Terminal Differentiation in Epithelia: The Role of Integrins in Hensin Polymerization

被引:31
作者
Al-Awqati, Qais [1 ,2 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Physiol & Cellular Biophys, New York, NY 10032 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 73 | 2011年 / 73卷
关键词
DMBT1; intercalated cells; acid-base; EXTRACELLULAR-MATRIX; INTERCALATED CELLS; COLUMNAR EPITHELIA; H+-ATPASE; ACID; ACTIVATION; POLARITY; BETA-1-INTEGRIN; CYCLOPHILIN; EXPRESSION;
D O I
10.1146/annurev-physiol-012110-142253
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Epithelia, the most abundant cell type, differentiate to protoepithelia from stem cells by developing apical and basolateral membrane domains and form sheets of cells connected by junctions. Following this differentiation step, the cells undergo a second step (terminal differentiation), during which they acquire a mature phenotype, which unlike the protoepithelial one is tissue and organ specific. An extracellular matrix (ECM) protein termed hensin (DMBT1) mediates this differentiation step in the kidney intercalated cells. Although hensin is secreted as a soluble monomer, it requires polymerization and deposition in the ECM to become active. The polymerization step is mediated by the activation of inside-out signaling by integrins and by the secretion of two proteins: cypA (a cis-trans prolyl isomerase) and galectin 3.
引用
收藏
页码:401 / 412
页数:12
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