• 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

Par3/Par6/aPKC 复合物与上皮细胞极性。

The Par3/Par6/aPKC complex and epithelial cell polarity.

机构信息

Division of Life Science, State Key Laboratory of Molecular Neuroscience, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.

出版信息

Exp Cell Res. 2013 Jun 10;319(10):1357-64. doi: 10.1016/j.yexcr.2013.03.021. Epub 2013 Mar 25.

DOI:10.1016/j.yexcr.2013.03.021
PMID:23535009
Abstract

Apical-basal polarity is the basic organizing principle of epithelial cells, and endows epithelial cells to function as defensive barriers and as mediators of vectorial transport of nutrients in and out of organisms. Apical-basal polarity is controlled by a number of conserved polarity factors that regulate cytoskeletal organizations, asymmetric distributions of cellular components, and directional transports across cells. Polarity factors often occupy specific membrane regions in response to the adhesion forces generated by cell-cell and cell-extracellular matrix interactions. Both internal polarity factors and the external extracellular matrices play fundamental roles in epithelial cell polarity establishment and maintenance. This review focuses on recent developments of the Par3/Par6/aPKC complex and its interacting proteins in epithelial cell polarity.

摘要

顶端-基底极性是上皮细胞的基本组织原则,使上皮细胞能够作为防御屏障,并作为营养物质在生物体内外的载体运输的介质。顶端-基底极性由许多保守的极性因子控制,这些因子调节细胞骨架组织、细胞成分的不对称分布和细胞内的定向运输。极性因子通常在响应细胞-细胞和细胞-细胞外基质相互作用产生的粘附力时,占据特定的膜区域。内部极性因子和外部细胞外基质在建立和维持上皮细胞极性方面都起着至关重要的作用。本综述重点介绍了 Par3/Par6/aPKC 复合物及其在上皮细胞极性中的相互作用蛋白的最新进展。

相似文献

1
The Par3/Par6/aPKC complex and epithelial cell polarity.Par3/Par6/aPKC 复合物与上皮细胞极性。
Exp Cell Res. 2013 Jun 10;319(10):1357-64. doi: 10.1016/j.yexcr.2013.03.021. Epub 2013 Mar 25.
2
aPKC Inhibition by Par3 CR3 Flanking Regions Controls Substrate Access and Underpins Apical-Junctional Polarization.Par3 CR3侧翼区域对非典型蛋白激酶C的抑制作用控制底物进入并支撑顶端连接极性。
Dev Cell. 2016 Aug 22;38(4):384-98. doi: 10.1016/j.devcel.2016.07.018.
3
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.
4
Magi Is Associated with the Par Complex and Functions Antagonistically with Bazooka to Regulate the Apical Polarity Complex.Magi与Par复合体相关,并与Bazooka起拮抗作用以调节顶端极性复合体。
PLoS One. 2016 Apr 13;11(4):e0153259. doi: 10.1371/journal.pone.0153259. eCollection 2016.
5
PAR3-PAR6-atypical PKC polarity complex proteins in neuronal polarization.神经元极化中的 PAR3-PAR6-非典型 PKC 极性复合物蛋白。
Cell Mol Life Sci. 2018 Aug;75(15):2735-2761. doi: 10.1007/s00018-018-2828-6. Epub 2018 Apr 25.
6
Direct interaction of two polarity complexes implicated in epithelial tight junction assembly.参与上皮紧密连接组装的两种极性复合物的直接相互作用。
Nat Cell Biol. 2003 Feb;5(2):137-42. doi: 10.1038/ncb923.
7
Disruption of the Cdc42/Par6/aPKC or Dlg/Scrib/Lgl Polarity Complex Promotes Epithelial Proliferation via Overlapping Mechanisms.Cdc42/Par6/aPKC或Dlg/Scrib/Lgl极性复合体的破坏通过重叠机制促进上皮细胞增殖。
PLoS One. 2016 Jul 25;11(7):e0159881. doi: 10.1371/journal.pone.0159881. eCollection 2016.
8
A picket fence function for adherens junctions in epithelial cell polarity.上皮细胞极性中黏着连接的栅栏功能。
Cells Dev. 2021 Dec;168:203719. doi: 10.1016/j.cdev.2021.203719. Epub 2021 Jul 7.
9
Polarity proteins PAR6 and aPKC regulate cell death through GSK-3beta in 3D epithelial morphogenesis.极性蛋白PAR6和非典型蛋白激酶C在三维上皮形态发生过程中通过糖原合成酶激酶-3β调节细胞死亡。
J Cell Sci. 2007 Jul 15;120(Pt 14):2309-17. doi: 10.1242/jcs.007443.
10
Structural basis for the interaction between the cell polarity proteins Par3 and Par6.细胞极性蛋白 Par3 和 Par6 相互作用的结构基础。
Sci Signal. 2018 Feb 13;11(517):eaam9899. doi: 10.1126/scisignal.aam9899.

