Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure
Institut de Pharmacologie et de Toxicologie, Université de Lausanne, Lausanne, Switzerland Kellenberger, Stephan and Laurent Schild. Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure. Physiol. Rev. 82: 735-767, 2002. The recently discovered epi...
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creator | Kellenberger, Stephan Schild, Laurent |
description | Institut de Pharmacologie et de Toxicologie,
Université de Lausanne, Lausanne,
Switzerland
Kellenberger, Stephan and
Laurent Schild.
Epithelial Sodium Channel/Degenerin Family of Ion Channels: A
Variety of Functions for a Shared Structure. Physiol. Rev. 82: 735-767, 2002. The recently discovered
epithelial sodium channel (ENaC)/degenerin (DEG) gene family encodes
sodium channels involved in various cell functions in metazoans.
Subfamilies found in invertebrates or mammals are functionally
distinct. The degenerins in Caenorhabditis elegans
participate in mechanotransduction in neuronal cells, FaNaC in snails
is a ligand-gated channel activated by neuropeptides, and the
Drosophila subfamily is expressed in gonads and neurons. In
mammals, ENaC mediates Na + transport in epithelia and is
essential for sodium homeostasis. The ASIC genes encode
proton-gated cation channels in both the central and peripheral
nervous system that could be involved in pain transduction. This review
summarizes the physiological roles of the different channels belonging
to this family, their biophysical and pharmacological characteristics,
and the emerging knowledge of their molecular structure. Although
functionally different, the ENaC/DEG family members share functional
domains that are involved in the control of channel activity and in the
formation of the pore. The functional heterogeneity among the members
of the ENaC/DEG channel family provides a unique opportunity to address the molecular basis of basic channel functions such as activation by
ligands, mechanotransduction, ionic selectivity, or block by pharmacological ligands. |
doi_str_mv | 10.1152/physrev.00007.2002 |
format | Article |
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Université de Lausanne, Lausanne,
Switzerland
Kellenberger, Stephan and
Laurent Schild.
Epithelial Sodium Channel/Degenerin Family of Ion Channels: A
Variety of Functions for a Shared Structure. Physiol. Rev. 82: 735-767, 2002. The recently discovered
epithelial sodium channel (ENaC)/degenerin (DEG) gene family encodes
sodium channels involved in various cell functions in metazoans.
Subfamilies found in invertebrates or mammals are functionally
distinct. The degenerins in Caenorhabditis elegans
participate in mechanotransduction in neuronal cells, FaNaC in snails
is a ligand-gated channel activated by neuropeptides, and the
Drosophila subfamily is expressed in gonads and neurons. In
mammals, ENaC mediates Na + transport in epithelia and is
essential for sodium homeostasis. The ASIC genes encode
proton-gated cation channels in both the central and peripheral
nervous system that could be involved in pain transduction. This review
summarizes the physiological roles of the different channels belonging
to this family, their biophysical and pharmacological characteristics,
and the emerging knowledge of their molecular structure. Although
functionally different, the ENaC/DEG family members share functional
domains that are involved in the control of channel activity and in the
formation of the pore. The functional heterogeneity among the members
of the ENaC/DEG channel family provides a unique opportunity to address the molecular basis of basic channel functions such as activation by
ligands, mechanotransduction, ionic selectivity, or block by pharmacological ligands.</description><identifier>ISSN: 0031-9333</identifier><identifier>EISSN: 1522-1210</identifier><identifier>DOI: 10.1152/physrev.00007.2002</identifier><identifier>PMID: 12087134</identifier><identifier>CODEN: PHREA7</identifier><language>eng</language><publisher>United States: Am Physiological Soc</publisher><subject>Acid Sensing Ion Channels ; Amino Acid Sequence ; Analysis ; Animals ; Cells ; Cloning ; Degenerin Sodium Channels ; Epithelial Sodium Channels ; Genetic research ; Humans ; Ion channels ; Ion Channels - chemistry ; Ion Channels - genetics ; Ion Channels - metabolism ; Ions ; Methods ; Molecular Sequence Data ; Nerve Tissue Proteins - chemistry ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Physiological aspects ; Sodium ; Sodium channels ; Sodium Channels - chemistry ; Sodium Channels - genetics ; Sodium Channels - metabolism ; Structure-Activity Relationship</subject><ispartof>Physiological reviews, 2002-07, Vol.82 (3), p.735-767</ispartof><rights>COPYRIGHT 2002 American Physiological Society</rights><rights>Copyright American Physiological Society Jul 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-53eabda88e6fff3fa61e4da9bd2d99d0e0b05f63bd8899aa78de2495aefa9d993</citedby><cites>FETCH-LOGICAL-c551t-53eabda88e6fff3fa61e4da9bd2d99d0e0b05f63bd8899aa78de2495aefa9d993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12087134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kellenberger, Stephan</creatorcontrib><creatorcontrib>Schild, Laurent</creatorcontrib><title>Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure</title><title>Physiological reviews</title><addtitle>Physiol Rev</addtitle><description>Institut de Pharmacologie et de Toxicologie,
Université de Lausanne, Lausanne,
Switzerland
Kellenberger, Stephan and
Laurent Schild.
Epithelial Sodium Channel/Degenerin Family of Ion Channels: A
Variety of Functions for a Shared Structure. Physiol. Rev. 82: 735-767, 2002. The recently discovered
epithelial sodium channel (ENaC)/degenerin (DEG) gene family encodes
sodium channels involved in various cell functions in metazoans.
