Tight junctions and the regulation of gene expression

被引:207
作者
Balda, Maria S. [1 ]
Matter, Karl [1 ]
机构
[1] UCL, Inst Ophthalmol, Div Cell Biol, London EC1V 9EL, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2009年 / 1788卷 / 04期
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
ZO-1; ZO-2; ZO-3; ZONAB; DbpA; Cell cycle; Cyclin D1; PCNA; erbB-2; CDK4; Apg-2; Symplekin RalA; Occludin Claudin; JAM; Cingulin GEF-H1; Beta-catenin; E-cadherin; VE-cadherin; Ras; TGF-beta; Snail; Slug; Glucocorticoid; Gene methylation; Epithelial-mesenchymal transition; MAMMARY EPITHELIAL-CELLS; TUMOR-SUPPRESSOR PROTEIN; EPIDERMAL-GROWTH-FACTOR; NUCLEAR ANTIGEN PCNA; CYCLIN D1 GENE; BETA-CATENIN; ZONULA OCCLUDENS-1; TRANSCRIPTION FACTORS; BARRIER FUNCTION; UP-REGULATION;
D O I
10.1016/j.bbamem.2008.11.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell adhesion is a key regulator of cell differentiation. Cell interactions with neighboring cells and the extracellular matrix regulate gene expression, cell proliferation, polarity and apoptosis. Apical cell-cell junctions participate in these processes using different types of proteins, some of them exhibit nuclear and junctional localization and are called NACos for Nuclear Adhesion Complexes. Tight junctions are one type of such cell-cell junctions and several signaling complexes have been identified to associate with them. In general, expression of tight junction components suppresses proliferation to allow differentiation in a coordinated manner with adherens junctions and extracellular matrix adhesion. These tight junction components have been shown to affect several signaling and transcriptional pathways, and changes in the expression of tight junction proteins are associated with several disease conditions, such as cancer. Here, we will review how tight junction proteins participate in the regulation of gene expression and cell proliferation, as well as how they are regulated themselves by different mechanisms involved in gene expression and cell differentiation. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:761 / 767
页数:7
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