Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean
Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily 1 , 2 that is expressed predominantly in skeletal muscle 1 , 2 . However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustio...
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Veröffentlicht in: | Nature (London) 2000-07, Vol.406 (6794), p.415-418 |
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creator | Clapham, John C. Arch, Jonathan R. S. Chapman, Helen Haynes, Andrea Lister, Carolyn Moore, Gary B. T. Piercy, Valerie Carter, Sabrina A. Lehner, Ines Smith, Stephen A. Beeley, Lee J. Godden, Robert J. Herrity, Nicole Skehel, Mark Changani, K. Kumar Hockings, Paul D. Reid, David G. Squires, Sarah M. Hatcher, Jonathan Trail, Brenda Latcham, Judy Rastan, Sohaila Harper, Alexander J. Cadenas, Susana Buckingham, Julie A. Brand, Martin D. Abuin, Alejandro |
description | Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily
1
,
2
that is expressed predominantly in skeletal muscle
1
,
2
. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism
3
,
4
. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal. |
doi_str_mv | 10.1038/35019082 |
format | Article |
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1
,
2
that is expressed predominantly in skeletal muscle
1
,
2
. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism
3
,
4
. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/35019082</identifier><identifier>PMID: 10935638</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adipose tissue ; Adipose Tissue - metabolism ; Animals ; Animals, Genetically Modified ; Biological and medical sciences ; Blood Glucose - metabolism ; Carrier Proteins - genetics ; Carrier Proteins - physiology ; Cell metabolism, cell oxidation ; Cell physiology ; Combustion ; Energy balance ; Energy Metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Genetics ; Humanities and Social Sciences ; Humans ; Hyperphagia - genetics ; Ion Channels ; letter ; Magnetic Resonance Imaging ; Male ; Metabolism ; Mice ; Mice, Inbred C57BL ; Mitochondria - metabolism ; Mitochondrial Proteins ; Molecular and cellular biology ; multidisciplinary ; Muscle, Skeletal - physiology ; Muscular system ; Mutation ; Phenotype ; Proteins ; Rodents ; Science ; Science (multidisciplinary) ; Thinness ; UCP-3 protein ; Uncoupling Protein 3</subject><ispartof>Nature (London), 2000-07, Vol.406 (6794), p.415-418</ispartof><rights>Macmillan Magazines Ltd. 2000</rights><rights>2000 INIST-CNRS</rights><rights>COPYRIGHT 2000 Nature Publishing Group</rights><rights>Copyright Macmillan Journals Ltd. Jul 27, 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c672t-e2a51974bf3b918abd7bb42985d3496baa8907f9781469485d7d166cbea9c3f63</citedby><cites>FETCH-LOGICAL-c672t-e2a51974bf3b918abd7bb42985d3496baa8907f9781469485d7d166cbea9c3f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/35019082$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/35019082$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1504621$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10935638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clapham, John C.</creatorcontrib><creatorcontrib>Arch, Jonathan R. S.</creatorcontrib><creatorcontrib>Chapman, Helen</creatorcontrib><creatorcontrib>Haynes, Andrea</creatorcontrib><creatorcontrib>Lister, Carolyn</creatorcontrib><creatorcontrib>Moore, Gary B. T.</creatorcontrib><creatorcontrib>Piercy, Valerie</creatorcontrib><creatorcontrib>Carter, Sabrina A.</creatorcontrib><creatorcontrib>Lehner, Ines</creatorcontrib><creatorcontrib>Smith, Stephen A.</creatorcontrib><creatorcontrib>Beeley, Lee J.</creatorcontrib><creatorcontrib>Godden, Robert J.</creatorcontrib><creatorcontrib>Herrity, Nicole</creatorcontrib><creatorcontrib>Skehel, Mark</creatorcontrib><creatorcontrib>Changani, K. Kumar</creatorcontrib><creatorcontrib>Hockings, Paul D.</creatorcontrib><creatorcontrib>Reid, David G.</creatorcontrib><creatorcontrib>Squires, Sarah M.</creatorcontrib><creatorcontrib>Hatcher, Jonathan</creatorcontrib><creatorcontrib>Trail, Brenda</creatorcontrib><creatorcontrib>Latcham, Judy</creatorcontrib><creatorcontrib>Rastan, Sohaila</creatorcontrib><creatorcontrib>Harper, Alexander J.</creatorcontrib><creatorcontrib>Cadenas, Susana</creatorcontrib><creatorcontrib>Buckingham, Julie A.</creatorcontrib><creatorcontrib>Brand, Martin D.</creatorcontrib><creatorcontrib>Abuin, Alejandro</creatorcontrib><title>Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily
1
,
2
that is expressed predominantly in skeletal muscle
1
,
2
. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism
