Transgenic Control of Mitochondrial Fission Induces Mitochondrial Uncoupling and Relieves Diabetic Oxidative Stress
Mitochondria are the essential eukaryotic organelles that produce most cellular energy. The energy production and supply by mitochondria appear closely associated with the continuous shape change of mitochondria mediated by fission and fusion, as evidenced not only by the hereditary diseases caused...
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description | Mitochondria are the essential eukaryotic organelles that produce most cellular energy. The energy production and supply by mitochondria appear closely associated with the continuous shape change of mitochondria mediated by fission and fusion, as evidenced not only by the hereditary diseases caused by mutations in fission/fusion genes but also by aberrant mitochondrial morphologies associated with numerous pathologic insults. However, how morphological change of mitochondria is linked to their energy-producing activity is poorly understood. In this study, we found that perturbation of mitochondrial fission induces a unique mitochondrial uncoupling phenomenon through a large-scale fluctuation of a mitochondrial inner membrane potential. Furthermore, by genetically controlling mitochondrial fission and thereby inducing mild proton leak in mice, we were able to relieve these mice from oxidative stress in a hyperglycemic model. These findings provide mechanistic insight into how mitochondrial fission participates in regulating mitochondrial activity. In addition, these results suggest a potential application of mitochondrial fission to control mitochondrial reactive oxygen species production and oxidative stress in many human diseases. |
doi_str_mv | 10.2337/db11-1640 |
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The energy production and supply by mitochondria appear closely associated with the continuous shape change of mitochondria mediated by fission and fusion, as evidenced not only by the hereditary diseases caused by mutations in fission/fusion genes but also by aberrant mitochondrial morphologies associated with numerous pathologic insults. However, how morphological change of mitochondria is linked to their energy-producing activity is poorly understood. In this study, we found that perturbation of mitochondrial fission induces a unique mitochondrial uncoupling phenomenon through a large-scale fluctuation of a mitochondrial inner membrane potential. Furthermore, by genetically controlling mitochondrial fission and thereby inducing mild proton leak in mice, we were able to relieve these mice from oxidative stress in a hyperglycemic model. These findings provide mechanistic insight into how mitochondrial fission participates in regulating mitochondrial activity. In addition, these results suggest a potential application of mitochondrial fission to control mitochondrial reactive oxygen species production and oxidative stress in many human diseases.</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/db11-1640</identifier><identifier>PMID: 22698920</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Animals ; Biological and medical sciences ; Care and treatment ; Complications ; Complications and side effects ; Diabetes ; Diabetes. Impaired glucose tolerance ; Dynamins - genetics ; Dynamins - metabolism ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Genetic aspects ; Hypoglycemia ; Medical sciences ; Membrane Potential, Mitochondrial - physiology ; Metabolism ; Mice ; Mice, Transgenic ; Mitochondria ; Mitochondria - physiology ; Mitochondrial Membrane Transport Proteins - drug effects ; Mitochondrial Membranes - drug effects ; Mitochondrial Permeability Transition Pore ; Mitochondrial Proteins - metabolism ; Morphology ; Mutation ; Oxidative stress ; Oxidative Stress - drug effects ; Physiological aspects ; Proteins ; Protons ; Respiration ; Risk factors ; Transgenic animals ; Uncoupling Agents - pharmacology</subject><ispartof>Diabetes (New York, N.Y.), 2012-08, Vol.61 (8), p.2093-2104</ispartof><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2012 American Diabetes Association</rights><rights>COPYRIGHT 2012 American Diabetes Association</rights><rights>Copyright American Diabetes Association Aug 2012</rights><rights>2012 by the American Diabetes Association. