Spontaneous NA+ transients in individual mitochondria of intact astrocytes
Mitochondria in intact cells maintain low Na+ levels despite the large electrochemical gradient favoring cation influx into the matrix. In addition, they display individual spontaneous transient depolarizations. The authors report here that individual mitochondria in living astrocytes exhibit sponta...
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Veröffentlicht in: | Glia 2008-02, Vol.56 (3), p.342-353 |
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description | Mitochondria in intact cells maintain low Na+ levels despite the large electrochemical gradient favoring cation influx into the matrix. In addition, they display individual spontaneous transient depolarizations. The authors report here that individual mitochondria in living astrocytes exhibit spontaneous increases in their Na+ concentration (Na mit+ spiking), as measured using the mitochondrial probe CoroNa Red. In a field of view with ∼30 astrocytes, up to 1,400 transients per minute were typically detected under resting conditions. Na mit+ spiking was also observed in neurons, but was scarce in two nonneural cell types tested. Astrocytic Na mit+ spikes averaged 12.2 ± 0.8 s in duration and 35.5 ± 3.2 mM in amplitude and coincided with brief mitochondrial depolarizations; they were impaired by mitochondrial depolarization and ruthenium red pointing to the involvement of a cation uniporter. Na mit+ spiking activity was significantly inhibited by mitochondrial Na+/H+ exchanger inhibition and sensitive to cellular pH and Na+ concentration. Ca2+ played a permissive role on Na mit+ spiking activity. Finally, the authors present evidence suggesting that Na mit+ spiking frequency was correlated with cellular ATP levels. This study shows that, under physiological conditions, individual mitochondria in living astrocytes exhibit fast Na+ exchange across their inner membrane, which reveals a new form of highly dynamic and localized functional regulation. © 2007 Wiley‐Liss, Inc. |
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In addition, they display individual spontaneous transient depolarizations. The authors report here that individual mitochondria in living astrocytes exhibit spontaneous increases in their Na+ concentration (Na mit+ spiking), as measured using the mitochondrial probe CoroNa Red. In a field of view with ∼30 astrocytes, up to 1,400 transients per minute were typically detected under resting conditions. Na mit+ spiking was also observed in neurons, but was scarce in two nonneural cell types tested. Astrocytic Na mit+ spikes averaged 12.2 ± 0.8 s in duration and 35.5 ± 3.2 mM in amplitude and coincided with brief mitochondrial depolarizations; they were impaired by mitochondrial depolarization and ruthenium red pointing to the involvement of a cation uniporter. Na mit+ spiking activity was significantly inhibited by mitochondrial Na+/H+ exchanger inhibition and sensitive to cellular pH and Na+ concentration. Ca2+ played a permissive role on Na mit+ spiking activity. Finally, the authors present evidence suggesting that Na mit+ spiking frequency was correlated with cellular ATP levels. This study shows that, under physiological conditions, individual mitochondria in living astrocytes exhibit fast Na+ exchange across their inner membrane, which reveals a new form of highly dynamic and localized functional regulation. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.20619</identifier><identifier>PMID: 18098123</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Animals, Newborn ; Astrocytes - drug effects ; Astrocytes - ultrastructure ; ATP ; calcium ; Cells, Cultured ; Cerebral Cortex - cytology ; fluorescence microscopy ; glia ; Imaging, Three-Dimensional ; Mice ; Mice, Inbred C57BL ; Mitochondria - drug effects ; Mitochondria - metabolism ; mitochondrial potential ; Models, Neurological ; neurons ; Ruthenium Red ; Signal Transduction - physiology ; sodium ; Sodium - metabolism ; Time Factors ; Uncoupling Agents - pharmacology</subject><ispartof>Glia, 2008-02, Vol.56 (3), p.342-353</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4019-4d8f79c593940ce81b218d1aa861c985640084c2fce8924e9b4e6b21d262d4cb3</citedby><cites>FETCH-LOGICAL-c4019-4d8f79c593940ce81b218d1aa861c985640084c2fce8924e9b4e6b21d262d4cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fglia.20619$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fglia.20619$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18098123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Azarias, Guillaume</creatorcontrib><creatorcontrib>Van De Ville, Dimitri</creatorcontrib><creatorcontrib>Unser, Michael</creatorcontrib><creatorcontrib>Chatton, Jean-Yves</creatorcontrib><title>Spontaneous NA+ transients in individual mitochondria of intact astrocytes</title><title>Glia</title><addtitle>Glia</addtitle><description>Mitochondria in intact cells maintain low Na+ levels despite the large electrochemical gradient favoring cation influx into the matrix. In addition, they display individual spontaneous transient depolarizations. The authors report here that individual mitochondria in living astrocytes exhibit spontaneous increases in their Na+ concentration (Na mit+ spiking), as measured using the mitochondrial probe CoroNa Red. In a field of view with ∼30 astrocytes, up to 1,400 transients per minute were typically detected under resting conditions. Na mit+ spiking was also observed in neurons, but was scarce in two nonneural cell types tested. Astrocytic Na mit+ spikes averaged 12.2 ± 0.8 s in duration and 35.5 ± 3.2 mM in amplitude and coincided with brief mitochondrial depolarizations; they were impaired by mitochondrial depolarization and ruthenium red pointing to the involvement of a cation uniporter. Na mit+ spiking activity was significantly inhibited by