Journal article
Epithelial cell polarity: new perspectives
Seminars in nephrology, Vol.15(4), pp.272-284
07/1995
PMID: 7569407
Abstract
All epithelial cells possess two distinct plasma membrane domains. The apical and basolateral domains differ in protein and lipid composition, and this allows the cell to perform a variety of vectorial functions. Structures involved in generating and maintaining these distinct membrane domains include the tight junction, which serves to restrict lateral diffusion within the membrane, and the cortical cytoskeleton, which can selectively bind and retain transmembrane proteins at a particular surface. A major means to generating membrane asymmetry lies in the ability of the cell to sort apical and basolateral proteins and target them to appropriate destinations. This sorting occurs predominantly at two intracellular sites: the trans-Golgi network, and the basolateral endosome. Constitutive protein traffic in epithelial cells has recently been shown to be regulated via classical signal transduction pathways involving heterotrimeric G proteins and protein kinases. The diversion of apical and basolateral proteins into specific pathways can be mediated by signals contained within these proteins. Apical sorting information is thought to be localized in the luminal domain of transmembrane proteins, and in the case of proteins anchored to the membrane via a GPI anchor, apical sorting information is provided by the lipid moiety. In contrast, basolateral signals have been identified in the cytoplasmic domain of transmembrane proteins. Shared similarities between basolateral signals and those required for endocytosis have suggested that these two sorting processes are mechanistically related.
Details
- Title: Subtitle
- Epithelial cell polarity: new perspectives
- Creators
- A H Le Gall - Department of Cell Biology and Anatomy, Cornell University Medical College, New York, NY 10021, USAC YeamanA MueschE Rodriguez-Boulan
- Resource Type
- Journal article
- Publication Details
- Seminars in nephrology, Vol.15(4), pp.272-284
- Publisher
- United States
- PMID
- 7569407
- ISSN
- 0270-9295
- eISSN
- 1558-4488
- Grant note
- GM41771-05 / NIGMS NIH HHS GM34107-11 / NIGMS NIH HHS R01 GM034107 / NIGMS NIH HHS EY08538-02 / NEI NIH HHS
- Language
- English
- Date published
- 07/1995
- Academic Unit
- Anatomy and Cell Biology; Internal Medicine
- Record Identifier
- 9984025596302771
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