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c676t-c35b1818ea79fadf71ea40759738400bda9757a9528fb64e0d9e4be76fc0e3443</citedby><cites>FETCH-LOGICAL-c676t-c35b1818ea79fadf71ea40759738400bda9757a9528fb64e0d9e4be76fc0e3443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402299/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402299/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26186050$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22698920$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GALLOWAY, Chad A</creatorcontrib><creatorcontrib>LEE, Hakjoo</creatorcontrib><creatorcontrib>NEJJAR, Souad</creatorcontrib><creatorcontrib>BONG SOOK JHUN</creatorcontrib><creatorcontrib>TIANZHENG YU</creatorcontrib><creatorcontrib>HSU, Wei</creatorcontrib><creatorcontrib>YOON, Yisang</creatorcontrib><title>Transgenic Control of Mitochondrial Fission Induces Mitochondrial Uncoupling and Relieves Diabetic Oxidative Stress</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Mitochondria are the essential eukaryotic organelles that produce most cellular energy. The energy production and supply by mitochondria appear closely associated with the continuous shape change of mitochondria mediated by fission and fusion, as evidenced not only by the hereditary diseases caused by mutations in fission/fusion genes but also by aberrant mitochondrial morphologies associated with numerous pathologic insults. However, how morphological change of mitochondria is linked to their energy-producing activity is poorly understood. In this study, we found that perturbation of mitochondrial fission induces a unique mitochondrial uncoupling phenomenon through a large-scale fluctuation of a mitochondrial inner membrane potential. Furthermore, by genetically controlling mitochondrial fission and thereby inducing mild proton leak in mice, we were able to relieve these mice from oxidative stress in a hyperglycemic model. These findings provide mechanistic insight into how mitochondrial fission participates in regulating mitochondrial activity. In addition, these results suggest a potential application of mitochondrial fission to control mitochondrial reactive oxygen species production and oxidative stress in many human diseases.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Care and treatment</subject><subject>Complications</subject><subject>Complications and side effects</subject><subject>Diabetes</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Dynamins - genetics</subject><subject>Dynamins - metabolism</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Genetic aspects</subject><subject>Hypoglycemia</subject><subject>Medical sciences</subject><subject>Membrane Potential, Mitochondrial - physiology</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mitochondria</subject><subject>Mitochondria - physiology</subject><subject>Mitochondrial Membrane Transport Proteins - drug effects</subject><subject>Mitochondrial Membranes - drug effects</subject><subject>Mitochondrial Permeability Transition Pore</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>Morphology</subject><subject>Mutation</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Protons</subject><subject>Respiration</subject><subject>Risk factors</subject><subject>Transgenic animals</subject><subject>Uncoupling Agents - pharmacology</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9klFrFDEQxxdR7Fl98AvIggj6sHWS7CabF6GcthZODrQF30I2O7tNySXXze5Rv705PFuvHJKHQOY3_5nJ_LPsNYETypj42DaEFISX8CSbEclkwaj4-TSbARBaECHFUfYixhsA4Ok8z44o5bKWFGZZvBy0jz16a_J58OMQXB66_Jsdg7kOvh2sdvmZjdEGn1_4djIYH0WvvAnT2lnf59q3-Xd0FjeJ-mx1g2PSXd7ZVo92g_mPccAYX2bPOu0ivtrdx9nV2ZfL-ddisTy_mJ8uCsMFHwvDqobUpEYtZKfbThDUJYhKClaXAE2rpaiElhWtu4aXCK3EskHBOwPIypIdZ5_-6K6nZoWtwTSedmo92JUefqmgrdqPeHut-rBRrARKpUwC73cCQ7idMI5qZaNB57THMEVFgIqacSogoW8foTdhGnwaL1GM0RLKqn6geu1QWd-FVNdsRdVpKgicUM4TVRyg0o4wNRk8djY97_EnB_h0WlxZczDhw15CYka8G3s9xajq88X_mtmxJjiHPaq0sPnyoLYZQowDdvf_TUBt3aq2blVbtyb2zb8Luif_2jMB73aAjka7LnnV2PjAcVJzqID9Bj4i75c</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>GALLOWAY, Chad A</creator><creator>LEE, Hakjoo</creator><creator>NEJJAR, Souad</creator><creator>BONG SOOK JHUN</creator><creator>TIANZHENG YU</creator><creator>HSU, Wei</creator><creator>YOON, Yisang</creator><general>American Diabetes Association</general><scope>IQODW</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>8GL</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120801</creationdate><title>Transgenic Control of Mitochondrial Fission Induces Mitochondrial Uncoupling and Relieves Diabetic Oxidative