EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress

Caveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localiz...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Current biology 2017-10, Vol.27 (19), p.2951-2962.e5
Hauptverfasser: Yeow, Ivana, Howard, Gillian, Chadwick, Jessica, Mendoza-Topaz, Carolina, Hansen, Carsten G., Nichols, Benjamin J., Shvets, Elena
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2962.e5
container_issue 19
container_start_page 2951
container_title Current biology
container_volume 27
creator Yeow, Ivana
Howard, Gillian
Chadwick, Jessica
Mendoza-Topaz, Carolina
Hansen, Carsten G.
Nichols, Benjamin J.
Shvets, Elena
description Caveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localize to the constricted neck. Here we make extensive use of multiple CRISPR/Cas9-generated gene knockout and knockin cell lines to investigate the role of Eps15 Homology Domain (EHD) proteins at the neck of caveolae. We show that EHD1, EHD2, and EHD4 are recruited to caveolae. Recruitment of the other EHDs increases markedly when EHD2, which has been previously detected at caveolae, is absent. Construction of knockout cell lines lacking EHDs 1, 2, and 4 confirms this apparent functional redundancy. Two striking sets of phenotypes are observed in EHD1,2,4 knockout cells: (1) the characteristic clustering of caveolae into higher-order assemblies is absent; and (2) when the EHD1,2,4 knockout cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma membrane is prone to rupture. Our data identify the first molecular components that act to cluster caveolae into a membrane ultrastructure with the potential to extend stretch-buffering capacity and support a revised model for the function of EHDs at the caveolar neck. •EHD1, 2, and 4 are all recruited to caveolae•EHD proteins promote the formation of clustered arrays of caveolae•EHD proteins are required for morphogenesis of caveolae under repeated stretch forces•Loss of EHD proteins increases stretch-induced damage to the plasma membrane Yeow et al. apply gene-editing approaches to show that members of the EHD protein family are recruited to plasma membrane invaginations termed caveolae. The EHD proteins act to promote clustering of caveolae into higher-order assemblies and also to protect the plasma membrane from rupture under stretch forces.
doi_str_mv 10.1016/j.cub.2017.07.047
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5640515</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S096098221730951X</els_id><sourcerecordid>1942711883</sourcerecordid><originalsourceid>FETCH-LOGICAL-c517t-f51de4a7b2dd2dc97b930c43ceda5aa73ea174b12f49d8d33dbceae7fa1253253</originalsourceid><addsrcrecordid>eNp9kVFrFDEUhYModm39Ab5IHn2ZNclkNjMIgkxrK7Qotn0Od5I7bZbZZE0yC_57s2xb7EvhhhvId84N9xDygbMlZ3z1eb0087AUjKslKyXVK7LgreoqJmXzmixYt2JV1wpxRN6ltGaMi7ZbvSVHpcmatd2ChLOLU_orhozOJ9qHsMUIGWkO9Bz94d7DDsMEkfbTnDLGRMHbPXEFzudyHgmkdo7O39HfuMWitPQKzT14Z2Ci1zliSifkzQhTwvcP_Zjcfj-76S-qy5_nP_pvl5VpuMrV2HCLEtQgrBXWdGroamZkbdBCA6BqBK7kwMUoO9vauraDQUA1AhdNXeqYfD34budhg9agzxEmvY1uA_GvDuD08xfv7vVd2OlmJVnD9wafHgxi-DNjynrjksFpAo9hTpp3UijO27YuKD-gJoaUIo5PYzjT-6D0Wpeg9D4ozUpJVTQf___fk-IxmQJ8OQBYtrRzGHUyDn1ZgItosrbBvWD_D9CMpuA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1942711883</pqid></control><display><type>article</type><title>EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Access via ScienceDirect (Elsevier)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Yeow, Ivana ; Howard, Gillian ; Chadwick, Jessica ; Mendoza-Topaz, Carolina ; Hansen, Carsten G. ; Nichols, Benjamin J. ; Shvets, Elena</creator><creatorcontrib>Yeow, Ivana ; Howard, Gillian ; Chadwick, Jessica ; Mendoza-Topaz, Carolina ; Hansen, Carsten G. ; Nichols, Benjamin J. ; Shvets, Elena</creatorcontrib><description>Caveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localize to the constricted neck. Here we make extensive use of multiple