi: 10.1007/s00709-017-1075-2. Epub 2017 Mar 14.

DOI:10.1007/s00709-017-1075-2
PMID:28293820
Abstract

Cell polarity, the asymmetric organization of cellular components along one or multiple axes, is present in most cells. From budding yeast cell polarization induced by pheromone signaling, oocyte polarization at fertilization to polarized epithelia and neuronal cells in multicellular organisms, similar mechanisms are used to determine cell polarity. Crucial role in this process is played by signaling lipid molecules, small Rho family GTPases and Par proteins. All these signaling circuits finally govern the cytoskeleton, which is responsible for oriented cell migration, cell shape changes, and polarized membrane and organelle trafficking. Thus, typically in the process of cell polarization, most cellular constituents become polarized, including plasma membrane lipid composition, ion concentrations, membrane receptors, and proteins in general, mRNA, vesicle trafficking, or intracellular organelles. This review gives a brief overview how these systems talk to each other both during initial symmetry breaking and within the signaling feedback loop mechanisms used to preserve the polarized state.

摘要

细胞极性,即细胞成分沿一个或多个轴的不对称组织,存在于大多数细胞中。从信息素信号诱导的芽殖酵母细胞极化、受精时的卵母细胞极化到多细胞生物中的极化上皮细胞和神经元细胞,都使用类似的机制来确定细胞极性。信号脂质分子、小Rho家族GTP酶和Par蛋白在这一过程中发挥着关键作用。所有这些信号通路最终控制着细胞骨架,细胞骨架负责定向细胞迁移、细胞形状变化以及极化的膜和细胞器运输。因此,在细胞极化过程中,通常大多数细胞成分都会发生极化,包括质膜脂质组成、离子浓度、膜受体以及一般的蛋白质、mRNA、囊泡运输或细胞内细胞器。本综述简要概述了这些系统在初始对称性破坏期间以及用于维持极化状态的信号反馈回路机制中是如何相互作用的。

相似文献

1
Crosstalk of cell polarity signaling pathways.细胞极性信号通路的相互作用。
Protoplasma. 2017 May;254(3):1241-1258. doi: 10.1007/s00709-017-1075-2. Epub 2017 Mar 14.
2
Rho GTPases at the crossroad of signaling networks in mammals: impact of Rho-GTPases on microtubule organization and dynamics.Rho GTP酶在哺乳动物信号网络的交叉路口:Rho GTP酶对微管组织和动力学的影响
Small GTPases. 2014;5:e28430. doi: 10.4161/sgtp.28430. Epub 2014 Mar 20.
3
Roles of IQGAP1 in cell polarization and migration.IQGAP1在细胞极化和迁移中的作用。
Novartis Found Symp. 2005;269:92-101; discussion 101-5, 223-30.
4
Roles of Rho-family GTPases in cell polarisation and directional migration.Rho家族小GTP酶在细胞极化和定向迁移中的作用。
Curr Opin Cell Biol. 2003 Oct;15(5):590-7. doi: 10.1016/s0955-0674(03)00097-8.
5
Directional cell migration regulation by small G proteins, nectin-like molecule-5, and afadin.小 G 蛋白、神经钙黏蛋白样分子 5 和 afadin 对定向细胞迁移的调节作用。
Int Rev Cell Mol Biol. 2011;287:97-143. doi: 10.1016/B978-0-12-386043-9.00003-7.
6
Cell polarity signaling in Arabidopsis.拟南芥中的细胞极性信号传导
Annu Rev Cell Dev Biol. 2008;24:551-75. doi: 10.1146/annurev.cellbio.23.090506.123233.
7
IQGAP1: a key regulator of adhesion and migration.IQGAP1:黏附与迁移的关键调节因子。
J Cell Sci. 2005 May 15;118(Pt 10):2085-92. doi: 10.1242/jcs.02379.
8
Cell motility: can Rho GTPases and microtubules point the way?细胞运动性:Rho GTP酶和微管能指明方向吗?
J Cell Sci. 2001 Nov;114(Pt 21):3795-803. doi: 10.1242/jcs.114.21.3795.
9
Epithelial cell shape and Rho small GTPases.上皮细胞形态与Rho小GTP酶
Novartis Found Symp. 2005;269:144-55; discussion 155-8, 223-30.
10
Microtubules meet substrate adhesions to arrange cell polarity.微管与底物黏附接触以排列细胞极性。
Curr Opin Cell Biol. 2003 Feb;15(1):40-7. doi: 10.1016/s0955-0674(02)00008-x.

引用本文的文献

1
Downregulation of connexin 43 is crucial for basal cell alignment in ameloblastoma and odontogenic keratocyst.连接蛋白43的下调对于成釉细胞瘤和牙源性角化囊肿中基底细胞的排列至关重要。
Saudi Dent J. 2024 Jul;36(7):990-994. doi: 10.1016/j.sdentj.2024.05.003. Epub 2024 May 8.
2
Role of connexin 43 in odontoblastic differentiation and structural maintenance in pulp damage repair.缝隙连接蛋白 43 在牙髓损伤修复中牙本质细胞分化和结构维持中的作用。
Int J Oral Sci. 2021 Jan 8;13(1):1. doi: 10.1038/s41368-020-00105-1.
3
[Polarity of ameloblasts and odontoblasts and their related regulators].

