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EXOCYST COMPLEX AND MEMBRANE TRAFFICKING IN POLARIZED EPITHELIAL CELLS

The octameric exocyst complex is associated with the junctional complex and recycling endosomes, and is proposed to selectively tether cargo vesicles directed toward the basolateral surface of polarized Madin-Darby canine kidney (MDCK) cells. I observed that the exocyst subunits Sec6, Sec8, and Exo70 were localized to early endosomes, transferrin-positive common recycling endosomes, and Rab11a-positive apical recycling endosomes of polarized MDCK cells. Consistent with its localization to multiple populations of endosomes, addition of function-blocking Sec8 antibodies to streptolysin-O permeabilized cells revealed exocyst requirements for several endocytic pathways including basolateral recycling, apical recycling, and basolateral-to-apical transcytosis. The latter was selectively dependent on interactions between the small GTPase Rab11a and Sec15A and was inhibited by the expression of the C-terminus of Sec15A or downregulation of Sec15A expression using shRNA. These results indicate that the exocyst complex may be a multi-purpose regulator of endocytic traffic directed toward both poles of polarized epithelial cells, and that transcytotic traffic is likely to require Rab11a-dependent recruitment and modulation of exocyst function, likely through interactions with Sec15A.

Identiferoai:union.ndltd.org:PITT/oai:PITTETD:etd-01222008-164016
Date14 February 2008
CreatorsOztan Matos, Asli
ContributorsMeir Aridor, Linton Traub, Ora Weisz, Gerard Apodaca, Adam Linstedt
PublisherUniversity of Pittsburgh
Source SetsUniversity of Pittsburgh
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.library.pitt.edu/ETD/available/etd-01222008-164016/
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