Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells
ATP-sensitive potassium channels (KATP channels) are critical nutrient sensors in many mammalian tissues. In the pancreas, KATP channels are essential for coupling glucose metabolism to insulin secretion. While orthologous genes for many components of metabolism–secretion coupling in mammals are pre...
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Veröffentlicht in: | Royal Society open science 2017-02, Vol.4 (2), p.160808-160808 |
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creator | Emfinger, Christopher H. Welscher, Alecia Yan, Zihan Wang, Yixi Conway, Hannah Moss, Jennifer B. Moss, Larry G. Remedi, Maria S. Nichols, Colin G. |
description | ATP-sensitive potassium channels (KATP channels) are critical nutrient sensors in many mammalian tissues. In the pancreas, KATP channels are essential for coupling glucose metabolism to insulin secretion. While orthologous genes for many components of metabolism–secretion coupling in mammals are present in lower vertebrates, their expression, functionality and ultimate impact on body glucose homeostasis are unclear. In this paper, we demonstrate that zebrafish islet β-cells express functional KATP channels of similar subunit composition, structure and metabolic sensitivity to their mammalian counterparts. We further show that pharmacological activation of native zebrafish KATP using diazoxide, a specific KATP channel opener, is sufficient to disturb glucose tolerance in adult zebrafish. That β-cell KATP channel expression and function are conserved between zebrafish and mammals illustrates the evolutionary conservation of islet metabolic sensing from fish to humans, and lends relevance to the use of zebrafish to model islet glucose sensing and diseases of membrane excitability such as neonatal diabetes. |
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In the pancreas, KATP channels are essential for coupling glucose metabolism to insulin secretion. While orthologous genes for many components of metabolism–secretion coupling in mammals are present in lower vertebrates, their expression, functionality and ultimate impact on body glucose homeostasis are unclear. In this paper, we demonstrate that zebrafish islet β-cells express functional KATP channels of similar subunit composition, structure and metabolic sensitivity to their mammalian counterparts. We further show that pharmacological activation of native zebrafish KATP using diazoxide, a specific KATP channel opener, is sufficient to disturb glucose tolerance in adult zebrafish. That β-cell KATP channel expression and function are conserved between zebrafish and mammals illustrates the evolutionary conservation of islet metabolic sensing from fish to humans, and lends relevance to the use of zebrafish to model islet glucose sensing and diseases of membrane excitability such as neonatal diabetes.</description><identifier>ISSN: 2054-5703</identifier><identifier>EISSN: 2054-5703</identifier><identifier>DOI: 10.1098/rsos.160808</identifier><identifier>PMID: 28386438</identifier><language>eng</language><publisher>England: The Royal Society Publishing</publisher><subject>Biochemistry And Biophysics ; Ion Channels ; katp ; Metabolism ; Pancreas ; Zebrafish</subject><ispartof>Royal Society open science, 2017-02, Vol.4 (2), p.160808-160808</ispartof><rights>2017 The Authors.</rights><rights>2017 The Authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-72a8ac39e2c0d2eb6d4ed319b4627df34ae4a23a93f0ed3aef322108e594a2583</citedby><cites>FETCH-LOGICAL-c572t-72a8ac39e2c0d2eb6d4ed319b4627df34ae4a23a93f0ed3aef322108e594a2583</cites><orcidid>0000-0002-4929-2134</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367309/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367309/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,2098,3311,27130,27907,27908,53774,53776,55538,55548</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28386438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Emfinger, Christopher H.</creatorcontrib><creatorcontrib>Welscher, Alecia</creatorcontrib><creatorcontrib>Yan, Zihan</creatorcontrib><creatorcontrib>Wang, Yixi</creatorcontrib><creatorcontrib>Conway, Hannah</creatorcontrib><creatorcontrib>Moss, Jennifer B.</creatorcontrib><creatorcontrib>Moss, Larry G.</creatorcontrib><creatorcontrib>Remedi, Maria S.</creatorcontrib><creatorcontrib>Nichols, Colin G.</creatorcontrib><title>Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells</title><title>Royal Society open science</title><addtitle>R. Soc. open sci</addtitle><addtitle>R Soc Open Sci</addtitle><description>ATP-sensitive potassium channels (KATP channels) are critical nutrient sensors in many mammalian tissues. In the pancreas, KATP channels are essential for coupling glucose metabolism to insulin secretion. While orthologous genes for many components of metabolism–secretion coupling in mammals are present in lower vertebrates, their expression, functionality and ultimate impact on body glucose homeostasis are unclear. In this paper, we demonstrate that zebrafish islet β-cells express functional KATP channels of similar subunit composition, structure and metabolic sensitivity to their mammalian counterparts. We further show that pharmacological activation of native zebrafish KATP using diazoxide, a specific KATP channel opener, is sufficient to disturb glucose tolerance in adult zebrafish. That β-cell KATP channel expression and function are conserved between zebrafish and mammals illustrates the evolutionary conservation of islet metabolic sensing from fish to humans, and lends relevance to the use of zebrafish to model islet glucose sensing and diseases of membrane excitability such as neonatal diabetes.