The volume-regulated anion channel is formed by LRRC8 heteromers – molecular identification and roles in membrane transport and physiology
Cellular volume regulation is fundamental for numerous physiological processes. The volume-regulated anion channel, VRAC, plays a crucial role in regulatory volume decrease. This channel, which is ubiquitously expressed in vertebrates, has been vastly characterized by electrophysiological means. It...
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Veröffentlicht in: | Biological chemistry 2015-09, Vol.396 (9), p.975-990 |
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description | Cellular volume regulation is fundamental for numerous physiological processes. The volume-regulated anion channel, VRAC, plays a crucial role in regulatory volume decrease. This channel, which is ubiquitously expressed in vertebrates, has been vastly characterized by electrophysiological means. It opens upon cell swelling and conducts chloride and arguably organic osmolytes. VRAC has been proposed to be critically involved in various cellular and organismal functions, including cell proliferation and migration, apoptosis, transepithelial transport, swelling-induced exocytosis and intercellular communication. It may also play a role in pathological states like cancer and ischemia. Despite many efforts, the molecular identity of VRAC had remained elusive for decades, until the recent discovery of heteromers of LRRC8A with other LRRC8 family members as an essential VRAC component. This identification marks a starting point for studies on the structure-function relation, for molecular biological investigations of its cell biology and for re-evaluating the physiological roles of VRAC. This review recapitulates the identification of LRRC8 heteromers as VRAC components, depicts the similarities between LRRC8 proteins and pannexins, and discussed whether VRAC conducts larger osmolytes. Furthermore, proposed physiological functions of VRAC and the present knowledge about the physiological significance of LRRC8 proteins are summarized and collated. |
doi_str_mv | 10.1515/hsz-2015-0127 |
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The volume-regulated anion channel, VRAC, plays a crucial role in regulatory volume decrease. This channel, which is ubiquitously expressed in vertebrates, has been vastly characterized by electrophysiological means. It opens upon cell swelling and conducts chloride and arguably organic osmolytes. VRAC has been proposed to be critically involved in various cellular and organismal functions, including cell proliferation and migration, apoptosis, transepithelial transport, swelling-induced exocytosis and intercellular communication. It may also play a role in pathological states like cancer and ischemia. Despite many efforts, the molecular identity of VRAC had remained elusive for decades, until the recent discovery of heteromers of LRRC8A with other LRRC8 family members as an essential VRAC component. This identification marks a starting point for studies on the structure-function relation, for molecular biological investigations of its cell biology and for re-evaluating the physiological roles of VRAC. This review recapitulates the identification of LRRC8 heteromers as VRAC components, depicts the similarities between LRRC8 proteins and pannexins, and discussed whether VRAC conducts larger osmolytes. Furthermore, proposed physiological functions of VRAC and the present knowledge about the physiological significance of LRRC8 proteins are summarized and collated.</description><identifier>ISSN: 1431-6730</identifier><identifier>EISSN: 1437-4315</identifier><identifier>DOI: 10.1515/hsz-2015-0127</identifier><identifier>PMID: 25868000</identifier><language>eng</language><publisher>Germany: De Gruyter</publisher><subject>Animals ; Anions ; Apoptosis ; Cell migration ; Cell proliferation ; Cell signaling ; Cell size ; Exocytosis ; Humans ; Ion channels ; Ion Channels - metabolism ; Ischemia ; leucine-rich repeat-containing ; Membrane Proteins - metabolism ; membrane transport ; Membrane Transport Proteins - metabolism ; Molecular structure ; osmotic swelling ; Physiology ; Proteins ; regulatory volume decrease (RVD) ; Structure-function relationships ; Swelling ; Transport ; Vertebrates ; volume-sensitive organic osmolyte/anion channel (VSOAC)</subject><ispartof>Biological chemistry, 2015-09, Vol.396 (9), p.975-990</ispartof><rights>2015 by De Gruyter</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-c629f147643844f04e3148ef2a44f1d037dbfdc3d28b771f3301a19fba11c6013</citedby><cites>FETCH-LOGICAL-c443t-c629f147643844f04e3148ef2a44f1d037dbfdc3d28b771f3301a19fba11c6013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/hsz-2015-0127/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/hsz-2015-0127/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,66754,68538</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25868000$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stauber, Tobias</creatorcontrib><title>The volume-regulated anion channel is formed by LRRC8 heteromers – molecular identification and roles in membrane transport and physiology</title><title>Biological chemistry</title><addtitle>Biol Chem</addtitle><description>Cellular volume regulation is fundamental for numerous physiological processes. The volume-regulated anion channel, VRAC, plays a crucial role in regulatory volume decrease. This channel, which is ubiquitously expressed in vertebrates, has been vastly characterized by electrophysiological means. It opens upon cell swelling and conducts chloride and arguably organic osmolytes. VRAC has been proposed to be critically involved in various cellular and organismal functions, including cell proliferation and migration, apoptosis, transepithelial transport, swelling-induced exocytosis and intercellular communication. It may also play a role in pathological states like cancer and ischemia. Despite many efforts, the molecular identity of VRAC had remained elusive for decades, until the recent discovery of heteromers of LRRC8A with other LRRC8 family members as an essential VRAC component. This identification marks a starting point for studies on the structure-function relation, for molecular biological investigations of its cell biology and for re-evaluating the physiological roles of VRAC. This review recapitulates the identification of LRRC8 heteromers as VRAC components, depicts the similarities between LRRC8 proteins and pannexins, and discussed whether VRAC conducts larger osmolytes. Furthermore, proposed physiological functions of VRAC and the present knowledge about the physiological significance of LRRC8 proteins are summarized and collated.