S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels
Modulation of smooth muscle, L-type Ca(2+) channels (class C, Ca(V)1.2b) by thionitrite S-nitrosoglutathione (GSNO) was investigated in the human embryonic kidney 293 expression system at the level of whole-cell and single-channel currents. Extracellular administration of GSNO (2 mM) rapidly reduced...
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Veröffentlicht in: | The Journal of biological chemistry 2001-05, Vol.276 (18), p.14797 |
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description | Modulation of smooth muscle, L-type Ca(2+) channels (class C, Ca(V)1.2b) by thionitrite S-nitrosoglutathione (GSNO) was investigated in the human embryonic kidney 293 expression system at the level of whole-cell and single-channel currents. Extracellular administration of GSNO (2 mM) rapidly reduced whole-cell Ba(2+) currents through channels derived either by expression of alpha1C-b or by coexpression of alpha1C-b plus beta2a and alpha2-delta. The non-thiol nitric oxide (NO) donors 2,2-diethyl-1-nitroso-oxhydrazin (2 mM) and 3-morpholinosydnonimine-hydrochloride (2 mM), which elevated cellular cGMP levels to a similar extent as GSNO, failed to affect Ba(2+) currents significantly. Intracellular administration of copper ions, which promote decomposition of the thionitrite, antagonized its inhibitory effect, and loading of cells with high concentrations of dithiothreitol (2 mM) prevented the effect of GSNO on alpha1C-b channels. Intracellular loading of cells with oxidized glutathione (2 mM) affected neither alpha1C-b channel function nor their modulation by GSNO. Analysis of single-channel behavior revealed that GSNO inhibited Ca(2+) channels mainly by reducing open probability. The development of GSNO-induced inhibition was associated with the transient occurrence of a reduced conductance state of the channel. Our results demonstrate that GSNO modulates the alpha1 subunit of smooth muscle L-type Ca(2+) channels by an intracellular mechanism that is independent of NO release and stimulation of guanylyl cyclase. We suggest S-nitrosation of intracellularly located sulfhydryl groups as an important determinant of Ca(2+) channel gating and conductance. |
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Extracellular administration of GSNO (2 mM) rapidly reduced whole-cell Ba(2+) currents through channels derived either by expression of alpha1C-b or by coexpression of alpha1C-b plus beta2a and alpha2-delta. The non-thiol nitric oxide (NO) donors 2,2-diethyl-1-nitroso-oxhydrazin (2 mM) and 3-morpholinosydnonimine-hydrochloride (2 mM), which elevated cellular cGMP levels to a similar extent as GSNO, failed to affect Ba(2+) currents significantly. Intracellular administration of copper ions, which promote decomposition of the thionitrite, antagonized its inhibitory effect, and loading of cells with high concentrations of dithiothreitol (2 mM) prevented the effect of GSNO on alpha1C-b channels. Intracellular loading of cells with oxidized glutathione (2 mM) affected neither alpha1C-b channel function nor their modulation by GSNO. Analysis of single-channel behavior revealed that GSNO inhibited Ca(2+) channels mainly by reducing open probability. The development of GSNO-induced inhibition was associated with the transient occurrence of a reduced conductance state of the channel. Our results demonstrate that GSNO modulates the alpha1 subunit of smooth muscle L-type Ca(2+) channels by an intracellular mechanism that is independent of NO release and stimulation of guanylyl cyclase. We suggest S-nitrosation of intracellularly located sulfhydryl groups as an important determinant of Ca(2+) channel gating and conductance.</description><identifier>ISSN: 0021-9258</identifier><identifier>PMID: 11278396</identifier><language>eng</language><publisher>United States</publisher><subject>Calcium Channel Blockers - pharmacology ; Calcium Channels, L-Type - chemistry ; Calcium Channels, L-Type - physiology ; Cell Line ; Cyclic GMP - metabolism ; Humans ; Ion Channel Gating ; Nitroso Compounds - chemistry</subject><ispartof>The Journal of biological chemistry, 2001-05, Vol.276 (18), p.14797</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11278396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poteser, M</creatorcontrib><creatorcontrib>Romanin, C</creatorcontrib><creatorcontrib>Schreibmayer, W</creatorcontrib><creatorcontrib>Mayer, B</creatorcontrib><creatorcontrib>Groschner, K</creatorcontrib><title>S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Modulation of smooth muscle, L-type Ca(2+) channels (class C, Ca(V)1.2b) by thionitrite S-nitrosoglutathione (GSNO) was investigated in the human embryonic kidney 293 expression system at the level of whole-cell and single-channel currents. Extracellular administration of GSNO (2 mM) rapidly reduced whole-cell Ba(2+) currents through channels derived either by expression of alpha1C-b or by coexpression of alpha1C-b plus beta2a and alpha2-delta. The non-thiol nitric oxide (NO) donors 2,2-diethyl-1-nitroso-oxhydrazin (2 mM) and 3-morpholinosydnonimine-hydrochloride (2 mM), which elevated cellular cGMP levels to a similar extent as GSNO, failed to affect Ba(2+) currents significantly. Intracellular administration of