<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-18T00:15:40Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/124628" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/124628</identifier><datestamp>2025-12-04T21:14:20Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478781</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Cholesterol depletion in adipocytes causes caveolae collapse concomitant with proteosomal degradation of cavin-2 in a switch-like fashion</dc:title>
   <dc:creator>Breen, Michael P., 1940-</dc:creator>
   <dc:creator>Camps Camprubí, Marta</dc:creator>
   <dc:creator>Carvalho-Simoes, Francisco</dc:creator>
   <dc:creator>Zorzano Olarte, Antonio</dc:creator>
   <dc:creator>Pilch, Paul F.</dc:creator>
   <dc:subject>Colesterol</dc:subject>
   <dc:subject>Proteïnes de membrana</dc:subject>
   <dc:subject>Cèl·lules animals</dc:subject>
   <dc:subject>Cholesterol</dc:subject>
   <dc:subject>Membrane proteins</dc:subject>
   <dc:subject>Animal cells</dc:subject>
   <dc:description>Caveolae, little caves of cell surfaces, are enriched in cholesterol, a certain level of which is required for their structural integrity. Here we show in adipocytes that cavin-2, a peripheral membrane protein and one of 3 cavin isoforms present in caveolae from non-muscle tissue, is degraded upon cholesterol depletion in a rapid fashion resulting in collapse of caveolae. We exposed 3T3-L1 adipocytes to the cholesterol depleting agent methyl-β-cyclodextrin, which results in a sudden and extensive degradation of cavin-2 by the proteasome and a concomitant movement of cavin-1 from the plasma membrane to the cytosol along with loss of caveolae. The recovery of cavin-2 at the plasma membrane is cholesterol-dependent and is required for the return of cavin-1 from the cytosol to the cell surface and caveolae restoration. Expression of shRNA directed against cavin-2 also results in a cytosolic distribution of cavin-1 and loss of caveolae. Taken together, these data demonstrate that cavin-2 functions as a cholesterol responsive component of caveolae that is required for cavin-1 localization to the plasma membrane, and caveolae structural integrity.</dc:description>
   <dc:date>2018-09-17T13:11:26Z</dc:date>
   <dc:date>2018-09-17T13:11:26Z</dc:date>
   <dc:date>2012-04-06</dc:date>
   <dc:date>2018-09-17T13:11:26Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>1932-6203</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/124628</dc:identifier>
   <dc:identifier>639335</dc:identifier>
   <dc:identifier>22493697</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0034516</dc:relation>
   <dc:relation>PLoS One, 2012, vol. 7, num. 4, p. 1-8</dc:relation>
   <dc:relation>https://doi.org/10.1371/journal.pone.0034516</dc:relation>
   <dc:rights>cc-by (c) Breen, Michael P., 1940- et al., 2012</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>8 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Public Library of Science (PLoS)</dc:publisher>
   <dc:source>Articles publicats en revistes (Bioquímica i Biomedicina Molecular)</dc:source>
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