Caveolae and intracellular trafficking of cholesterol
被引:97
作者:
Fielding, CJ
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Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94193 USAUniv Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94193 USA
Fielding, CJ
[1
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Fielding, PE
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机构:Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94193 USA
Fielding, PE
机构:
[1] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94193 USA
[2] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94193 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94193 USA
Caveolae, free cholesterol (FC)-rich microdomains of the plasma membrane, are both a terminus for the intracellular transit of newly synthesized and recycling cellular FC, and a site for FC efflux to the extracellular medium. The same domains play key roles as locations for the assembly of signaling complexes and for the endocytosis of selected ligands. Caveolin, the major structural protein of caveolae, plays a regulatory role in growth, the cell cycle, and cell adhesion. Each of these functions is FC-dependent. Caveolae appear to act as both sensors and regulators of cellular FC content, and in this way mediate an array of membrane-dependent cell functions. (C) 2001 Elsevier Science BY All rights reserved.