Degenerin/Epithelial Na+ Channel Proteins: Components of a Vascular Mechanosensor
Mechanosensitive ion channels are thought to mediate stretch-induced contraction in vascular smooth muscle cells (VSMCs); however, the molecular identity of the mechanosensitive ion channel complex is unknown. Although recent reports suggest degenerin/epithelial Na channel (DEG/ENaC) proteins may be...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2004-11, Vol.44 (5), p.643-648 |
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creator | Drummond, Heather A Gebremedhin, Debebe Harder, David R |
description | Mechanosensitive ion channels are thought to mediate stretch-induced contraction in vascular smooth muscle cells (VSMCs); however, the molecular identity of the mechanosensitive ion channel complex is unknown. Although recent reports suggest degenerin/epithelial Na channel (DEG/ENaC) proteins may be mechanosensors in sensory neurons, their role as mechanosensors in vascular tissue has not been examined. We first tested whether DEG/ENaC subunits are expressed in cerebral blood vessels and VSMCs and then examined their role as mechanosensors in mediating the myogenic response in intact blood vessels. Using RT-PCR, we found ENaC transcripts expressed in rat cerebral arteries and freshly dissociated rat cerebral VSMCs. We also detected ENaC expression in isolated blood vessels and VSMCs by immunoblotting and immunolocalization. Moreover, inhibition of ENaC with amiloride (1 μmol/L) and benzamil (30 nmol/L, 1 μmol), an amiloride analog, blocked myogenic constriction in isolated rat cerebral arteries. These data suggest that DEG/ENaC proteins are required for vessel responses to pressure and are consistent with the evolutionary conservation of mechanosensory function of DEG/ENaC proteins. |
doi_str_mv | 10.1161/01.HYP.0000144465.56360.ad |
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Although recent reports suggest degenerin/epithelial Na channel (DEG/ENaC) proteins may be mechanosensors in sensory neurons, their role as mechanosensors in vascular tissue has not been examined. We first tested whether DEG/ENaC subunits are expressed in cerebral blood vessels and VSMCs and then examined their role as mechanosensors in mediating the myogenic response in intact blood vessels. Using RT-PCR, we found ENaC transcripts expressed in rat cerebral arteries and freshly dissociated rat cerebral VSMCs. We also detected ENaC expression in isolated blood vessels and VSMCs by immunoblotting and immunolocalization. Moreover, inhibition of ENaC with amiloride (1 μmol/L) and benzamil (30 nmol/L, 1 μmol), an amiloride analog, blocked myogenic constriction in isolated rat cerebral arteries. These data suggest that DEG/ENaC proteins are required for vessel responses to pressure and are consistent with the evolutionary conservation of mechanosensory function of DEG/ENaC proteins.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/01.HYP.0000144465.56360.ad</identifier><identifier>PMID: 15381679</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Acid Sensing Ion Channels ; Amiloride - analogs & derivatives ; Amiloride - pharmacology ; Animals ; Cerebral Arteries - metabolism ; Degenerin Sodium Channels ; Epithelial Sodium Channels ; In Vitro Techniques ; Ion Channels - antagonists & inhibitors ; Ion Channels - metabolism ; Mechanoreceptors ; Mechanotransduction, Cellular - physiology ; Myocytes, Smooth Muscle - metabolism ; Nerve Tissue Proteins - antagonists & inhibitors ; Nerve Tissue Proteins - metabolism ; Rats ; Rats, Sprague-Dawley ; Sodium Channels - metabolism ; Vasoconstriction - drug effects</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2004-11, Vol.44 (5), p.643-648</ispartof><rights>2004 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3443-723367c4010ad41e073a73a13dcbd1f15301837fde56c417fd4bbc0a4a2d800b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15381679$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drummond, Heather A</creatorcontrib><creatorcontrib>Gebremedhin, Debebe</creatorcontrib><creatorcontrib>Harder, David R</creatorcontrib><title>Degenerin/Epithelial Na+ Channel Proteins: Components of a Vascular Mechanosensor</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>Mechanosensitive ion channels are thought to mediate stretch-induced contraction in vascular smooth muscle cells (VSMCs); however, the molecular identity of the mechanosensitive ion channel complex is unknown. Although recent reports suggest degenerin/epithelial Na channel (DEG/ENaC) proteins may be mechanosensors in sensory neurons, their role as mechanosensors in vascular tissue has not been examined. We first tested whether DEG/ENaC subunits are expressed in cerebral blood vessels and VSMCs and then examined their role as mechanosensors in mediating the myogenic response in intact blood vessels. Using RT-PCR, we found ENaC transcripts expressed in rat cerebral arteries and freshly dissociated rat cerebral VSMCs. We also detected ENaC expression in isolated blood vessels and VSMCs by immunoblotting and immunolocalization. Moreover, inhibition of ENaC with amiloride (1 μmol/L) and benzamil (30 nmol/L, 1 μmol), an amiloride analog, blocked myogenic constriction in isolated rat cerebral arteries. These data suggest that DEG/ENaC proteins are required for vessel responses to pressure and are consistent with the evolutionary conservation of mechanosensory function of DEG/ENaC proteins.