CRISPR/Cas9-generated gene knockout and knockin cell lines to investigate the role of Eps15 Homology Domain (EHD) proteins at the neck of caveolae. We show that EHD1, EHD2, and EHD4 are recruited to caveolae. Recruitment of the other EHDs increases markedly when EHD2, which has been previously detected at caveolae, is absent. Construction of knockout cell lines lacking EHDs 1, 2, and 4 confirms this apparent functional redundancy. Two striking sets of phenotypes are observed in EHD1,2,4 knockout cells: (1) the characteristic clustering of caveolae into higher-order assemblies is absent; and (2) when the EHD1,2,4 knockout cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma membrane is prone to rupture. Our data identify the first molecular components that act to cluster caveolae into a membrane ultrastructure with the potential to extend stretch-buffering capacity and support a revised model for the function of EHDs at the caveolar neck. •EHD1, 2, and 4 are all recruited to caveolae•EHD proteins promote the formation of clustered arrays of caveolae•EHD proteins are required for morphogenesis of caveolae under repeated stretch forces•Loss of EHD proteins increases stretch-induced damage to the plasma membrane Yeow et al. apply gene-editing approaches to show that members of the EHD protein family are recruited to plasma membrane invaginations termed caveolae. The EHD proteins act to promote clustering of caveolae into higher-order assemblies and also to protect the plasma membrane from rupture under stretch forces.</description><identifier>ISSN: 0960-9822</identifier><identifier>ISSN: 1879-0445</identifier><identifier>EISSN: 1879-0445</identifier><identifier>DOI: 10.1016/j.cub.2017.07.047</identifier><identifier>PMID: 28943089</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Biomechanical Phenomena ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; caveolae ; Caveolae - physiology ; caveolin ; cavin ; cell ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; EHD2 ; membrane ; Mice ; NIH 3T3 Cells ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Stress, Mechanical ; stretch ; Vesicular Transport Proteins - genetics ; Vesicular Transport Proteins - metabolism</subject><ispartof>Current biology, 2017-10, Vol.27 (19), p.2951-2962.e5</ispartof><rights>2017 MRC Laboratory of Molecular Biology</rights><rights>Copyright © 2017 MRC Laboratory of Molecular Biology. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2017 MRC Laboratory of Molecular Biology 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-f51de4a7b2dd2dc97b930c43ceda5aa73ea174b12f49d8d33dbceae7fa1253253</citedby><cites>FETCH-LOGICAL-c517t-f51de4a7b2dd2dc97b930c43ceda5aa73ea174b12f49d8d33dbceae7fa1253253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cub.2017.07.047$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28943089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yeow, Ivana</creatorcontrib><creatorcontrib>Howard, Gillian</creatorcontrib><creatorcontrib>Chadwick, Jessica</creatorcontrib><creatorcontrib>Mendoza-Topaz, Carolina</creatorcontrib><creatorcontrib>Hansen, Carsten G.</creatorcontrib><creatorcontrib>Nichols, Benjamin J.</creatorcontrib><creatorcontrib>Shvets, Elena</creatorcontrib><title>EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress</title><title>Current biology</title><addtitle>Curr Biol</addtitle><description>Caveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localize to the constricted neck. Here we make extensive use of multiple CRISPR/Cas9-generated gene knockout and knockin cell lines to investigate the role of Eps15 Homology Domain (EHD) proteins at the neck of caveolae. We show that EHD1, EHD2, and EHD4 are recruited to caveolae. Recruitment of the other EHDs increases markedly when EHD2, which has been previously detected at caveolae, is absent. Construction of knockout cell lines lacking EHDs 1, 2, and 4 confirms this apparent functional