Respiration of permeabilized cardiomyocytes from mice: no sex differences, but substrate-dependent changes in the apparent ADP-affinity
Sex differences in cardiac physiology are getting increased attention. This study assessed whether isolated, permeabilized cardiomyocytes from male and female C57BL/6 mice differ in terms of their respiration with multiple substrates and overall intracellular diffusion restriction estimated by the a...
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description | Sex differences in cardiac physiology are getting increased attention. This study assessed whether isolated, permeabilized cardiomyocytes from male and female C57BL/6 mice differ in terms of their respiration with multiple substrates and overall intracellular diffusion restriction estimated by the apparent ADP-affinity of respiration. Using respirometry, we recorded 1) the activities of respiratory complexes I, II and IV, 2) the respiration rate with substrates fuelling either complex I, II, or I + II, and 3) the apparent ADP-affinity with substrates fuelling complex I and I + II. The respiration rates were normalized to protein content and citrate synthase (CS) activity. We found no sex differences in CS activity (a marker of mitochondrial content) normalized to protein content or in any of the respiration measurements. This suggests that cardiomyocytes from male and female mice do not differ in terms of mitochondrial respiratory capacity and apparent ADP-affinity. Pyruvate modestly lowered the respiration rate, when added to succinate, glutamate and malate. This may be explained by intramitochondrial compartmentalization caused by the formation of supercomplexes and their association with specific dehydrogenases. To our knowledge, we show for the first time that the apparent ADP-affinity was substrate-dependent. This suggests that substrates may change or regulate intracellular barriers in cardiomyocytes. |
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This study assessed whether isolated, permeabilized cardiomyocytes from male and female C57BL/6 mice differ in terms of their respiration with multiple substrates and overall intracellular diffusion restriction estimated by the apparent ADP-affinity of respiration. Using respirometry, we recorded 1) the activities of respiratory complexes I, II and IV, 2) the respiration rate with substrates fuelling either complex I, II, or I + II, and 3) the apparent ADP-affinity with substrates fuelling complex I and I + II. The respiration rates were normalized to protein content and citrate synthase (CS) activity. We found no sex differences in CS activity (a marker of mitochondrial content) normalized to protein content or in any of the respiration measurements. This suggests that cardiomyocytes from male and female mice do not differ in terms of mitochondrial respiratory capacity and apparent ADP-affinity. Pyruvate modestly lowered the respiration rate, when added to succinate, glutamate and malate. This may be explained by intramitochondrial compartmentalization caused by the formation of supercomplexes and their association with specific dehydrogenases. To our knowledge, we show for the first time that the apparent ADP-affinity was substrate-dependent. This suggests that substrates may change or regulate intracellular barriers in cardiomyocytes.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-48964-x</identifier><identifier>PMID: 31467353</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 631/443/592 ; 631/80/642/333/1465 ; 64/60 ; 9/10 ; Adenosine Diphosphate - metabolism ; Affinity ; Animals ; Cardiomyocytes ; Cell Respiration ; Citrate synthase ; Female ; Gender differences ; Humanities and Social Sciences ; Intracellular ; Male ; Mice ; Mice, Inbred C57BL ; Mitochondria ; multidisciplinary ; Myocytes, Cardiac - cytology ; Myocytes, Cardiac - metabolism ; Permeability ; Pyruvic acid ; Respiration ; Science ; Science (multidisciplinary) ; Sex Characteristics ; Sex differences ; Substrates</subject><ispartof>Scientific reports, 2019-08, Vol.9 (1), p.12592-11, Article 12592</ispartof><rights>The Author(s) 2019</rights><rights>2019. 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This study assessed whether isolated, permeabilized cardiomyocytes from male and female C57BL/6 mice differ in terms of their respiration with multiple substrates and overall intracellular diffusion restriction estimated by the apparent ADP-affinity of respiration. Using respirometry, we recorded 1) the activities of respiratory complexes I, II and IV, 2) the respiration rate with substrates fuelling either complex I, II, or I + II, and 3) the apparent ADP-affinity with substrates fuelling complex I and I + II. The respiration rates were normalized to protein content and citrate synthase (CS) activity. We found no sex differences in CS activity (a marker of mitochondrial content) normalized to protein content or in any of the respiration measurements. This suggests that cardiomyocytes from male and female mice do not differ in terms of mitochondrial respiratory capacity and apparent ADP-affinity. Pyruvate modestly lowered the respiration rate, when added to succinate, glutamate and malate. This may be explained by intramitochondrial compartmentalization caused by the formation of supercomplexes and their association with specific dehydrogenases. To our knowledge, we show for the first time that the apparent ADP-affinity was substrate-dependent. This suggests that substrates may change or regulate intracellular barriers in cardiomyocytes.