</description><subject>Acid Sensing Ion Channels</subject><subject>Amiloride - analogs & derivatives</subject><subject>Amiloride - pharmacology</subject><subject>Animals</subject><subject>Cerebral Arteries - metabolism</subject><subject>Degenerin Sodium Channels</subject><subject>Epithelial Sodium Channels</subject><subject>In Vitro Techniques</subject><subject>Ion Channels - antagonists & inhibitors</subject><subject>Ion Channels - metabolism</subject><subject>Mechanoreceptors</subject><subject>Mechanotransduction, Cellular - physiology</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Nerve Tissue Proteins - antagonists & inhibitors</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sodium Channels - metabolism</subject><subject>Vasoconstriction - drug effects</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkG1LwzAQgIMoOqd_QYof_CKtuSZNN7_JnC8w30BFP4U0vbpqlsykRfz3RjcwHFwuPHcXHkIOgWYAAk4oZFev9xmNBzjnosgKwQTNVL1BBlDkPOXxYZMMKIx5OgZ42SG7Ibyv8HKb7EDBRiDK8YA8nOMbWvStPZku226OplUmuVXHyWSurEWT3HvXYWvDaTJxi6WzaLuQuCZRybMKujfKJzeoI-wC2uD8HtlqlAm4v85D8nQxfZxcpbO7y-vJ2SzVjHOWljljotScAlU1B6QlUzGA1bqqoYk_pDBiZVNjITSHeOFVpaniKq9HlFZsSI5Wc5feffYYOrlog0ZjlEXXBylKmpeM5hE8XYHauxA8NnLp24Xy3xKo_BUqKcgoVP4LlX9Cpapj88F6S18tsP5vXRuMAF8BX8506MOH6b_Qyzkq083_RvJcjNI8ZoBYpb9LGPsBx2mBgA</recordid><startdate>200411</startdate><enddate>200411</enddate><creator>Drummond, Heather A</creator><creator>Gebremedhin, Debebe</creator><creator>Harder, David R</creator><general>American Heart Association, Inc</general><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>200411</creationdate><title>Degenerin/Epithelial Na+ Channel Proteins: Components of a Vascular Mechanosensor</title><author>Drummond, Heather A ; Gebremedhin, Debebe ; Harder, David R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3443-723367c4010ad41e073a73a13dcbd1f15301837fde56c417fd4bbc0a4a2d800b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Acid Sensing Ion Channels</topic><topic>Amiloride - analogs & derivatives</topic><topic>Amiloride - pharmacology</topic><topic>Animals</topic><topic>Cerebral Arteries - metabolism</topic><topic>Degenerin Sodium Channels</topic><topic>Epithelial Sodium Channels</topic><topic>In Vitro Techniques</topic><topic>Ion Channels - antagonists & inhibitors</topic><topic>Ion Channels - metabolism</topic><topic>Mechanoreceptors</topic><topic>Mechanotransduction, Cellular - physiology</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Nerve Tissue Proteins - antagonists & inhibitors</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sodium Channels - metabolism</topic><topic>Vasoconstriction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drummond, Heather A</creatorcontrib><creatorcontrib>Gebremedhin, Debebe</creatorcontrib><creatorcontrib>Harder, David R</creatorcontrib><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>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drummond, Heather A</au><au>Gebremedhin, Debebe</au><au>Harder, David R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Degenerin/Epithelial Na+ Channel Proteins: Components of a Vascular Mechanosensor</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>2004-11</date><risdate>2004</risdate><volume>44</volume><issue>5</issue><spage>643</spage><epage>648</epage><pages>643-648</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><abstract>Mechanosensitive ion channels are thought to mediate stretch-induced contraction in vascular smooth muscle cells (VSMCs); however, the molecular identity of the mechanosensitive ion channel complex is unknown. Although recent reports suggest degenerin/epithelial Na channel (DEG/ENaC) proteins may be mechanosensors in sensory neurons, their role as mechanosensors in vascular tissue has not been examined. We first tested whether DEG/ENaC subunits are expressed in cerebral blood vessels and VSMCs and then examined their role as mechanosensors in mediating the myogenic response in intact blood vessels. Using RT-PCR, we found ENaC transcripts expressed in rat cerebral arteries and freshly dissociated rat cerebral VSMCs. We also detected ENaC expression in isolated blood vessels and VSMCs by immunoblotting and immunolocalization. Moreover, inhibition of ENaC with amiloride (1 μmol/L) and benzamil (30 nmol/L, 1 μmol), an amiloride analog, blocked myogenic constriction in isolated rat cerebral arteries. These data suggest that DEG/ENaC proteins are required for vessel responses to pressure and are consistent with the evolutionary conservation of mechanosensory function of DEG/ENaC proteins.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>15381679</pmid><doi>10.1161/01.HYP.0000144465.56360.ad</doi><tpages>6</tpages></addata></record> |
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subjects | Acid Sensing Ion Channels Amiloride - analogs & derivatives Amiloride - pharmacology Animals Cerebral Arteries - metabolism Degenerin Sodium Channels Epithelial Sodium Channels In Vitro Techniques Ion Channels - antagonists & inhibitors Ion Channels - metabolism Mechanoreceptors Mechanotransduction, Cellular - physiology Myocytes, Smooth Muscle - metabolism Nerve Tissue Proteins - antagonists & inhibitors Nerve Tissue Proteins - metabolism Rats Rats, Sprague-Dawley Sodium Channels - metabolism Vasoconstriction - drug effects |
title | Degenerin/Epithelial Na+ Channel Proteins: Components of a Vascular Mechanosensor |
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