Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations
Multiple symmetric lipomatosis (MSL) is a rare disorder characterised by large subcutaneous fat masses in some parts of the trunk. Mitochondrial disfunction is common in MSL, but the identity of the adipose cells developing in multiple lipomas is not well known. We determined that brown adipose tiss...
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Veröffentlicht in: | Biochemical and biophysical research communications 2000-11, Vol.278 (3), p.800-802 |
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creator | Vilà, Maya R. Gámez, Josep Solano, Abelardo Playán, Ana Schwartz, Simó Santorelli, Filippo M. Cervera, Carles Casali, Carlo Montoya, Julio Villarroya, Francesc |
description | Multiple symmetric lipomatosis (MSL) is a rare disorder characterised by large subcutaneous fat masses in some parts of the trunk. Mitochondrial disfunction is common in MSL, but the identity of the adipose cells developing in multiple lipomas is not well known. We determined that brown adipose tissue-specific uncoupling protein-1 (UCP-1) mRNA is expressed in the lipoma of a multiple symmetric lipomatosis patient bearing the 8344 mutation in the tRNALys gene of mitochondrial DNA. UCP1 mRNA was not detected in normal subcutaneous fat from the same patient or in the lipoma of another patient bearing a different mutation in the same tRNALys gene. These findings implicate brown adipose cells as the origin of lipomas in a subset of patients bearing tRNALys mutations in mitochondrial DNA. |
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Mitochondrial disfunction is common in MSL, but the identity of the adipose cells developing in multiple lipomas is not well known. We determined that brown adipose tissue-specific uncoupling protein-1 (UCP-1) mRNA is expressed in the lipoma of a multiple symmetric lipomatosis patient bearing the 8344 mutation in the tRNALys gene of mitochondrial DNA. UCP1 mRNA was not detected in normal subcutaneous fat from the same patient or in the lipoma of another patient bearing a different mutation in the same tRNALys gene. These findings implicate brown adipose cells as the origin of lipomas in a subset of patients bearing tRNALys mutations in mitochondrial DNA.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.2000.3828</identifier><identifier>PMID: 11095987</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipose Tissue, Brown - metabolism ; Aged ; brown adipose tissue ; Carrier Proteins - genetics ; DNA, Mitochondrial - genetics ; Female ; Humans ; Ion Channels ; Lipomatosis, Multiple Symmetrical - genetics ; Membrane Proteins - genetics ; mitochondria ; Mitochondria - genetics ; mitochondrial DNA ; Mitochondrial Proteins ; multiple symmetric lipomatosis ; Point Mutation ; RNA, Messenger - genetics ; RNA, Transfer, Lys - genetics ; Transcription, Genetic ; tRNA Lys ; UCP-1 protein ; Uncoupling Protein 1</subject><ispartof>Biochemical and biophysical research communications, 2000-11, Vol.278 (3), p.800-802</ispartof><rights>2000 Academic Press</rights><rights>Copyright 2000 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-685cc2c261d9a09553f4d4f30ae55eb737b718a8f716d22c8611b1afdffb69203</citedby><cites>FETCH-LOGICAL-c340t-685cc2c261d9a09553f4d4f30ae55eb737b718a8f716d22c8611b1afdffb69203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/bbrc.2000.3828$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11095987$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vilà, Maya R.</creatorcontrib><creatorcontrib>Gámez, Josep</creatorcontrib><creatorcontrib>Solano, Abelardo</creatorcontrib><creatorcontrib>Playán, Ana</creatorcontrib><creatorcontrib>Schwartz, Simó</creatorcontrib><creatorcontrib>Santorelli, Filippo M.</creatorcontrib><creatorcontrib>Cervera, Carles</creatorcontrib><creatorcontrib>Casali, Carlo</creatorcontrib><creatorcontrib>Montoya, Julio</creatorcontrib><creatorcontrib>Villarroya, Francesc</creatorcontrib><title>Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Multiple symmetric lipomatosis (MSL) is a rare disorder characterised by large subcutaneous fat masses in some parts of the trunk. Mitochondrial disfunction is common in MSL, but the identity of the adipose cells developing in multiple lipomas is not well known. We determined that brown adipose tissue-specific uncoupling protein-1 (UCP-1) mRNA is expressed in the lipoma of a multiple symmetric lipomatosis patient bearing the 8344 mutation in the tRNALys gene of mitochondrial DNA. UCP1 mRNA was not detected in normal subcutaneous fat from the same patient or in the lipoma of another patient bearing a different mutation in the same tRNALys gene. These findings implicate brown adipose cells as the origin of lipomas in a subset of patients bearing tRNALys mutations in mitochondrial DNA.