</description><subject>Animals</subject><subject>Anions</subject><subject>Apoptosis</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Cell signaling</subject><subject>Cell size</subject><subject>Exocytosis</subject><subject>Humans</subject><subject>Ion channels</subject><subject>Ion Channels - metabolism</subject><subject>Ischemia</subject><subject>leucine-rich repeat-containing</subject><subject>Membrane Proteins - metabolism</subject><subject>membrane transport</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Molecular structure</subject><subject>osmotic swelling</subject><subject>Physiology</subject><subject>Proteins</subject><subject>regulatory volume decrease (RVD)</subject><subject>Structure-function relationships</subject><subject>Swelling</subject><subject>Transport</subject><subject>Vertebrates</subject><subject>volume-sensitive organic osmolyte/anion channel (VSOAC)</subject><issn>1431-6730</issn><issn>1437-4315</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc9u1DAQxiNERUvhyBVZ4sLF1GM7cXJCaMU_aaVKVTlHTjLeuHLsxU5A4cQDcOMNeRK83VIkxMWe8fzm82i-ongG7BWUUF6M6RvlDErKgKsHxRlIoagUUD68jYFWSrDT4nFKN4yxmknxqDjlZV3VOT0rflyPSL4Et0xII-4Wp2cciPY2eNKP2nt0xCZiQpzye7eS7dXVpiYjzhjDhDGRX99_kik47HNvJHZAP1tjez0fJLQfSMzFRKwnE05d1B7JnM-0D3G-re_HNdngwm59UpwY7RI-vbvPi0_v3l5vPtDt5fuPmzdb2kspZtpXvDEgVSVFLaVhEgXIGg3XOYOBCTV0ZujFwOtOKTBCMNDQmE4D9BUDcV68POruY_i8YJrbyaYencvDhSW1oABKWTHOM_riH_QmLNHn6Vou6qbkioHKFD1SfQwpRTTtPtpJx7UF1h5sarNN7cGm9mBT5p_fqS5d3us9_ceXDLw-Al-1y5secBeXNQd_f_-_cFM1udKoUvwG7YikRw</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Stauber, Tobias</creator><general>De Gruyter</general><general>Walter de Gruyter GmbH</general><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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20150901</creationdate><title>The volume-regulated anion channel is formed by LRRC8 heteromers – molecular identification and roles in membrane transport and physiology</title><author>Stauber, Tobias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-c629f147643844f04e3148ef2a44f1d037dbfdc3d28b771f3301a19fba11c6013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Anions</topic><topic>Apoptosis</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Cell signaling</topic><topic>Cell size</topic><topic>Exocytosis</topic><topic>Humans</topic><topic>Ion channels</topic><topic>Ion Channels - metabolism</topic><topic>Ischemia</topic><topic>leucine-rich repeat-containing</topic><topic>Membrane Proteins - metabolism</topic><topic>membrane transport</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Molecular structure</topic><topic>osmotic swelling</topic><topic>Physiology</topic><topic>Proteins</topic><topic>regulatory volume decrease (RVD)</topic><topic>Structure-function relationships</topic><topic>Swelling</topic><topic>Transport</topic><topic>Vertebrates</topic><topic>volume-sensitive organic osmolyte/anion channel (VSOAC)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stauber, Tobias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stauber, Tobias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The volume-regulated anion channel is formed by LRRC8 heteromers – molecular identification and roles in membrane transport and physiology</atitle><jtitle>Biological chemistry</jtitle><addtitle>Biol Chem</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>396</volume><issue>9</issue><spage>975</spage><epage>990</epage><pages>975-990</pages><issn>1431-6730</issn><eissn>1437-4315</eissn><abstract>Cellular volume regulation is fundamental for numerous physiological processes. The volume-regulated anion channel, VRAC, plays a crucial role in regulatory volume decrease. This channel, which is ubiquitously expressed in vertebrates, has been vastly characterized by electrophysiological means. It opens upon cell swelling and conducts chloride and arguably organic osmolytes. VRAC has been proposed to be critically involved in various cellular and organismal functions, including cell proliferation and migration, apoptosis, transepithelial transport, swelling-induced exocytosis and intercellular communication. It may also play a role in pathological states like cancer and ischemia. Despite many efforts, the molecular identity of VRAC had remained elusive for decades, until the recent discovery of heteromers of LRRC8A with other LRRC8 family members as an essential VRAC component. This identification marks a starting point for studies on the structure-function relation, for molecular biological investigations of its cell biology and for re-evaluating the physiological roles of VRAC. This review recapitulates the identification of LRRC8 heteromers as VRAC components, depicts the similarities between LRRC8 proteins and pannexins, and discussed whether VRAC conducts larger osmolytes. Furthermore, proposed physiological functions of VRAC and the present knowledge about the physiological significance of LRRC8 proteins are summarized and collated.</abstract><cop>Germany</cop><pub>De Gruyter</pub><pmid>25868000</pmid><doi>10.1515/hsz-2015-0127</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Anions Apoptosis Cell migration Cell proliferation Cell signaling Cell size Exocytosis Humans Ion channels Ion Channels - metabolism Ischemia leucine-rich repeat-containing Membrane Proteins - metabolism membrane transport Membrane Transport Proteins - metabolism Molecular structure osmotic swelling Physiology Proteins regulatory volume decrease (RVD) Structure-function relationships Swelling Transport Vertebrates volume-sensitive organic osmolyte/anion channel (VSOAC) |
title | The volume-regulated anion channel is formed by LRRC8 heteromers – molecular identification and roles in membrane transport and physiology |
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