copper ions, which promote decomposition of the thionitrite, antagonized its inhibitory effect, and loading of cells with high concentrations of dithiothreitol (2 mM) prevented the effect of GSNO on alpha1C-b channels. Intracellular loading of cells with oxidized glutathione (2 mM) affected neither alpha1C-b channel function nor their modulation by GSNO. Analysis of single-channel behavior revealed that GSNO inhibited Ca(2+) channels mainly by reducing open probability. The development of GSNO-induced inhibition was associated with the transient occurrence of a reduced conductance state of the channel. Our results demonstrate that GSNO modulates the alpha1 subunit of smooth muscle L-type Ca(2+) channels by an intracellular mechanism that is independent of NO release and stimulation of guanylyl cyclase. We suggest S-nitrosation of intracellularly located sulfhydryl groups as an important determinant of Ca(2+) channel gating and conductance.</description><subject>Calcium Channel Blockers - pharmacology</subject><subject>Calcium Channels, L-Type - chemistry</subject><subject>Calcium Channels, L-Type - physiology</subject><subject>Cell Line</subject><subject>Cyclic GMP - metabolism</subject><subject>Humans</subject><subject>Ion Channel Gating</subject><subject>Nitroso Compounds - chemistry</subject><issn>0021-9258</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j09Lw0AUxPeg2Fr9CvKOiixk_yTZPUpQKwQ82Ht5ebvbRtJNyCaHfntT1LkM84MZmCu2zjIpuJW5WbHblL6zRdqKG7YSQpZG2WLNwheP7TT2Cae2j0B9XEKX4LDkeACM7sLcTBNG8tAHmI4esBuOCALS3MxL_YKpw5SggppP58FDhY_y-QnoiDH6Lt2x64Bd8vd_vmG7t9ddteX15_tH9VLzIdcFR1KuFNL4UgRFKgSNJtfWkiw1loURggRiY7xGj-SMWzBiaDJCtJmUasMefmeHuTl5tx_G9oTjef__V_0AU9RRBg</recordid><startdate>20010504</startdate><enddate>20010504</enddate><creator>Poteser, M</creator><creator>Romanin, C</creator><creator>Schreibmayer, W</creator><creator>Mayer, B</creator><creator>Groschner, K</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20010504</creationdate><title>S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels</title><author>Poteser, M ; Romanin, C ; Schreibmayer, W ; Mayer, B ; Groschner, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p546-ac3d7128e71f3c3ff4a85499c274a76811c1aab8e4aeacd8d74aaafb0caa90223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Calcium Channel Blockers - pharmacology</topic><topic>Calcium Channels, L-Type - chemistry</topic><topic>Calcium Channels, L-Type - physiology</topic><topic>Cell Line</topic><topic>Cyclic GMP - metabolism</topic><topic>Humans</topic><topic>Ion Channel Gating</topic><topic>Nitroso Compounds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poteser, M</creatorcontrib><creatorcontrib>Romanin, C</creatorcontrib><creatorcontrib>Schreibmayer, W</creatorcontrib><creatorcontrib>Mayer, B</creatorcontrib><creatorcontrib>Groschner, K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poteser, M</au><au>Romanin, C</au><au>Schreibmayer, W</au><au>Mayer, B</au><au>Groschner, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-05-04</date><risdate>2001</risdate><volume>276</volume><issue>18</issue><spage>14797</spage><pages>14797-</pages><issn>0021-9258</issn><abstract>Modulation of smooth muscle, L-type Ca(2+) channels (class C, Ca(V)1.2b) by thionitrite S-nitrosoglutathione (GSNO) was investigated in the human embryonic kidney 293 expression system at the level of whole-cell and single-channel currents. Extracellular administration of GSNO (2 mM) rapidly reduced whole-cell Ba(2+) currents through channels derived either by expression of alpha1C-b or by coexpression of alpha1C-b plus beta2a and alpha2-delta. The non-thiol nitric oxide (NO) donors 2,2-diethyl-1-nitroso-oxhydrazin (2 mM) and 3-morpholinosydnonimine-hydrochloride (2 mM), which elevated cellular cGMP levels to a similar extent as GSNO, failed to affect Ba(2+) currents significantly. Intracellular administration of copper ions, which promote decomposition of the thionitrite, antagonized its inhibitory effect, and loading of cells with high concentrations of dithiothreitol (2 mM) prevented the effect of GSNO on alpha1C-b channels. Intracellular loading of cells with oxidized glutathione (2 mM) affected neither alpha1C-b channel function nor their modulation by GSNO. Analysis of single-channel behavior revealed that GSNO inhibited Ca(2+) channels mainly by reducing open probability. The development of GSNO-induced inhibition was associated with the transient occurrence of a reduced conductance state of the channel. Our results demonstrate that GSNO modulates the alpha1 subunit of smooth muscle L-type Ca(2+) channels by an intracellular mechanism that is independent of NO release and stimulation of guanylyl cyclase. We suggest S-nitrosation of intracellularly located sulfhydryl groups as an important determinant of Ca(2+) channel gating and conductance.</abstract><cop>United States</cop><pmid>11278396</pmid></addata></record> |
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subjects | Calcium Channel Blockers - pharmacology Calcium Channels, L-Type - chemistry Calcium Channels, L-Type - physiology Cell Line Cyclic GMP - metabolism Humans Ion Channel Gating Nitroso Compounds - chemistry |
title | S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels |
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