Selective Roles for Cholesterol and Actin in Compartmentalization of Different Proteins in the Golgi and Plasma Membrane of Polarized CellsS
To determine the roles of cholesterol and the actin cytoskeleton in apical and basolateral protein organization and sorting, we have performed comprehensive confocal fluorescence recovery after photobleaching analyses of apical and basolateral and raft- and non-raft-associated proteins, both at the...
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Published in | The Journal of biological chemistry Vol. 283; no. 43; pp. 29545 - 29553 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
American Society for Biochemistry and Molecular Biology
24.10.2008
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Subjects | |
Online Access | Get full text |
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Summary: | To determine the roles of cholesterol and the actin cytoskeleton in apical
and basolateral protein organization and sorting, we have performed
comprehensive confocal fluorescence recovery after photobleaching analyses of
apical and basolateral and raft- and non-raft-associated proteins, both at the
plasma membrane and in the Golgi apparatus of polarized MDCK cells. We show
that at both the apical and basolateral plasma membrane domains,
raft-associated proteins diffuse faster than non-raft-associated proteins and
that, different from the latter, they become restricted upon depletion of
cholesterol. Furthermore, only transmembrane apical proteins are restricted by
the actin network. This indicates that cholesterol-dependent domains exist
both at the apical and basolateral membranes of polarized cells and that the
actin cytoskeleton has a predominant role in the organization of transmembrane
proteins independent of their association with rafts at the apical membrane.
In the Golgi apparatus apical proteins appear to be segregated from the
basolateral ones in a compartment that is sensitive both to cholesterol
depletion and actin rearrangements. Furthermore, consistent with the role of
actin rearrangements in apical protein sorting, we found that apical proteins
exhibit a differential sensitivity to actin depolymerization in the Golgi of
polarized and nonpolarized cells. |
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Bibliography: | To whom correspondence should be addressed: Unité de Trafic Membranaire et Pathogénèse, Institut Pasteur, 25 rue du Docteur Roux, 75015 Paris, France. Tel.: 33-1-45688277; Fax: 33-1-40613238; E-mail: zurzolo@pasteur.fr, zurzolo@unina.it. This work was supported by Agence Nationale de la Recherche Grant 05-BLAN 296-01 and Ministero dell' Università e della Ricerca Scientifica e Tecnologica Grant PRIN 2006. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. The on-line version of this article (available at http://www.jbc.org) contains supplemental Figs. S1-S4. |
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M803819200 |