3
,
4
. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal.</description><subject>Adipose tissue</subject><subject>Adipose Tissue - metabolism</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - physiology</subject><subject>Cell metabolism, cell oxidation</subject><subject>Cell physiology</subject><subject>Combustion</subject><subject>Energy balance</subject><subject>Energy Metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Hyperphagia - genetics</subject><subject>Ion Channels</subject><subject>letter</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondrial Proteins</subject><subject>Molecular and cellular biology</subject><subject>multidisciplinary</subject><subject>Muscle, Skeletal - physiology</subject><subject>Muscular system</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Thinness</subject><subject>UCP-3 protein</subject><subject>Uncoupling Protein 3</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0luL1DAUAOAiijuugr9AgogXpGvSpLk8DoOXhVVBVwRfSpqedrKmaTdpZfffm2VGZkdXJQ-Bky8nOYeTZQ8JPiKYyle0xERhWdzKFoQJnjMuxe1sgXEhcywpP8juxXiGMS6JYHezA4IVLTmVi-zbe2sADT8gwMUYIEbrO7See-3R7M0wj-4qMIZhAutziqxH8Ts4mLRD_RyNA6QDoPXlCGFc684apH2DHGh_P7vTahfhwXY_zL68eX26epeffHx7vFqe5IaLYsqh0CVRgtUtrRWRum5EXbNCybKhTPFaa6mwaJWQhHHFUlg0hHNTg1aGtpweZs82edMvz2eIU9XbaMA57WGYYyUY5aoohUry6b8lEamR5P8wuVIlm-Dj3-DZMAefyq0KzJhkmBcJ5RvUaQeV9e0wBW068BC0Gzy0NoWXREosSSHkLumeN6M9r66joxtQWg301tyY9cXehWQmuJg6PcdYHX_-tG9f_t0uT7-uPuzr5xttwhBjgLYag-11uKwIrq7ms_o1n4k-2vZrrntorsHNQCbwZAt0NNq1QXtj486VmPGC7IqJ6cR3EHZ9_-PNn90h874</recordid><startdate>20000727</startdate><enddate>20000727</enddate><creator>Clapham, John C.</creator><creator>Arch, Jonathan R. 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Academic</collection><collection>Computer and Information Systems Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clapham, John C.</au><au>Arch, Jonathan R. S.</au><au>Chapman, Helen</au><au>Haynes, Andrea</au><au>Lister, Carolyn</au><au>Moore, Gary B. T.</au><au>Piercy, Valerie</au><au>Carter, Sabrina A.</au><au>Lehner, Ines</au><au>Smith, Stephen A.</au><au>Beeley, Lee J.</au><au>Godden, Robert J.</au><au>Herrity, Nicole</au><au>Skehel, Mark</au><au>Changani, K. Kumar</au><au>Hockings, Paul D.</au><au>Reid, David G.</au><au>Squires, Sarah M.</au><au>Hatcher, Jonathan</au><au>Trail, Brenda</au><au>Latcham, Judy</au><au>Rastan, Sohaila</au><au>Harper, Alexander J.</au><au>Cadenas, Susana</au><au>Buckingham, Julie A.</au><au>Brand, Martin D.</au><au>Abuin, Alejandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2000-07-27</date><risdate>2000</risdate><volume>406</volume><issue>6794</issue><spage>415</spage><epage>418</epage><pages>415-418</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily
1
,
2
that is expressed predominantly in skeletal muscle
1
,
2
. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism
3
,
4
. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>10935638</pmid><doi>10.1038/35019082</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 2000-07, Vol.406 (6794), p.415-418 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_proquest_miscellaneous_743692579 |
source | MEDLINE; Nature; SpringerLink Journals - AutoHoldings |
subjects | Adipose tissue Adipose Tissue - metabolism Animals Animals, Genetically Modified Biological and medical sciences Blood Glucose - metabolism Carrier Proteins - genetics Carrier Proteins - physiology Cell metabolism, cell oxidation Cell physiology Combustion Energy balance Energy Metabolism Female Fundamental and applied biological sciences. Psychology Genetics Humanities and Social Sciences Humans Hyperphagia - genetics Ion Channels letter Magnetic Resonance Imaging Male Metabolism Mice Mice, Inbred C57BL Mitochondria - metabolism Mitochondrial Proteins Molecular and cellular biology multidisciplinary Muscle, Skeletal - physiology Muscular system Mutation Phenotype Proteins Rodents Science Science (multidisciplinary) Thinness UCP-3 protein Uncoupling Protein 3 |
title | Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T20%3A07%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mice%20overexpressing%20human%20uncoupling%20protein-3%20in%20skeletal%20muscle%20are%20hyperphagic%20and%20lean&rft.jtitle=Nature%20(London)&rft.au=Clapham,%20John%20C.&rft.date=2000-07-27&rft.volume=406&rft.issue=6794&rft.spage=415&rft.epage=418&rft.pages=415-418&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/35019082&rft_dat=%3Cgale_proqu%3EA188081278%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=204484062&rft_id=info:pmid/10935638&rft_galeid=A188081278&rfr_iscdi=true |