Stress</title><author>GALLOWAY, Chad A ; LEE, Hakjoo ; NEJJAR, Souad ; BONG SOOK JHUN ; TIANZHENG YU ; HSU, Wei ; YOON, Yisang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c676t-c35b1818ea79fadf71ea40759738400bda9757a9528fb64e0d9e4be76fc0e3443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Care and treatment</topic><topic>Complications</topic><topic>Complications and side effects</topic><topic>Diabetes</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Dynamins - genetics</topic><topic>Dynamins - metabolism</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Genetic aspects</topic><topic>Hypoglycemia</topic><topic>Medical sciences</topic><topic>Membrane Potential, Mitochondrial - physiology</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mitochondria</topic><topic>Mitochondria - physiology</topic><topic>Mitochondrial Membrane Transport Proteins - drug effects</topic><topic>Mitochondrial Membranes - drug effects</topic><topic>Mitochondrial Permeability Transition Pore</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>Morphology</topic><topic>Mutation</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Protons</topic><topic>Respiration</topic><topic>Risk factors</topic><topic>Transgenic animals</topic><topic>Uncoupling Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GALLOWAY, Chad A</creatorcontrib><creatorcontrib>LEE, Hakjoo</creatorcontrib><creatorcontrib>NEJJAR, Souad</creatorcontrib><creatorcontrib>BONG SOOK JHUN</creatorcontrib><creatorcontrib>TIANZHENG YU</creatorcontrib><creatorcontrib>HSU, Wei</creatorcontrib><creatorcontrib>YOON, Yisang</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GALLOWAY, Chad A</au><au>LEE, Hakjoo</au><au>NEJJAR, Souad</au><au>BONG SOOK JHUN</au><au>TIANZHENG YU</au><au>HSU, Wei</au><au>YOON, Yisang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transgenic Control of Mitochondrial Fission Induces Mitochondrial Uncoupling and Relieves Diabetic Oxidative Stress</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>61</volume><issue>8</issue><spage>2093</spage><epage>2104</epage><pages>2093-2104</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>Mitochondria are the essential eukaryotic organelles that produce most cellular energy. The energy production and supply by mitochondria appear closely associated with the continuous shape change of mitochondria mediated by fission and fusion, as evidenced not only by the hereditary diseases caused by mutations in fission/fusion genes but also by aberrant mitochondrial morphologies associated with numerous pathologic insults. However, how morphological change of mitochondria is linked to their energy-producing activity is poorly understood. In this study, we found that perturbation of mitochondrial fission induces a unique mitochondrial uncoupling phenomenon through a large-scale fluctuation of a mitochondrial inner membrane potential. Furthermore, by genetically controlling mitochondrial fission and thereby inducing mild proton leak in mice, we were able to relieve these mice from oxidative stress in a hyperglycemic model. These findings provide mechanistic insight into how mitochondrial fission participates in regulating mitochondrial activity. In addition, these results suggest a potential application of mitochondrial fission to control mitochondrial reactive oxygen species production and oxidative stress in many human diseases.</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>22698920</pmid><doi>10.2337/db11-1640</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Care and treatment Complications Complications and side effects Diabetes Diabetes. Impaired glucose tolerance Dynamins - genetics Dynamins - metabolism Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Genetic aspects Hypoglycemia Medical sciences Membrane Potential, Mitochondrial - physiology Metabolism Mice Mice, Transgenic Mitochondria Mitochondria - physiology Mitochondrial Membrane Transport Proteins - drug effects Mitochondrial Membranes - drug effects Mitochondrial Permeability Transition Pore Mitochondrial Proteins - metabolism Morphology Mutation Oxidative stress Oxidative Stress - drug effects Physiological aspects Proteins Protons Respiration Risk factors Transgenic animals Uncoupling Agents - pharmacology |
title | Transgenic Control of Mitochondrial Fission Induces Mitochondrial Uncoupling and Relieves Diabetic Oxidative Stress |
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