The reverse mode of the Na+/Ca2+ exchanger provides a source of Ca2+ for store refilling following agonist-induced Ca2+ mobilization
Asthma Research Group, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, and Department of Medicine, McMaster University, Hamilton, Ontario, Canada Submitted 15 June 2006 ; accepted in final form 11 October 2006 Agonist-induced contraction of airway smooth muscle (ASM) can be...
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Veröffentlicht in: | American journal of physiology. Lung cellular and molecular physiology 2007-02, Vol.292 (2), p.L438 |
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container_title | American journal of physiology. Lung cellular and molecular physiology |
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creator | Hirota, Simon Pertens, Evi Janssen, Luke J |
description | Asthma Research Group, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, and Department of Medicine, McMaster University, Hamilton, Ontario, Canada
Submitted 15 June 2006
; accepted in final form 11 October 2006
Agonist-induced contraction of airway smooth muscle (ASM) can be triggered by an elevation in the intracellular Ca 2+ concentration, primarily through the release of Ca 2+ from the sarcoplasmic reticulum (SR). The refilling of the SR is integral for subsequent contractions. It has been suggested that Ca 2+ entry via store-operated cation (SOC) and receptor-operated cation channels may facilitate refilling of the SR. Indeed, depletion of the SR activates substantial inward SOC currents in ASM that are composed of both Ca 2+ and Na + . Accumulation of Na + within the cell may regulate Ca 2+ handling in ASM by forcing the Na + /Ca 2+ exchanger (NCX) into the reverse mode, leading to the influx of Ca 2+ from the extracellular domain. Since depletion of the SR activates substantial inward Na + current, it is conceivable that the reverse mode of the NCX may contribute to the intracellular Ca 2+ pool from which the SR is refilled. Indeed, successive contractions of bovine ASM, evoked by various agonists (ACh, histamine, 5-HT, caffeine) were significantly reduced upon removal of extracellular Na + ; whereas contractions evoked by KCl were unchanged by Na + depletion. Ouabain, a selective inhibitor of the Na + /K + pump, had no effect on the reductions observed under normal and zero-Na + conditions. KB-R7943, a selective inhibitor of the reverse mode of the NCX, significantly reduced successive contractions induced by all agonists without altering KCl responses. Furthermore, KB-R7943 abolished successive caffeine-induced Ca 2+ transients in single ASM cells. Together, these data suggest a role for the reverse mode of the NCX in refilling the SR in ASM following Ca 2+ mobilization.
calcium handling; airway smooth muscle; sodium-calcium exchanger
Address for reprint requests and other correspondence: L. J. Janssen, L-314, St. Joseph's Healthcare, 50 Charlton Ave. East, Hamilton, Ontario, Canada L8N 4A6 (e-mail: janssenl{at}mcmaster.ca ) |
doi_str_mv | 10.1152/ajplung.00222.2006 |
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Submitted 15 June 2006
; accepted in final form 11 October 2006
Agonist-induced contraction of airway smooth muscle (ASM) can be triggered by an elevation in the intracellular Ca 2+ concentration, primarily through the release of Ca 2+ from the sarcoplasmic reticulum (SR). The refilling of the SR is integral for subsequent contractions. It has been suggested that Ca 2+ entry via store-operated cation (SOC) and receptor-operated cation channels may facilitate refilling of the SR. Indeed, depletion of the SR activates substantial inward SOC currents in ASM that are composed of both Ca 2+ and Na + . Accumulation of Na + within the cell may regulate Ca 2+ handling in ASM by forcing the Na + /Ca 2+ exchanger (NCX) into the reverse mode, leading to the influx of Ca 2+ from the extracellular domain. Since depletion of the SR activates substantial inward Na + current, it is conceivable that the reverse mode of the NCX may contribute to the intracellular Ca 2+ pool from which the SR is refilled. Indeed, successive contractions of bovine ASM, evoked by various agonists (ACh, histamine, 5-HT, caffeine) were significantly reduced upon removal of extracellular Na + ; whereas contractions evoked by KCl were unchanged by Na + depletion. Ouabain, a selective inhibitor of the Na + /K + pump, had no effect on the reductions observed under normal and zero-Na + conditions. KB-R7943, a selective inhibitor of the reverse mode of the NCX, significantly reduced successive contractions induced by all agonists without altering KCl responses. Furthermore, KB-R7943 abolished successive caffeine-induced Ca 2+ transients in single ASM cells. Together, these data suggest a role for the reverse mode of the NCX in refilling the SR in ASM following Ca 2+ mobilization.
