Hartman Institute for Therapeutic Organ Regeneration

Clathrin is a key regulator of basolateral polarity.

TitleClathrin is a key regulator of basolateral polarity.
Publication TypeJournal Article
Year of Publication2008
AuthorsDeborde S, Perret E, Gravotta D, Deora A, Salvarezza S, Schreiner R, Rodriguez-Boulan E
JournalNature
Volume452
Issue7188
Pagination719-23
Date Published2008 Apr 10
ISSN1476-4687
KeywordsAnimals, Cathepsin D, Cell Line, Cell Polarity, Clathrin, Clathrin Heavy Chains, Dogs, Epithelial Cells, Golgi Apparatus, Humans, Inulin, Lysosomes, Protein Transport, Receptors, LDL, Receptors, Transferrin, Tight Junctions, Time Factors, trans-Golgi Network
Abstract

<p>Clathrin-coated vesicles are vehicles for intracellular trafficking in all nucleated cells, from yeasts to humans. Many studies have demonstrated their essential roles in endocytosis and cellular signalling processes at the plasma membrane. By contrast, very few of their non-endocytic trafficking roles are known, the best characterized being the transport of hydrolases from the Golgi complex to the lysosome. Here we show that clathrin is required for polarity of the basolateral plasma membrane proteins in the epithelial cell line MDCK. Clathrin knockdown depolarized most basolateral proteins, by interfering with their biosynthetic delivery and recycling, but did not affect the polarity of apical proteins. Quantitative live imaging showed that chronic and acute clathrin knockdown selectively slowed down the exit of basolateral proteins from the Golgi complex, and promoted their mis-sorting into apical carrier vesicles. Our results demonstrate a broad requirement for clathrin in basolateral protein trafficking in epithelial cells.</p>

DOI10.1038/nature06828
Alternate JournalNature
PubMed ID18401403
PubMed Central IDPMC4078870
Grant ListR01 EY008538 / EY / NEI NIH HHS / United States
R01 GM034107 / GM / NIGMS NIH HHS / United States

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