</description><subject>Adipose Tissue, Brown - metabolism</subject><subject>Aged</subject><subject>brown adipose tissue</subject><subject>Carrier Proteins - genetics</subject><subject>DNA, Mitochondrial - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Ion Channels</subject><subject>Lipomatosis, Multiple Symmetrical - genetics</subject><subject>Membrane Proteins - genetics</subject><subject>mitochondria</subject><subject>Mitochondria - genetics</subject><subject>mitochondrial DNA</subject><subject>Mitochondrial Proteins</subject><subject>multiple symmetric lipomatosis</subject><subject>Point Mutation</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Transfer, Lys - genetics</subject><subject>Transcription, Genetic</subject><subject>tRNA Lys</subject><subject>UCP-1 protein</subject><subject>Uncoupling Protein 1</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kElrHDEQRkVwiCeOrzkGnXzriUq9qY_essB4wcTgm1CrS7ZCt9SW1Cb-99FkBnLyqaB430fVI-QzsDUw1nzt-6DXnDG2LgUX78gKWMcKDqw6IKu8bgrewcMh-Rjjb8YAqqb7QA4hU3Un2hUZ7532yzxa90hvg09oXQF0urs-pZd_5oAxWu-odXRjZz-pSE3wE71VyaJLkZ6hCv-iKj35R3RW0yubvH7ybghWjfQiF10tKfPexU_kvVFjxOP9PCL33y5_nf8oNjfff56fbgpdViwVjai15po3MHQqH1qXphoqUzKFdY19W7Z9C0IJ00IzcK5FA9CDMoMxfdNxVh6Rk13vHPzzgjHJyUaN46gc-iVKaFsuSugyuN6BOvgYAxo5Bzup8CqBya1fufUrt37l1m8OfNk3L_2Ew398LzQDYgdg_u_FYpBRZ1UaBxtQJzl4-1b3X9nuikg</recordid><startdate>20001130</startdate><enddate>20001130</enddate><creator>Vilà, Maya R.</creator><creator>Gámez, Josep</creator><creator>Solano, Abelardo</creator><creator>Playán, Ana</creator><creator>Schwartz, Simó</creator><creator>Santorelli, Filippo M.</creator><creator>Cervera, Carles</creator><creator>Casali, Carlo</creator><creator>Montoya, Julio</creator><creator>Villarroya, Francesc</creator><general>Elsevier Inc</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>7TM</scope></search><sort><creationdate>20001130</creationdate><title>Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations</title><author>Vilà, Maya R. ; Gámez, Josep ; Solano, Abelardo ; Playán, Ana ; Schwartz, Simó ; Santorelli, Filippo M. ; Cervera, Carles ; Casali, Carlo ; Montoya, Julio ; Villarroya, Francesc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-685cc2c261d9a09553f4d4f30ae55eb737b718a8f716d22c8611b1afdffb69203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adipose Tissue, Brown - metabolism</topic><topic>Aged</topic><topic>brown adipose tissue</topic><topic>Carrier Proteins - genetics</topic><topic>DNA, Mitochondrial - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Ion Channels</topic><topic>Lipomatosis, Multiple Symmetrical - genetics</topic><topic>Membrane Proteins - genetics</topic><topic>mitochondria</topic><topic>Mitochondria - genetics</topic><topic>mitochondrial DNA</topic><topic>Mitochondrial Proteins</topic><topic>multiple symmetric lipomatosis</topic><topic>Point Mutation</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Transfer, Lys - genetics</topic><topic>Transcription, Genetic</topic><topic>tRNA Lys</topic><topic>UCP-1 protein</topic><topic>Uncoupling Protein 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vilà, Maya R.</creatorcontrib><creatorcontrib>Gámez, Josep</creatorcontrib><creatorcontrib>Solano, Abelardo</creatorcontrib><creatorcontrib>Playán, Ana</creatorcontrib><creatorcontrib>Schwartz, Simó</creatorcontrib><creatorcontrib>Santorelli, Filippo M.</creatorcontrib><creatorcontrib>Cervera, Carles</creatorcontrib><creatorcontrib>Casali, Carlo</creatorcontrib><creatorcontrib>Montoya, Julio</creatorcontrib><creatorcontrib>Villarroya, Francesc</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vilà, Maya R.</au><au>Gámez, Josep</au><au>Solano, Abelardo</au><au>Playán, Ana</au><au>Schwartz, Simó</au><au>Santorelli, Filippo M.</au><au>Cervera, Carles</au><au>Casali, Carlo</au><au>Montoya, Julio</au><au>Villarroya, Francesc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2000-11-30</date><risdate>2000</risdate><volume>278</volume><issue>3</issue><spage>800</spage><epage>802</epage><pages>800-802</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Multiple symmetric lipomatosis (MSL) is a rare disorder characterised by large subcutaneous fat masses in some parts of the trunk. Mitochondrial disfunction is common in MSL, but the identity of the adipose cells developing in multiple lipomas is not well known. We determined that brown adipose tissue-specific uncoupling protein-1 (UCP-1) mRNA is expressed in the lipoma of a multiple symmetric lipomatosis patient bearing the 8344 mutation in the tRNALys gene of mitochondrial DNA. UCP1 mRNA was not detected in normal subcutaneous fat from the same patient or in the lipoma of another patient bearing a different mutation in the same tRNALys gene. These findings implicate brown adipose cells as the origin of lipomas in a subset of patients bearing tRNALys mutations in mitochondrial DNA.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11095987</pmid><doi>10.1006/bbrc.2000.3828</doi><tpages>3</tpages></addata></record> |
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subjects | Adipose Tissue, Brown - metabolism Aged brown adipose tissue Carrier Proteins - genetics DNA, Mitochondrial - genetics Female Humans Ion Channels Lipomatosis, Multiple Symmetrical - genetics Membrane Proteins - genetics mitochondria Mitochondria - genetics mitochondrial DNA Mitochondrial Proteins multiple symmetric lipomatosis Point Mutation RNA, Messenger - genetics RNA, Transfer, Lys - genetics Transcription, Genetic tRNA Lys UCP-1 protein Uncoupling Protein 1 |
title | Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations |
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