calcium handling; airway smooth muscle; sodium-calcium exchanger
Address for reprint requests and other correspondence: L. J. Janssen, L-314, St. Joseph's Healthcare, 50 Charlton Ave. East, Hamilton, Ontario, Canada L8N 4A6 (e-mail: janssenl{at}mcmaster.ca )</description><identifier>ISSN: 1040-0605</identifier><identifier>EISSN: 1522-1504</identifier><identifier>DOI: 10.1152/ajplung.00222.2006</identifier><identifier>PMID: 17041014</identifier><language>eng ; jpn</language><ispartof>American journal of physiology. Lung cellular and molecular physiology, 2007-02, Vol.292 (2), p.L438</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Hirota, Simon</creatorcontrib><creatorcontrib>Pertens, Evi</creatorcontrib><creatorcontrib>Janssen, Luke J</creatorcontrib><title>The reverse mode of the Na+/Ca2+ exchanger provides a source of Ca2+ for store refilling following agonist-induced Ca2+ mobilization</title><title>American journal of physiology. Lung cellular and molecular physiology</title><description>Asthma Research Group, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, and Department of Medicine, McMaster University, Hamilton, Ontario, Canada
Submitted 15 June 2006
; accepted in final form 11 October 2006
Agonist-induced contraction of airway smooth muscle (ASM) can be triggered by an elevation in the intracellular Ca 2+ concentration, primarily through the release of Ca 2+ from the sarcoplasmic reticulum (SR). The refilling of the SR is integral for subsequent contractions. It has been suggested that Ca 2+ entry via store-operated cation (SOC) and receptor-operated cation channels may facilitate refilling of the SR. Indeed, depletion of the SR activates substantial inward SOC currents in ASM that are composed of both Ca 2+ and Na + . Accumulation of Na + within the cell may regulate Ca 2+ handling in ASM by forcing the Na + /Ca 2+ exchanger (NCX) into the reverse mode, leading to the influx of Ca 2+ from the extracellular domain. Since depletion of the SR activates substantial inward Na + current, it is conceivable that the reverse mode of the NCX may contribute to the intracellular Ca 2+ pool from which the SR is refilled. Indeed, successive contractions of bovine ASM, evoked by various agonists (ACh, histamine, 5-HT, caffeine) were significantly reduced upon removal of extracellular Na + ; whereas contractions evoked by KCl were unchanged by Na + depletion. Ouabain, a selective inhibitor of the Na + /K + pump, had no effect on the reductions observed under normal and zero-Na + conditions. KB-R7943, a selective inhibitor of the reverse mode of the NCX, significantly reduced successive contractions induced by all agonists without altering KCl responses. Furthermore, KB-R7943 abolished successive caffeine-induced Ca 2+ transients in single ASM cells. Together, these data suggest a role for the reverse mode of the NCX in refilling the SR in ASM following Ca 2+ mobilization.
