Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea
Stria vascularis of the mammalian cochlea transports K+ to establish the electrochemical property in the endolymph crucial for hearing. This epithelial tissue also transports various small molecules. To clarify the profile of proteins participating in the transport system in the stria vascularis, me...
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Veröffentlicht in: | The European journal of neuroscience 2015-08, Vol.42 (3), p.1984-2002 |
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container_title | The European journal of neuroscience |
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creator | Uetsuka, Satoru Ogata, Genki Nagamori, Shushi Isozumi, Noriyoshi Nin, Fumiaki Yoshida, Takamasa Komune, Shizuo Kitahara, Tadashi Kikkawa, Yoshiaki Inohara, Hidenori Kanai, Yoshikatsu Hibino, Hiroshi |
description | Stria vascularis of the mammalian cochlea transports K+ to establish the electrochemical property in the endolymph crucial for hearing. This epithelial tissue also transports various small molecules. To clarify the profile of proteins participating in the transport system in the stria vascularis, membrane components purified from the stria of adult rats were analysed by liquid chromatography tandem mass spectrometry. Of the 3236 proteins detected in the analysis, 1807 were membrane proteins. Ingenuity Knowledge Base and literature data identified 513 proteins as being expressed on the ‘plasma membrane’, these included 25 ion channels and 79 transporters. Sixteen of the former and 62 of the latter had not yet been identified in the stria. Unexpectedly, many Cl− and Ca2+ transport systems were found, suggesting that the dynamics of these ions play multiple roles. Several transporters for organic substances were also detected. Network analysis demonstrated that a few kinases, including protein kinase A, and Ca2+ were key regulators for the strial transports. In the library of channels and transporters, 19 new candidates for uncloned deafness‐related genes were identified. These resources provide a platform for understanding the molecular mechanisms underlying the epithelial transport essential for cochlear function and the pathophysiological processes involved in hearing disorders.
The membrane transport system in the cochlear stria vascularis is crucial for hearing. To elucidate the underlying molecular architecture, we conducted mass spectrometry of the stria; of 513 plasma membrane proteins, 16 channels and 62 transporters had not yet been identified in this tissue. Because the library contained 19 new candidates for uncloned deafness‐related genes, the resources we provide here are also useful to clarify the pathophysiological processes of deafness. |
doi_str_mv | 10.1111/ejn.12973 |
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The membrane transport system in the cochlear stria vascularis is crucial for hearing. To elucidate the underlying molecular architecture, we conducted mass spectrometry of the stria; of 513 plasma membrane proteins, 16 channels and 62 transporters had not yet been identified in this tissue. Because the library contained 19 new candidates for uncloned deafness‐related genes, the resources we provide here are also useful to clarify the pathophysiological processes of deafness.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1111/ejn.12973</identifier><identifier>PMID: 26060893</identifier><language>eng</language><publisher>France: Blackwell Publishing Ltd</publisher><subject>Animals ; Databases, Genetic ; Deafness - genetics ; Deafness - physiopathology ; Humans ; ion channel ; Male ; mass spectrometry ; Membrane Transport Proteins - genetics ; Membrane Transport Proteins - metabolism ; Mice ; Molecular Sequence Data ; Proteomics ; rat ; Rats ; Stria Vascularis - metabolism ; transporter</subject><ispartof>The European journal of neuroscience, 2015-08, Vol.42 (3), p.1984-2002</ispartof><rights>2015 Federation of European Neuroscience Societies and John Wiley & Sons Ltd</rights><rights>2015 Federation of European Neuroscience Societies and