Trafficking to the Apical and Basolateral Membranes in Polarized Epithelial Cells

被引:78
|
作者
Stoops, Emily H.
Caplan, Michael J. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
来源
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
DARBY CANINE KIDNEY; RETINAL-PIGMENT EPITHELIUM; GPI-ANCHORED PROTEINS; INFLUENZA-VIRUS HEMAGGLUTININ; NA+-K+-ATPASE; NEPHROGENIC DIABETES-INSIPIDUS; INTESTINAL SUCRASE-ISOMALTASE; MANNOSE 6-PHOSPHATE RECEPTOR; RESPIRATORY SYNCYTIAL VIRUS; LYSOSOMAL ACID-PHOSPHATASE;
D O I
10.1681/ASN.2013080883
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Renal epithelial cells must maintain distinct protein compositions in their apical and basolateral membranes in order to perform their transport functions. The creation of these polarized protein distributions depends on sorting signals that designate the trafficking route and site of ultimate functional residence for each protein. Segregation of newly synthesized apical and basolateral proteins into distinct carrier vesicles can occur at the trans-Golgi network, recycling endosomes, or a growing assortment of stations along the cellular trafficking pathway. The nature of the specific sorting signal and the mechanism through which it is interpreted can influence the route a protein takes through the cell. Cell type specific variations in the targeting motifs of a protein, as are evident for Na,K-ATPase, demonstrate a remarkable capacity to adapt sorting pathways to different developmental states or physiologic requirements. This review summarizes our current understanding of apical and basolateral trafficking routes in polarized epithelial cells.
引用
收藏
页码:1375 / 1386
页数:12
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