Identification and expression analysis of the human μ-protocadherin gene in fetal and adult kidneys

被引:24
作者
Goldberg, M
Wei, M
Tycko, B
Falikovich, I
Warburton, D
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pediat, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ Coll Phys & Surg, Inst Canc Genet, New York, NY 10032 USA
关键词
cell adhesion; apical targeting;
D O I
10.1152/ajprenal.00012.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We recently cloned mu-protocadherin, a developmentally regulated cell adhesion molecule that contains an extracellular region with four cadherin-like ectodomains and a triply repeating mucin domain in its longer isoform. Expression of mu-protocadherin in L929 cells resulted in cellular aggregation, confirming its role in intercellular adhesion. We now identify the human mu-protocadherin ortholog and study its distribution in vivo and its targeting in polarized epithelia. Basic Local Alignment Search Tool searches and fluorescent in situ hybridization analysis on the basis of human-mouse synteny reveal that mu-protocadherin maps to 11p15.5, matching a previously identified gene called MUCDHL. At least three different splicing isoforms exist for MUCDHL that vary in expression in the fetal kidney. mu-Protocadherin is apically expressed along the brush border of the proximal convoluted tubule of the adult kidney. Transfection of truncated forms of mu-protocadherin into polarized Madin-Darby canine kidney cells reveals that the NH2 terminus is essential for targeting to the apical surface. These results suggest that although human mu-protocadherin may mediate a homotypic adhesive interaction, it may have additional functions in terminally differentiated epithelia.
引用
收藏
页码:F454 / F463
页数:10
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