calcium handling; airway smooth muscle; sodium-calcium exchanger
Address for reprint requests and other correspondence: L. J. Janssen, L-314, St. Joseph's Healthcare, 50 Charlton Ave. East, Hamilton, Ontario, Canada L8N 4A6 (e-mail: janssenl{at}mcmaster.ca )</description><issn>1040-0605</issn><issn>1522-1504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNp1kEtPwzAQhC0EoqXwBzj5XqVdO3HrHFHFS6rgknvkOJvElRtHcfrizA8nfSBOnHY0-80chpBHBhPGBJ-qVWM3dTkB4JxPOMDsigz7Bw-YgOi61xBBADMQA3Ln_QoARA_dkgGbQ8SARUPynVRIW9xi65GuXY7UFbTrvQ81ni4UH1Pc60rVJba0ad3W5Oipot5tWn1iT0zhWuo71x6rCmOtqcves9btjkqVrja-C0ydbzTm58jaZcaaL9UZV9-Tm0JZjw-XOyLJy3OyeAuWn6_vi6dlUPEw7gIRCVFwFFLGOlRcykxIlql8pnOpmYhjMVcFhAIFsijHOYOYaUDUWSF1iOGIBOfaypTVzrSYNtXBG2ddeUgvY6Y85ilPl1Eoez7-n3_ZWJvgvvsN_uXSJi_CH6XYf1c</recordid><startdate>20070201</startdate><enddate>20070201</enddate><creator>Hirota, Simon</creator><creator>Pertens, Evi</creator><creator>Janssen, Luke J</creator><scope/></search><sort><creationdate>20070201</creationdate><title>The reverse mode of the Na+/Ca2+ exchanger provides a source of Ca2+ for store refilling following agonist-induced Ca2+ mobilization</title><author>Hirota, Simon ; Pertens, Evi ; Janssen, Luke J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h239t-5455f2e5889c3a288b581bad6cd8c159957af035e5e14de71091c0eecbf8c3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirota, Simon</creatorcontrib><creatorcontrib>Pertens, Evi</creatorcontrib><creatorcontrib>Janssen, Luke J</creatorcontrib><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirota, Simon</au><au>Pertens, Evi</au><au>Janssen, Luke J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The reverse mode of the Na+/Ca2+ exchanger provides a source of Ca2+ for store refilling following agonist-induced Ca2+ mobilization</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><date>2007-02-01</date><risdate>2007</risdate><volume>292</volume><issue>2</issue><spage>L438</spage><pages>L438-</pages><issn>1040-0605</issn><eissn>1522-1504</eissn><abstract>Asthma Research Group, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, and Department of Medicine, McMaster University, Hamilton, Ontario, Canada
Submitted 15 June 2006
; accepted in final form 11 October 2006
Agonist-induced contraction of airway smooth muscle (ASM) can be triggered by an elevation in the intracellular Ca 2+ concentration, primarily through the release of Ca 2+ from the sarcoplasmic reticulum (SR). The refilling of the SR is integral for subsequent contractions. It has been suggested that Ca 2+ entry via store-operated cation (SOC) and receptor-operated cation channels may facilitate refilling of the SR. Indeed, depletion of the SR activates substantial inward SOC currents in ASM that are composed of both Ca 2+ and Na + . Accumulation of Na + within the cell may regulate Ca 2+ handling in ASM by forcing the Na + /Ca 2+ exchanger (NCX) into the reverse mode, leading to the influx of Ca 2+ from the extracellular domain. Since depletion of the SR activates substantial inward Na + current, it is conceivable that the reverse mode of the NCX may contribute to the intracellular Ca 2+ pool from which the SR is refilled. Indeed, successive contractions of bovine ASM, evoked by various agonists (ACh, histamine, 5-HT, caffeine) were significantly reduced upon removal of extracellular Na + ; whereas contractions evoked by KCl were unchanged by Na + depletion. Ouabain, a selective inhibitor of the Na + /K + pump, had no effect on the reductions observed under normal and zero-Na + conditions. KB-R7943, a selective inhibitor of the reverse mode of the NCX, significantly reduced successive contractions induced by all agonists without altering KCl responses. Furthermore, KB-R7943 abolished successive caffeine-induced Ca 2+ transients in single ASM cells. Together, these data suggest a role for the reverse mode of the NCX in refilling the SR in ASM following Ca 2+ mobilization.
calcium handling; airway smooth muscle; sodium-calcium exchanger
Address for reprint requests and other correspondence: L. J. Janssen, L-314, St. Joseph's Healthcare, 50 Charlton Ave. East, Hamilton, Ontario, Canada L8N 4A6 (e-mail: janssenl{at}mcmaster.ca )</abstract><pmid>17041014</pmid><doi>10.1152/ajplung.00222.2006</doi></addata></record> |
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title | The reverse mode of the Na+/Ca2+ exchanger provides a source of Ca2+ for store refilling following agonist-induced Ca2+ mobilization |
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