</description><subject>Biochemistry And Biophysics</subject><subject>Ion Channels</subject><subject>katp</subject><subject>Metabolism</subject><subject>Pancreas</subject><subject>Zebrafish</subject><issn>2054-5703</issn><issn>2054-5703</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kU1LHTEUhofSUsW66r7MslDG5nMm2RRE1AqCpSouugiZzIk3l7nJNJkRrz-rP6S_qbkdK9dSusr5eHnek3OK4i1GBxhJ8TGmkA5wjQQSL4pdgjireIPoy614p9hPaYkQwhzRpm5eFztEUFEzKnaLm-P7IUJKLvhS-660kzfjJgm2PLz6UnUwgO_Aj-UQRp1106o0C-099Kl0vnyANmrr0qJ0qYex_PmjMtD36U3xyuo-wf7ju1dcnxxfHX2uzi9Oz44OzyvDGzJWDdFCGyqBGNQRaOuOQUexbFlNms5SpoFpQrWkFuWGBksJwUgAl7nOBd0rzmZuF_RSDdGtdFyroJ36XQjxVuk4OtODwoJzisEaxFuGZNvabGAwbrHIoakz69PMGqZ2BZ3Jv466fwZ93vFuoW7DneK0biiSGfD-ERDD9wnSqFYubdahPYQp5QkEl5wxjrP0wyw1MaQUwT7ZYKQ2l1Wby6r5sln9bnuyJ-2fO2bBt1kQwzqvOxgH41otwxR9TtXXy4vLO-aIyiyMaio5Vw9umD2YcilNoMi25V_26H_0f038CxSp0gQ</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Emfinger, Christopher H.</creator><creator>Welscher, Alecia</creator><creator>Yan, Zihan</creator><creator>Wang, Yixi</creator><creator>Conway, Hannah</creator><creator>Moss, Jennifer B.</creator><creator>Moss, Larry G.</creator><creator>Remedi, Maria S.</creator><creator>Nichols, Colin G.</creator><general>The Royal Society Publishing</general><general>The Royal Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4929-2134</orcidid></search><sort><creationdate>20170201</creationdate><title>Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells</title><author>Emfinger, Christopher H. ; Welscher, Alecia ; Yan, Zihan ; Wang, Yixi ; Conway, Hannah ; Moss, Jennifer B. ; Moss, Larry G. ; Remedi, Maria S. ; Nichols, Colin G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-72a8ac39e2c0d2eb6d4ed319b4627df34ae4a23a93f0ed3aef322108e594a2583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biochemistry And Biophysics</topic><topic>Ion Channels</topic><topic>katp</topic><topic>Metabolism</topic><topic>Pancreas</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Emfinger, Christopher H.</creatorcontrib><creatorcontrib>Welscher, Alecia</creatorcontrib><creatorcontrib>Yan, Zihan</creatorcontrib><creatorcontrib>Wang, Yixi</creatorcontrib><creatorcontrib>Conway, Hannah</creatorcontrib><creatorcontrib>Moss, Jennifer B.</creatorcontrib><creatorcontrib>Moss, Larry G.</creatorcontrib><creatorcontrib>Remedi, Maria S.</creatorcontrib><creatorcontrib>Nichols, Colin G.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Royal Society open science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Emfinger, Christopher H.</au><au>Welscher, Alecia</au><au>Yan, Zihan</au><au>Wang, Yixi</au><au>Conway, Hannah</au><au>Moss, Jennifer B.</au><au>Moss, Larry G.</au><au>Remedi, Maria S.</au><au>Nichols, Colin G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells</atitle><jtitle>Royal Society open science</jtitle><stitle>R. Soc. open sci</stitle><addtitle>R Soc Open Sci</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>4</volume><issue>2</issue><spage>160808</spage><epage>160808</epage><pages>160808-160808</pages><issn>2054-5703</issn><eissn>2054-5703</eissn><abstract>ATP-sensitive potassium channels (KATP channels) are critical nutrient sensors in many mammalian tissues. In the pancreas, KATP channels are essential for coupling glucose metabolism to insulin secretion. While orthologous genes for many components of metabolism–secretion coupling in mammals are present in lower vertebrates, their expression, functionality and ultimate impact on body glucose homeostasis are unclear. In this paper, we demonstrate that zebrafish islet β-cells express functional KATP channels of similar subunit composition, structure and metabolic sensitivity to their mammalian counterparts. We further show that pharmacological activation of native zebrafish KATP using diazoxide, a specific KATP channel opener, is sufficient to disturb glucose tolerance in adult zebrafish. That β-cell KATP channel expression and function are conserved between zebrafish and mammals illustrates the evolutionary conservation of islet metabolic sensing from fish to humans, and lends relevance to the use of zebrafish to model islet glucose sensing and diseases of membrane excitability such as neonatal diabetes.</abstract><cop>England</cop><pub>The Royal Society Publishing</pub><pmid>28386438</pmid><doi>10.1098/rsos.160808</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4929-2134</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry And Biophysics Ion Channels katp Metabolism Pancreas Zebrafish |
title | Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells |
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