redundancy. Two striking sets of phenotypes are observed in EHD1,2,4 knockout cells: (1) the characteristic clustering of caveolae into higher-order assemblies is absent; and (2) when the EHD1,2,4 knockout cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma membrane is prone to rupture. Our data identify the first molecular components that act to cluster caveolae into a membrane ultrastructure with the potential to extend stretch-buffering capacity and support a revised model for the function of EHDs at the caveolar neck. •EHD1, 2, and 4 are all recruited to caveolae•EHD proteins promote the formation of clustered arrays of caveolae•EHD proteins are required for morphogenesis of caveolae under repeated stretch forces•Loss of EHD proteins increases stretch-induced damage to the plasma membrane Yeow et al. apply gene-editing approaches to show that members of the EHD protein family are recruited to plasma membrane invaginations termed caveolae. The EHD proteins act to promote clustering of caveolae into higher-order assemblies and also to protect the plasma membrane from rupture under stretch forces.</description><subject>Animals</subject><subject>Biomechanical Phenomena</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>caveolae</subject><subject>Caveolae - physiology</subject><subject>caveolin</subject><subject>cavin</subject><subject>cell</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>EHD2</subject><subject>membrane</subject><subject>Mice</subject><subject>NIH 3T3 Cells</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclear Proteins - metabolism</subject><subject>Stress, Mechanical</subject><subject>stretch</subject><subject>Vesicular Transport Proteins - genetics</subject><subject>Vesicular Transport Proteins - metabolism</subject><issn>0960-9822</issn><issn>1879-0445</issn><issn>1879-0445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kVFrFDEUhYModm39Ab5IHn2ZNclkNjMIgkxrK7Qotn0Od5I7bZbZZE0yC_57s2xb7EvhhhvId84N9xDygbMlZ3z1eb0087AUjKslKyXVK7LgreoqJmXzmixYt2JV1wpxRN6ltGaMi7ZbvSVHpcmatd2ChLOLU_orhozOJ9qHsMUIGWkO9Bz94d7DDsMEkfbTnDLGRMHbPXEFzudyHgmkdo7O39HfuMWitPQKzT14Z2Ci1zliSifkzQhTwvcP_Zjcfj-76S-qy5_nP_pvl5VpuMrV2HCLEtQgrBXWdGroamZkbdBCA6BqBK7kwMUoO9vauraDQUA1AhdNXeqYfD34budhg9agzxEmvY1uA_GvDuD08xfv7vVd2OlmJVnD9wafHgxi-DNjynrjksFpAo9hTpp3UijO27YuKD-gJoaUIo5PYzjT-6D0Wpeg9D4ozUpJVTQf___fk-IxmQJ8OQBYtrRzGHUyDn1ZgItosrbBvWD_D9CMpuA</recordid><startdate>20171009</startdate><enddate>20171009</enddate><creator>Yeow, Ivana</creator><creator>Howard, Gillian</creator><creator>Chadwick, Jessica</creator><creator>Mendoza-Topaz, Carolina</creator><creator>Hansen, Carsten G.</creator><creator>Nichols, Benjamin J.</creator><creator>Shvets, Elena</creator><general>Elsevier Ltd</general><general>Cell Press</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171009</creationdate><title>EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress</title><author>Yeow, Ivana ; Howard, Gillian ; Chadwick, Jessica ; Mendoza-Topaz, Carolina ; Hansen, Carsten G. ; Nichols, Benjamin J. ; Shvets, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-f51de4a7b2dd2dc97b930c43ceda5aa73ea174b12f49d8d33dbceae7fa1253253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Biomechanical Phenomena</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>caveolae</topic><topic>Caveolae - physiology</topic><topic>caveolin</topic><topic>cavin</topic><topic>cell</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>EHD2</topic><topic>membrane</topic><topic>Mice</topic><topic>NIH 3T3 Cells</topic><topic>Nuclear Proteins - genetics</topic><topic>Nuclear Proteins - metabolism</topic><topic>Stress, Mechanical</topic><topic>stretch</topic><topic>Vesicular Transport Proteins - genetics</topic><topic>Vesicular Transport Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeow, Ivana</creatorcontrib><creatorcontrib>Howard, Gillian</creatorcontrib><creatorcontrib>Chadwick, Jessica</creatorcontrib><creatorcontrib>Mendoza-Topaz, Carolina</creatorcontrib><creatorcontrib>Hansen, Carsten G.