</description><subject>13</subject><subject>631/443/592</subject><subject>631/80/642/333/1465</subject><subject>64/60</subject><subject>9/10</subject><subject>Adenosine Diphosphate - metabolism</subject><subject>Affinity</subject><subject>Animals</subject><subject>Cardiomyocytes</subject><subject>Cell Respiration</subject><subject>Citrate synthase</subject><subject>Female</subject><subject>Gender differences</subject><subject>Humanities and Social Sciences</subject><subject>Intracellular</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondria</subject><subject>multidisciplinary</subject><subject>Myocytes, Cardiac - cytology</subject><subject>Myocytes, Cardiac - metabolism</subject><subject>Permeability</subject><subject>Pyruvic acid</subject><subject>Respiration</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sex Characteristics</subject><subject>Sex differences</subject><subject>Substrates</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kctuFDEQRS0EIlHID7BAltiwoMGvfrFAisJTigRCsLbc5XLGUbfd2N1ohh_gt_EwIQQW1MaW69StKl9CHnL2jDPZPc-K131XMd5XqusbVW3vkGPBVF0JKcTdW_cjcprzFStRi17x_j45klw1razlMfnxCfPsk1l8DDQ6OmOa0Ax-9N_RUjDJ-jjtIuwWzNSlONHJA76gIdKMW2q9c5gwAOandFgXmtchL0UOK4szBothobAx4bKU-0CXDVIzzybt389efayMcz74ZfeA3HNmzHh6fZ6QL29efz5_V118ePv-_OyiAtWqpWoHcAJQAQMhQTEJprHGtUI6yQcAxUFJw7rWQG0Ns0NjB4HQoTO1hbqVJ-TlQXdehwktlDmSGfWc_GTSTkfj9d-Z4Df6Mn7TTcvrRnZF4Mm1QIpfV8yLnnwGHEcTMK5ZC9FJzmrFWEEf_4NexTWFst6eEqpE2xdKHChIMeeE7mYYzvTean2wWher9S-r9bYUPbq9xk3Jb2MLIA9ALqny--lP7__I_gR87bm9</recordid><startdate>20190829</startdate><enddate>20190829</enddate><creator>Karro, Niina</creator><creator>Laasmaa, Martin</creator><creator>Vendelin, Marko</creator><creator>Birkedal, Rikke</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6459-0391</orcidid></search><sort><creationdate>20190829</creationdate><title>Respiration of permeabilized cardiomyocytes from mice: no sex differences, but substrate-dependent changes in the apparent ADP-affinity</title><author>Karro, Niina ; Laasmaa, Martin ; Vendelin, Marko ; Birkedal, Rikke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-7bcf2ce4c0c23c403ca6daf723f31bcc41c43a087ac5da0db6db2ec8efa5dc573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>13</topic><topic>631/443/592</topic><topic>631/80/642/333/1465</topic><topic>64/60</topic><topic>9/10</topic><topic>Adenosine Diphosphate - metabolism</topic><topic>Affinity</topic><topic>Animals</topic><topic>Cardiomyocytes</topic><topic>Cell Respiration</topic><topic>Citrate synthase</topic><topic>Female</topic><topic>Gender differences</topic><topic>Humanities and Social Sciences</topic><topic>Intracellular</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitochondria</topic><topic>multidisciplinary</topic><topic>Myocytes, Cardiac - cytology</topic><topic>Myocytes, Cardiac - metabolism</topic><topic>Permeability</topic><topic>Pyruvic acid</topic><topic>Respiration</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sex Characteristics</topic><topic>Sex differences</topic><topic>Substrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karro, Niina</creatorcontrib><creatorcontrib>Laasmaa, Martin</creatorcontrib><creatorcontrib>Vendelin, Marko</creatorcontrib><creatorcontrib>Birkedal, Rikke</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karro, Niina</au><au>Laasmaa, Martin</au><au>Vendelin, Marko</au><au>Birkedal, Rikke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Respiration of permeabilized cardiomyocytes from mice: no sex differences, but substrate-dependent changes in the apparent ADP-affinity</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-08-29</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>12592</spage><epage>11</epage><pages>12592-11</pages><artnum>12592</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Sex differences in cardiac physiology are getting increased attention. This study assessed whether isolated, permeabilized cardiomyocytes from male and female C57BL/6 mice differ in terms of their respiration with multiple substrates and overall intracellular diffusion restriction estimated by the apparent ADP-affinity of respiration. Using respirometry, we recorded 1) the activities of respiratory complexes I, II and IV, 2) the respiration rate with substrates fuelling either complex I, II, or I + II, and 3) the apparent ADP-affinity with substrates fuelling complex I and I + II. The respiration rates were normalized to protein content and citrate synthase (CS) activity. We found no sex differences in CS activity (a marker of mitochondrial content) normalized to protein content or in any of the respiration measurements. This suggests that cardiomyocytes from male and female mice do not differ in terms of mitochondrial respiratory capacity and apparent ADP-affinity. Pyruvate modestly lowered the respiration rate, when added to succinate, glutamate and malate. This may be explained by intramitochondrial compartmentalization caused by the formation of supercomplexes and their association with specific dehydrogenases. To our knowledge, we show for the first time that the apparent ADP-affinity was substrate-dependent. This suggests that substrates may change or regulate intracellular barriers in cardiomyocytes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31467353</pmid><doi>10.1038/s41598-019-48964-x</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6459-0391</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 13 631/443/592 631/80/642/333/1465 64/60 9/10 Adenosine Diphosphate - metabolism Affinity Animals Cardiomyocytes Cell Respiration Citrate synthase Female Gender differences Humanities and Social Sciences Intracellular Male Mice Mice, Inbred C57BL Mitochondria multidisciplinary Myocytes, Cardiac - cytology Myocytes, Cardiac - metabolism Permeability Pyruvic acid Respiration Science Science (multidisciplinary) Sex Characteristics Sex differences Substrates |
title | Respiration of permeabilized cardiomyocytes from mice: no sex differences, but substrate-dependent changes in the apparent ADP-affinity |
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