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本文引用的文献

1
Setting up a selective barrier at the apical junction complex.在顶端连接复合体处建立一个选择性屏障。
Curr Opin Cell Biol. 2004 Apr;16(2):140-5. doi: 10.1016/j.ceb.2004.01.005.
2
Breaking into the epithelial apical-junctional complex--news from pathogen hackers.突破上皮顶端连接复合体——病原体侵袭的新进展
Curr Opin Cell Biol. 2004 Feb;16(1):86-93. doi: 10.1016/j.ceb.2003.12.002.
3
A peculiar internalization of claudins, tight junction-specific adhesion molecules, during the intercellular movement of epithelial cells.在上皮细胞的细胞间移动过程中,紧密连接特异性黏附分子claudins出现了一种特殊的内化现象。
J Cell Sci. 2004 Mar 1;117(Pt 7):1247-57. doi: 10.1242/jcs.00972.
4
Involvement of the junctional adhesion molecule-1 (JAM1) homodimer interface in regulation of epithelial barrier function.连接粘附分子1(JAM1)同型二聚体界面参与上皮屏障功能的调节。
J Biol Chem. 2004 Apr 16;279(16):16254-62. doi: 10.1074/jbc.M309483200. Epub 2004 Jan 28.
5
CRB3 binds directly to Par6 and regulates the morphogenesis of the tight junctions in mammalian epithelial cells.CRB3直接与Par6结合,并调节哺乳动物上皮细胞中紧密连接的形态发生。
Mol Biol Cell. 2004 Mar;15(3):1324-33. doi: 10.1091/mbc.e03-04-0235. Epub 2004 Jan 12.
6
Mechanism of recruiting Sec6/8 (exocyst) complex to the apical junctional complex during polarization of epithelial cells.上皮细胞极化过程中Sec6/8(外泌体)复合物募集至顶端连接复合物的机制。
J Cell Sci. 2004 Feb 1;117(Pt 4):559-70. doi: 10.1242/jcs.00893. Epub 2004 Jan 6.
7
Comprehensive proteomic analysis of human Par protein complexes reveals an interconnected protein network.对人类Par蛋白复合物的全面蛋白质组学分析揭示了一个相互连接的蛋白质网络。
J Biol Chem. 2004 Mar 26;279(13):12804-11. doi: 10.1074/jbc.M312171200. Epub 2003 Dec 15.
8
Junctional adhesion molecules (JAMs): more molecules with dual functions?连接黏附分子(JAMs):更多具有双重功能的分子?
J Cell Sci. 2004 Jan 1;117(Pt 1):19-29. doi: 10.1242/jcs.00930.
9
Junctional complexes in various epithelia.各种上皮组织中的连接复合体。
J Cell Biol. 1963 May;17(2):375-412. doi: 10.1083/jcb.17.2.375.
10
Reversal of charge selectivity in cation or anion-selective epithelial lines by expression of different claudins.通过表达不同的紧密连接蛋白,使阳离子或阴离子选择性上皮细胞系中的电荷选择性发生逆转。
Am J Physiol Renal Physiol. 2003 Dec;285(6):F1078-84. doi: 10.1152/ajprenal.00116.2003. Epub 2003 Sep 16.

上皮顶端连接复合体的分级分离:对不同亚结构中蛋白质分布的重新评估。

Fractionation of the epithelial apical junctional complex: reassessment of protein distributions in different substructures.

作者信息

Vogelmann Roger, Nelson W James

机构信息

Department of Molecular and Cellular Physiology, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5435, USA.

出版信息

Mol Biol Cell. 2005 Feb;16(2):701-16. doi: 10.1091/mbc.e04-09-0827. Epub 2004 Nov 17.

DOI:10.1091/mbc.e04-09-0827
PMID:15548593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC545905/
Abstract

The epithelial apical junctional complex (AJC) is an important regulator of cell structure and function. The AJC is compartmentalized into substructures comprising the tight and adherens junctions, and other membrane complexes containing the membrane proteins nectin, junctional adhesion molecule, and crumbs. In addition, many peripheral membrane proteins localize to the AJC. Studies of isolated proteins indicate a complex map of potential binding partners in which there is extensive overlap in the interactions between proteins in different AJC substructures. As an alternative to a direct search for specific protein-protein interactions, we sought to separate membrane substructures of the AJC in iodixanol density gradients and define their protein constituents. Results show that the AJC can be fractured into membrane substructures that contain specific membrane and peripheral membrane proteins. The composition of each substructure reveals a more limited overlap in common proteins than predicted from the inventory of potential interactions; some of the overlapping proteins may be involved in stepwise recruitment and assembly of AJC substructures.

摘要

上皮顶端连接复合体(AJC)是细胞结构和功能的重要调节因子。AJC被分隔成包含紧密连接和黏着连接的亚结构,以及其他含有膜蛋白nectin、连接黏附分子和crumbs的膜复合体。此外,许多外周膜蛋白定位于AJC。对分离蛋白的研究表明存在一个潜在结合伙伴的复杂图谱,其中不同AJC亚结构中的蛋白之间的相互作用存在广泛重叠。作为直接寻找特定蛋白质-蛋白质相互作用的替代方法,我们试图在碘克沙醇密度梯度中分离AJC的膜亚结构,并确定其蛋白质成分。结果表明,AJC可断裂成包含特定膜蛋白和外周膜蛋白的膜亚结构。每个亚结构的组成显示,共同蛋白的重叠比根据潜在相互作用清单预测的要有限;一些重叠蛋白可能参与AJC亚结构的逐步募集和组装。