本文引用的文献

1
Intermediate Filaments and Polarization in the Intestinal Epithelium.肠上皮中的中间丝与极化
Cells. 2016 Jul 15;5(3):32. doi: 10.3390/cells5030032.
2
Origins of the cytolytic synapse.细胞溶解突触的起源。
Nat Rev Immunol. 2016 Jul;16(7):421-32. doi: 10.1038/nri.2016.54. Epub 2016 Jun 6.
3
Role of the epithelial cell-specific clathrin adaptor complex AP-1B in cell polarity.上皮细胞特异性网格蛋白衔接复合体AP-1B在细胞极性中的作用。
[成釉细胞和成牙本质细胞的极性及其相关调节因子]
Hua Xi Kou Qiang Yi Xue Za Zhi. 2019 Jun 1;37(3):309-313. doi: 10.7518/hxkq.2019.03.016.
4
FRET biosensor allows spatio-temporal observation of shear stress-induced polar RhoGDIα activation.荧光共振能量转移生物传感器可对剪切应力诱导的极性RhoGDIα激活进行时空观察。
Commun Biol. 2018 Dec 10;1:224. doi: 10.1038/s42003-018-0232-2. eCollection 2018.
5
Mutual inhibition between PTEN and PIP3 generates bistability for polarity in motile cells.PTEN 和 PIP3 之间的相互抑制为游动细胞的极性产生双稳定性。
Nat Commun. 2018 Oct 26;9(1):4481. doi: 10.1038/s41467-018-06856-0.
6
Mechanism of drug extrusion by brain endothelial cells via lysosomal drug trapping and disposal by neutrophils.脑内皮细胞通过溶酶体药物捕获和中性粒细胞处置将药物挤出细胞的机制。
Proc Natl Acad Sci U S A. 2018 Oct 9;115(41):E9590-E9599. doi: 10.1073/pnas.1719642115. Epub 2018 Sep 25.
7
Regulation of Polarity Protein Levels in the Developing Central Nervous System.发育中中枢神经系统中极性蛋白水平的调节。
J Mol Biol. 2018 Sep 28;430(19):3472-3480. doi: 10.1016/j.jmb.2018.05.036. Epub 2018 Jun 1.
8
Formin 2 Regulates Lysosomal Degradation of Wnt-Associated β-Catenin in Neural Progenitors.formin 2 通过调控神经祖细胞中 Wnt 相关 β-连环蛋白的溶酶体降解来发挥作用。
Cereb Cortex. 2019 May 1;29(5):1938-1952. doi: 10.1093/cercor/bhy073.
9
Editorial.
Protoplasma. 2017 May;254(3):1141-1142. doi: 10.1007/s00709-017-1093-0. Epub 2017 Mar 16.
Cell Logist. 2015 Jul 30;5(2):e1074331. doi: 10.1080/21592799.2015.1074331. eCollection 2015 Apr-Jun.
4
Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development.在组织修复和大脑发育中将初级纤毛与细胞迁移联系起来。
Bioscience. 2014 Dec 1;64(12):1115-1125. doi: 10.1093/biosci/biu179. Epub 2014 Nov 25.
5
Gβ Regulates Coupling between Actin Oscillators for Cell Polarity and Directional Migration.Gβ调节肌动蛋白振荡器之间的偶联以实现细胞极性和定向迁移。
PLoS Biol. 2016 Feb 18;14(2):e1002381. doi: 10.1371/journal.pbio.1002381. eCollection 2016 Feb.
6
The Golgin Family of Coiled-Coil Tethering Proteins.卷曲螺旋蛋白 tethering 蛋白家族的 Golgin 家族。
Front Cell Dev Biol. 2016 Jan 11;3:86. doi: 10.3389/fcell.2015.00086. eCollection 2015.
7
Miro sculpts mitochondrial dynamics in neuronal health and disease.Miro 塑造神经元健康和疾病中线粒体动力学。
Neurobiol Dis. 2016 Jun;90:27-34. doi: 10.1016/j.nbd.2015.12.008. Epub 2015 Dec 19.
8
Cdc42 and Cellular Polarity: Emerging Roles at the Golgi.Cdc42与细胞极性:在高尔基体中的新作用
Trends Cell Biol. 2016 Apr;26(4):241-248. doi: 10.1016/j.tcb.2015.11.003. Epub 2015 Dec 17.
9
Locally excitable Cdc42 signals steer cells during chemotaxis.局部可兴奋的Cdc42信号在趋化作用过程中引导细胞。
Nat Cell Biol. 2016 Feb;18(2):191-201. doi: 10.1038/ncb3292. Epub 2015 Dec 21.
10
Spontaneous cell polarization: Feedback control of Cdc42 GTPase breaks cellular symmetry.自发细胞极化:Cdc42 GTP酶的反馈控制打破细胞对称性。
Bioessays. 2015 Nov;37(11):1193-201. doi: 10.1002/bies.201500077. Epub 2015 Sep 4.