</creatorcontrib><creatorcontrib>Nichols, Benjamin J.</creatorcontrib><creatorcontrib>Shvets, Elena</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeow, Ivana</au><au>Howard, Gillian</au><au>Chadwick, Jessica</au><au>Mendoza-Topaz, Carolina</au><au>Hansen, Carsten G.</au><au>Nichols, Benjamin J.</au><au>Shvets, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress</atitle><jtitle>Current biology</jtitle><addtitle>Curr Biol</addtitle><date>2017-10-09</date><risdate>2017</risdate><volume>27</volume><issue>19</issue><spage>2951</spage><epage>2962.e5</epage><pages>2951-2962.e5</pages><issn>0960-9822</issn><issn>1879-0445</issn><eissn>1879-0445</eissn><abstract>Caveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localize to the constricted neck. Here we make extensive use of multiple CRISPR/Cas9-generated gene knockout and knockin cell lines to investigate the role of Eps15 Homology Domain (EHD) proteins at the neck of caveolae. We show that EHD1, EHD2, and EHD4 are recruited to caveolae. Recruitment of the other EHDs increases markedly when EHD2, which has been previously detected at caveolae, is absent. Construction of knockout cell lines lacking EHDs 1, 2, and 4 confirms this apparent functional redundancy. Two striking sets of phenotypes are observed in EHD1,2,4 knockout cells: (1) the characteristic clustering of caveolae into higher-order assemblies is absent; and (2) when the EHD1,2,4 knockout cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma membrane is prone to rupture. Our data identify the first molecular components that act to cluster caveolae into a membrane ultrastructure with the potential to extend stretch-buffering capacity and support a revised model for the function of EHDs at the caveolar neck. •EHD1, 2, and 4 are all recruited to caveolae•EHD proteins promote the formation of clustered arrays of caveolae•EHD proteins are required for morphogenesis of caveolae under repeated stretch forces•Loss of EHD proteins increases stretch-induced damage to the plasma membrane Yeow et al. apply gene-editing approaches to show that members of the EHD protein family are recruited to plasma membrane invaginations termed caveolae. The EHD proteins act to promote clustering of caveolae into higher-order assemblies and also to protect the plasma membrane from rupture under stretch forces.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28943089</pmid><doi>10.1016/j.cub.2017.07.047</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0960-9822
ispartof Current biology, 2017-10, Vol.27 (19), p.2951-2962.e5
issn 0960-9822
1879-0445
1879-0445
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5640515
source MEDLINE; Cell Press Free Archives; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals
subjects Animals
Biomechanical Phenomena
Carrier Proteins - genetics
Carrier Proteins - metabolism
caveolae
Caveolae - physiology
caveolin
cavin
cell
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
EHD2
membrane
Mice
NIH 3T3 Cells
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Stress, Mechanical
stretch
Vesicular Transport Proteins - genetics
Vesicular Transport Proteins - metabolism
title EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T20%3A43%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EHD%20Proteins%20Cooperate%20to%20Generate%20Caveolar%20Clusters%20and%20to%20Maintain%20Caveolae%20during%20Repeated%20Mechanical%20Stress&rft.jtitle=Current%20biology&rft.au=Yeow,%20Ivana&rft.date=2017-10-09&rft.volume=27&rft.issue=19&rft.spage=2951&rft.epage=2962.e5&rft.pages=2951-2962.e5&rft.issn=0960-9822&rft.eissn=1879-0445&rft_id=info:doi/10.1016/j.cub.2017.07.047&rft_dat=%3Cproquest_pubme%3E1942711883%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1942711883&rft_id=info:pmid/28943089&rft_els_id=S096098221730951X&rfr_iscdi=true