John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5833-4a20e66f8f4d87f334c3a016c81888ab50d7073591524da919066ead472ab5ec3</citedby><cites>FETCH-LOGICAL-c5833-4a20e66f8f4d87f334c3a016c81888ab50d7073591524da919066ead472ab5ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fejn.12973$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fejn.12973$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26060893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uetsuka, Satoru</creatorcontrib><creatorcontrib>Ogata, Genki</creatorcontrib><creatorcontrib>Nagamori, Shushi</creatorcontrib><creatorcontrib>Isozumi, Noriyoshi</creatorcontrib><creatorcontrib>Nin, Fumiaki</creatorcontrib><creatorcontrib>Yoshida, Takamasa</creatorcontrib><creatorcontrib>Komune, Shizuo</creatorcontrib><creatorcontrib>Kitahara, Tadashi</creatorcontrib><creatorcontrib>Kikkawa, Yoshiaki</creatorcontrib><creatorcontrib>Inohara, Hidenori</creatorcontrib><creatorcontrib>Kanai, Yoshikatsu</creatorcontrib><creatorcontrib>Hibino, Hiroshi</creatorcontrib><title>Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Stria vascularis of the mammalian cochlea transports K+ to establish the electrochemical property in the endolymph crucial for hearing. This epithelial tissue also transports various small molecules. To clarify the profile of proteins participating in the transport system in the stria vascularis, membrane components purified from the stria of adult rats were analysed by liquid chromatography tandem mass spectrometry. Of the 3236 proteins detected in the analysis, 1807 were membrane proteins. Ingenuity Knowledge Base and literature data identified 513 proteins as being expressed on the ‘plasma membrane’, these included 25 ion channels and 79 transporters. Sixteen of the former and 62 of the latter had not yet been identified in the stria. Unexpectedly, many Cl− and Ca2+ transport systems were found, suggesting that the dynamics of these ions play multiple roles. Several transporters for organic substances were also detected. Network analysis demonstrated that a few kinases, including protein kinase A, and Ca2+ were key regulators for the strial transports. In the library of channels and transporters, 19 new candidates for uncloned deafness‐related genes were identified. These resources provide a platform for understanding the molecular mechanisms underlying the epithelial transport essential for cochlear function and the pathophysiological processes involved in hearing disorders.
The membrane transport system in the cochlear stria vascularis is crucial for hearing. To elucidate the underlying molecular architecture, we conducted mass spectrometry of the stria; of 513 plasma membrane proteins, 16 channels and 62 transporters had not yet been identified in this tissue. Because the library contained 19 new candidates for uncloned deafness‐related genes, the resources we provide here are also useful to clarify the pathophysiological processes of deafness.</description><subject>Animals</subject><subject>Databases, Genetic</subject><subject>Deafness - genetics</subject><subject>Deafness - physiopathology</subject><subject>Humans</subject><subject>ion channel</subject><subject>Male</subject><subject>mass spectrometry</subject><subject>Membrane Transport Proteins - genetics</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Proteomics</subject><subject>rat</subject><subject>Rats</subject><subject>Stria Vascularis - metabolism</subject><subject>transporter</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhi1ERZeFA38A-QgSae04dpwj6idoWy583SyvMyEudrzYDmV_Bv8Yt9vtjZE8I9nPvCPPi9ArSo5oiWO4mY5o3bXsCVrQRpCq40I-RQvScVZJKr4foucp3RBCpGj4M3RYCyKI7NgC_b0KDszsdMQ6mtFmMHmOgMOA8wg45Wg1_q3TPWIT9uDXUU-Ac8lpE2LGaZsy-Hf4drRmxIWBlGDKVjs8hIg34zbZ4MIPa-5u5slkG6a0n-C199pZPWETzOhAv0AHg3YJXj7UJfpyfvb55LJafbr4cPJ-VRkuGasaXRMQYpBD08t2YKwxTBMqjKRSSr3mpG9Jy3hHed30uqMdEQJ037R1eQTDlujNTncTw68ZUlbeJgPOld-FOSna1pRx1pWzRG93qIkhpQiD2kTrddwqStSdA6o4oO4dKOzrB9l57aF_JPcrL8DxDri1Drb_V1JnH6_3ktWuw5ZF_3ns0PGnEi1rufp2faHk18tzvjql6pT9AwX-ogo</recordid><startdate>201508</startdate><enddate>201508</enddate><creator>Uetsuka, Satoru</creator><creator>Ogata, Genki</creator><creator>Nagamori, Shushi</creator><creator>Isozumi, Noriyoshi</creator><creator>Nin, Fumiaki</creator><creator>Yoshida, Takamasa</creator><creator>Komune, Shizuo</creator><creator>Kitahara, Tadashi</creator><creator>Kikkawa, Yoshiaki</creator><creator>Inohara, Hidenori</creator><creator>Kanai, Yoshikatsu</creator><creator>Hibino, Hiroshi</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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></search><sort><creationdate>201508</creationdate><title>Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea</title><author>Uetsuka, Satoru ; Ogata, Genki ; Nagamori, Shushi ; Isozumi, Noriyoshi ; Nin, Fumiaki ; Yoshida, Takamasa ; Komune, Shizuo ; Kitahara, Tadashi ; Kikkawa, Yoshiaki ; Inohara, Hidenori ; Kanai, Yoshikatsu ; Hibino, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5833-4a20e66f8f4d87f334c3a016c81888ab50d7073591524da919066ead472ab5ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Databases, Genetic</topic><topic>Deafness - genetics</topic><topic>Deafness - physiopathology</topic><topic>Humans</topic><topic>ion channel</topic><topic>Male</topic><topic>mass spectrometry</topic><topic>Membrane Transport Proteins - genetics</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Proteomics</topic><topic>rat</topic><topic>Rats</topic><topic>Stria Vascularis - metabolism</topic><topic>transporter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uetsuka, Satoru</creatorcontrib><creatorcontrib>Ogata, Genki</creatorcontrib><creatorcontrib>Nagamori, Shushi</creatorcontrib><creatorcontrib>Isozumi, Noriyoshi</creatorcontrib><creatorcontrib>Nin, Fumiaki</creatorcontrib><creatorcontrib>Yoshida, Takamasa</creatorcontrib><creatorcontrib>Komune, Shizuo</creatorcontrib><creatorcontrib>Kitahara, Tadashi</creatorcontrib><creatorcontrib>Kikkawa, Yoshiaki</creatorcontrib><creatorcontrib>Inohara, Hidenori</creatorcontrib><creatorcontrib>Kanai, Yoshikatsu</creatorcontrib><creatorcontrib>Hibino, Hiroshi</creatorcontrib><collection>Istex</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><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uetsuka, Satoru</au><au>Ogata, Genki</au><au>Nagamori, Shushi</au><au>Isozumi, Noriyoshi</au><au>Nin, Fumiaki</au><au>Yoshida, Takamasa</au><au>Komune, Shizuo</au><au>Kitahara, Tadashi</au><au>Kikkawa, Yoshiaki</au><au>Inohara, Hidenori</au><au>Kanai, Yoshikatsu</au><au>Hibino, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2015-08</date><risdate>2015</risdate><volume>42</volume><issue>3</issue><spage>1984</spage><epage>2002</epage><pages>1984-2002</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Stria vascularis of the mammalian cochlea transports K+ to establish the electrochemical property in the endolymph crucial for hearing. This epithelial tissue also transports various small molecules. To clarify the profile of proteins participating in the transport system in the stria vascularis, membrane components purified from the stria of adult rats were analysed by liquid chromatography tandem mass spectrometry. Of the 3236 proteins detected in the analysis, 1807 were membrane proteins. Ingenuity Knowledge Base and literature data identified 513 proteins as being expressed on the ‘plasma membrane’, these included 25 ion channels and 79 transporters. Sixteen of the former and 62 of the latter had not yet been identified in the stria. Unexpectedly, many Cl− and Ca2+ transport systems were found, suggesting that the dynamics of these ions play multiple roles. Several transporters for organic substances were also detected. Network analysis demonstrated that a few kinases, including protein kinase A, and Ca2+ were key regulators for the strial transports. In the library of channels and transporters, 19 new candidates for uncloned deafness‐related genes were identified. These resources provide a platform for understanding the molecular mechanisms underlying the epithelial transport essential for cochlear function and the pathophysiological processes involved in hearing disorders.
The membrane transport system in the cochlear stria vascularis is crucial for hearing. To elucidate the underlying molecular architecture, we conducted mass spectrometry of the stria; of 513 plasma membrane proteins, 16 channels and 62 transporters had not yet been identified in this tissue. Because the library contained 19 new candidates for uncloned deafness‐related genes, the resources we provide here are also useful to clarify the pathophysiological processes of deafness.</abstract><cop>France</cop><pub>Blackwell Publishing Ltd</pub><pmid>26060893</pmid><doi>10.1111/ejn.12973</doi><tpages>19</tpages></addata></record> |
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subjects | Animals Databases, Genetic Deafness - genetics Deafness - physiopathology Humans ion channel Male mass spectrometry Membrane Transport Proteins - genetics Membrane Transport Proteins - metabolism Mice Molecular Sequence Data Proteomics rat Rats Stria Vascularis - metabolism transporter |
title | Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea |
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