引用本文的文献

1
Emerging regulatory mechanisms and functions of biomolecular condensates: implications for therapeutic targets.生物分子凝聚物的新兴调控机制与功能:对治疗靶点的启示
Signal Transduct Target Ther. 2025 Jan 6;10(1):4. doi: 10.1038/s41392-024-02070-1.
2
A PDZ-kinase allosteric relay mediates Par complex regulator exchange.一种PDZ激酶变构中继介导Par复合物调节剂交换。
J Biol Chem. 2025 Feb;301(2):108097. doi: 10.1016/j.jbc.2024.108097. Epub 2024 Dec 18.
3
A PDZ-kinase allosteric relay mediates Par complex regulator exchange.一种PDZ激酶变构中继介导Par复合物调节因子交换。
bioRxiv. 2024 Oct 19:2024.10.18.619144. doi: 10.1101/2024.10.18.619144.
4
Crosstalk of MAP3K1 and EGFR signaling mediates gene-environment interactions that block developmental tissue closure.MAP3K1 和 EGFR 信号的串扰介导了阻止发育组织闭合的基因-环境相互作用。
J Biol Chem. 2024 Jul;300(7):107486. doi: 10.1016/j.jbc.2024.107486. Epub 2024 Jun 18.
5
Ameloblastin and its multifunctionality in amelogenesis: A review.成釉蛋白及其在釉质发生中的多功能性:综述。
Matrix Biol. 2024 Aug;131:62-76. doi: 10.1016/j.matbio.2024.05.007. Epub 2024 May 28.
6
Synthetic Par polarity induces cytoskeleton asymmetry in unpolarized mammalian cells.人工 Par 极性诱导非极化哺乳动物细胞中的细胞骨架不对称性。
Cell. 2023 Oct 12;186(21):4710-4727.e35. doi: 10.1016/j.cell.2023.08.034. Epub 2023 Sep 28.
7
Scribble, Lgl1, and myosin IIA interact with α-/β-catenin to maintain epithelial junction integrity.Scribble、Lgl1 和肌球蛋白 IIA 与α-/β-连环蛋白相互作用,以维持上皮连接的完整性。
Cell Adh Migr. 2023 Dec;17(1):1-23. doi: 10.1080/19336918.2023.2260645. Epub 2023 Sep 24.
8
Nox1-based NADPH oxidase regulates the Par protein complex activity to control cell polarization.基于Nox1的NADPH氧化酶调节Par蛋白复合体活性以控制细胞极化。
Front Cell Dev Biol. 2023 Aug 11;11:1231489. doi: 10.3389/fcell.2023.1231489. eCollection 2023.
9
The effect of Par3 on the cellular junctions and biological functions of odontoblast-lineage cells.Par3 对成牙本质细胞系细胞的细胞连接和生物学功能的影响。
Odontology. 2024 Jan;112(1):125-137. doi: 10.1007/s10266-023-00838-5. Epub 2023 Jul 26.
10
Overview of junctional complexes during mammalian early embryonic development.哺乳动物胚胎早期发育中连接复合体的概述。
Front Endocrinol (Lausanne). 2023 Apr 20;14:1150017. doi: 10.3389/fendo.2023.1150017. eCollection 2023.