mitochondrial Na+/H+ exchanger inhibition and sensitive to cellular pH and Na+ concentration. Ca2+ played a permissive role on Na mit+ spiking activity. Finally, the authors present evidence suggesting that Na mit+ spiking frequency was correlated with cellular ATP levels. This study shows that, under physiological conditions, individual mitochondria in living astrocytes exhibit fast Na+ exchange across their inner membrane, which reveals a new form of highly dynamic and localized functional regulation. © 2007 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Astrocytes - drug effects</subject><subject>Astrocytes - ultrastructure</subject><subject>ATP</subject><subject>calcium</subject><subject>Cells, Cultured</subject><subject>Cerebral Cortex - cytology</subject><subject>fluorescence microscopy</subject><subject>glia</subject><subject>Imaging, Three-Dimensional</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>mitochondrial potential</subject><subject>Models, Neurological</subject><subject>neurons</subject><subject>Ruthenium Red</subject><subject>Signal Transduction - physiology</subject><subject>sodium</subject><subject>Sodium - metabolism</subject><subject>Time Factors</subject><subject>Uncoupling Agents - pharmacology</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1OwzAQhC0EgvJz4QFQThxAgd3ETexjVUFbVJUDICQulus4YEiTYjtA3x5DCtyQVlqt5puRdgg5RDhDgOT8sTLyLIEM-QbpIXAWI6bZJukB4zRGynGH7Dr3DIDhyLfJDrJAYZL2yNXNsqm9rHXTumg2OI28lbUzuvYuMnWYwryZopVVtDC-UU9NXVgjo6YMkpfKR9J526iV126fbJWycvpgvffI3eXF7XAcT69Hk-FgGisKyGNasDLnqs9TTkFphvMEWYFSsgwVZ_2MAjCqkjJoPKGaz6nOAlMkWVJQNU_3yHGXu7TNa6udFwvjlK6q7guRA_YZZCyAJx2obOOc1aVYWrOQdiUQxFdz4qs58d1cgI_Wqe18oYs_dF1VALAD3k2lV_9EidF0MvgJjTuPcV5__HqkfRFZnuZ9cT8biRk-pGOY3ghIPwGazYe7</recordid><startdate>200802</startdate><enddate>200802</enddate><creator>Azarias, Guillaume</creator><creator>Van De Ville, Dimitri</creator><creator>Unser, Michael</creator><creator>Chatton, Jean-Yves</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>200802</creationdate><title>Spontaneous NA+ transients in individual mitochondria of intact astrocytes</title><author>Azarias, Guillaume ; Van De Ville, Dimitri ; Unser, Michael ; Chatton, Jean-Yves</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4019-4d8f79c593940ce81b218d1aa861c985640084c2fce8924e9b4e6b21d262d4cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Astrocytes - drug effects</topic><topic>Astrocytes - ultrastructure</topic><topic>ATP</topic><topic>calcium</topic><topic>Cells, Cultured</topic><topic>Cerebral Cortex - cytology</topic><topic>fluorescence microscopy</topic><topic>glia</topic><topic>Imaging, Three-Dimensional</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>mitochondrial potential</topic><topic>Models, Neurological</topic><topic>neurons</topic><topic>Ruthenium Red</topic><topic>Signal Transduction - physiology</topic><topic>sodium</topic><topic>Sodium - metabolism</topic><topic>Time Factors</topic><topic>Uncoupling Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Azarias, Guillaume</creatorcontrib><creatorcontrib>Van De Ville, Dimitri</creatorcontrib><creatorcontrib>Unser, Michael</creatorcontrib><creatorcontrib>Chatton, Jean-Yves</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azarias, Guillaume</au><au>Van De Ville, Dimitri</au><au>Unser, Michael</au><au>Chatton, Jean-Yves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous NA+ transients in individual mitochondria of intact astrocytes</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2008-02</date><risdate>2008</risdate><volume>56</volume><issue>3</issue><spage>342</spage><epage>353</epage><pages>342-353</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><abstract>Mitochondria in intact cells maintain low Na+ levels despite the large electrochemical gradient favoring cation influx into the matrix. In addition, they display individual spontaneous transient depolarizations. The authors report here that individual mitochondria in living astrocytes exhibit spontaneous increases in their Na+ concentration (Na mit+ spiking), as measured using the mitochondrial probe CoroNa Red. In a field of view with ∼30 astrocytes, up to 1,400 transients per minute were typically detected under resting conditions. Na mit+ spiking was also observed in neurons, but was scarce in two nonneural cell types tested. Astrocytic Na mit+ spikes averaged 12.2 ± 0.8 s in duration and 35.5 ± 3.2 mM in amplitude and coincided with brief mitochondrial depolarizations; they were impaired by mitochondrial depolarization and ruthenium red pointing to the involvement of a cation uniporter. Na mit+ spiking activity was significantly inhibited by mitochondrial Na+/H+ exchanger inhibition and sensitive to cellular pH and Na+ concentration. Ca2+ played a permissive role on Na mit+ spiking activity. Finally, the authors present evidence suggesting that Na mit+ spiking frequency was correlated with cellular ATP levels. This study shows that, under physiological conditions, individual mitochondria in living astrocytes exhibit fast Na+ exchange across their inner membrane, which reveals a new form of highly dynamic and localized functional regulation. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18098123</pmid><doi>10.1002/glia.20619</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Newborn Astrocytes - drug effects Astrocytes - ultrastructure ATP calcium Cells, Cultured Cerebral Cortex - cytology fluorescence microscopy glia Imaging, Three-Dimensional Mice Mice, Inbred C57BL Mitochondria - drug effects Mitochondria - metabolism mitochondrial potential Models, Neurological neurons Ruthenium Red Signal Transduction - physiology sodium Sodium - metabolism Time Factors Uncoupling Agents - pharmacology |
title | Spontaneous NA+ transients in individual mitochondria of intact astrocytes |
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