Membrane proteins follow multiple pathways to the basolateral cell surface in polarized epithelial cells

被引:64
|
作者
Farr, Glen A. [1 ,2 ]
Hull, Michael [1 ,2 ]
Mellman, Ira [3 ]
Caplan, Michael J. [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
[3] Genentech Inc, San Francisco, CA 94080 USA
来源
JOURNAL OF CELL BIOLOGY | 2009年 / 186卷 / 02期
基金
美国国家卫生研究院;
关键词
DARBY CANINE KIDNEY; RETINAL-PIGMENT EPITHELIUM; ION-TRANSPORT PROTEINS; E-CADHERIN TRAFFICKING; NA-K-ATPASE; MDCK CELLS; PLASMA-MEMBRANE; RECYCLING ENDOSOMES; ALPHA-SUBUNIT; GOLGI NETWORK;
D O I
10.1083/jcb.200901021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Newly synthesized apical and basolateral membrane proteins are sorted from one another in polarized epithelial cells. The trans-Golgi network participates in this sorting process, but some basolateral proteins travel from the Golgi to recycling endosomes (REs) before their surface delivery. Using a novel system for pulse-chase microscopy, we have visualized the postsynthetic route pursued by a newly synthesized cohort of Na, K-ATPase. We find that the basolateral delivery of newly synthesized Na, K-ATPase occurs via a pathway distinct from that pursued by the vesicular stomatitis virus G protein (VSV-G). Na, KATPase surface delivery occurs at a faster rate than that observed for VSV-G. The Na, K-ATPase does not pass through the RE compartment en route to the plasma membrane, and Na, K-ATPase trafficking is not regulated by the same small GTPases as other basolateral proteins. Finally, Na, K-ATPase and VSV-G travel in separate post-Golgi transport intermediates, demonstrating directly that multiple routes exist for transport from the Golgi to the basolateral membrane in polarized epithelial cells.
引用
收藏
页码:269 / 282
页数:14
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