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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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2012-08, Vol.61 (8), p.2093-2104
Hauptverfasser: GALLOWAY, Chad A, LEE, Hakjoo, NEJJAR, Souad, BONG SOOK JHUN, TIANZHENG YU, HSU, Wei, YOON, Yisang
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container_issue 8
container_start_page 2093
container_title Diabetes (New York, N.Y.)
container_volume 61
creator GALLOWAY, Chad A
LEE, Hakjoo
NEJJAR, Souad
BONG SOOK JHUN
TIANZHENG YU
HSU, Wei
YOON, Yisang
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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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&amp;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. 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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. 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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.</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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