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Assembly and Turnover of Caveolae: What Do We Really Know?

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2016.00068

Keywords

caveolae; caveolin-1; GFP; trafficking; degradation; breast cancer; pulmonary arterial hypertension; congenital generalized lipodystrophy

Funding

  1. NIH [R01 HL111259, R01 HL111259 01S1]
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL111259] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R25GM062459] Funding Source: NIH RePORTER

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In addition to containing highly dynamic nanoscale domains, the plasma membranes of many cell types are decorated with caveolae, flask shaped domains enriched in the structural protein caveolin-1 (Cav1). The importance of caveolae in numerous cellular functions and processes has become well-recognized, and recent years have seen dramatic advances in our understanding of how caveolae assemble and the mechanisms control the turnover of Cav1. At the same time, work from our lab and others have revealed that commonly utilized strategies such as overexpression and tagging of Cav1 have unexpectedly complex consequences on the trafficking and fate of Cav1. Here, we discuss the implications of these findings for current models of caveolae biogenesis and Cav1 turnover. In addition, we discuss how disease-associated mutants of Cav1 impact caveolae assembly and outline open questions in this still-emerging area.

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