Subfamilies found in invertebrates or mammals are functionally
distinct. The degenerins in Caenorhabditis elegans
participate in mechanotransduction in neuronal cells, FaNaC in snails
is a ligand-gated channel activated by neuropeptides, and the
Drosophila subfamily is expressed in gonads and neurons. In
mammals, ENaC mediates Na + transport in epithelia and is
essential for sodium homeostasis. The ASIC genes encode
proton-gated cation channels in both the central and peripheral
nervous system that could be involved in pain transduction. This review
summarizes the physiological roles of the different channels belonging
to this family, their biophysical and pharmacological characteristics,
and the emerging knowledge of their molecular structure. Although
functionally different, the ENaC/DEG family members share functional
domains that are involved in the control of channel activity and in the
formation of the pore. The functional heterogeneity among the members
of the ENaC/DEG channel family provides a unique opportunity to address the molecular basis of basic channel functions such as activation by
ligands, mechanotransduction, ionic selectivity, or block by pharmacological ligands.</description><subject>Acid Sensing Ion Channels</subject><subject>Amino Acid Sequence</subject><subject>Analysis</subject><subject>Animals</subject><subject>Cells</subject><subject>Cloning</subject><subject>Degenerin Sodium Channels</subject><subject>Epithelial Sodium Channels</subject><subject>Genetic research</subject><subject>Humans</subject><subject>Ion channels</subject><subject>Ion Channels - chemistry</subject><subject>Ion Channels - genetics</subject><subject>Ion Channels - metabolism</subject><subject>Ions</subject><subject>Methods</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - chemistry</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Physiological aspects</subject><subject>Sodium</subject><subject>Sodium channels</subject><subject>Sodium Channels - chemistry</subject><subject>Sodium Channels - genetics</subject><subject>Sodium Channels - metabolism</subject><subject>Structure-Activity Relationship</subject><issn>0031-9333</issn><issn>1522-1210</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtv1DAUhSMEokPhD7BAFgs2kKkfceKwGw0dqFSJxRS2lhNfT1w5dnASYP497jyEhIq9sHTPd66OfLLsNcFLQji9Grr9GOHnEqdTLSnG9Em2SALNCSX4abbAmJG8ZoxdZC_G8T5hnJf8eXZBKBYVYcUis9eDnTpwVjm0DdrOPVp3yntwV59gBx6i9Wijeuv2KBh0E_xZHz-iFfquooXpIG1m3042-BGZEJFC205F0Gg7xbmd5ggvs2dGuRFend7L7Nvm-m79Jb_9-vlmvbrNW87JlHMGqtFKCCiNMcyokkChVd1oqutaY8AN5qZkjRairpWqhAZa1FyBUXUi2GX27rh3iOHHDOMkezu24JzyEOZRVkSUguIygW__Ae_DHH3KJikpC1EVrEjQhyO0Uw6k9SZMUbWHj1EueDA2jVeiZrXAnCQ8fwRPV0Nv28d4euTbGMZUppFDtL2Ke0mwfChZnkqWh5LlQ8nJ9OYUfG560H8tp1YTUB2Bzu66XzbCYYsNLuz2cjM7dwe_p_NmQSWTFeNy0CY53__feY5ydrA_QWnJTg</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Kellenberger, Stephan</creator><creator>Schild, Laurent</creator><general>Am Physiological Soc</general><general>American Physiological Society</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>7QP</scope><scope>7TK</scope><scope>7TS</scope><scope>7X8</scope></search><sort><creationdate>20020701</creationdate><title>Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure</title><author>Kellenberger, Stephan ; Schild, Laurent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c551t-53eabda88e6fff3fa61e4da9bd2d99d0e0b05f63bd8899aa78de2495aefa9d993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acid Sensing Ion Channels</topic><topic>Amino Acid Sequence</topic><topic>Analysis</topic><topic>Animals</topic><topic>Cells</topic><topic>Cloning</topic><topic>Degenerin Sodium Channels</topic><topic>Epithelial Sodium Channels</topic><topic>Genetic research</topic><topic>Humans</topic><topic>Ion channels</topic><topic>Ion Channels - chemistry</topic><topic>Ion Channels - genetics</topic><topic>Ion Channels - metabolism</topic><topic>Ions</topic><topic>Methods</topic><topic>Molecular Sequence Data</topic><topic>Nerve Tissue Proteins - chemistry</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Physiological aspects</topic><topic>Sodium</topic><topic>Sodium channels</topic><topic>Sodium Channels - chemistry</topic><topic>Sodium Channels - genetics</topic><topic>Sodium Channels - metabolism</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kellenberger, Stephan</creatorcontrib><creatorcontrib>Schild, Laurent</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>MEDLINE - Academic</collection><jtitle>Physiological reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kellenberger, Stephan</au><au>Schild, Laurent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure</atitle><jtitle>Physiological reviews</jtitle><addtitle>Physiol Rev</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>82</volume><issue>3</issue><spage>735</spage><epage>767</epage><pages>735-767</pages><issn>0031-9333</issn><eissn>1522-1210</eissn><coden>PHREA7</coden><abstract>Institut de Pharmacologie et de Toxicologie,
Université de Lausanne, Lausanne,
Switzerland
Kellenberger, Stephan and
Laurent Schild.
Epithelial Sodium Channel/Degenerin Family of Ion Channels: A
Variety of Functions for a Shared Structure. Physiol. Rev. 82: 735-767, 2002. The recently discovered
epithelial sodium channel (ENaC)/degenerin (DEG) gene family encodes
sodium channels involved in various cell functions in metazoans.
Subfamilies found in invertebrates or mammals are functionally
distinct. The degenerins in Caenorhabditis elegans
participate in mechanotransduction in neuronal cells, FaNaC in snails
is a ligand-gated channel activated by neuropeptides, and the
Drosophila subfamily is expressed in gonads and neurons. In
mammals, ENaC mediates Na + transport in epithelia and is
essential for sodium homeostasis. The ASIC genes encode
proton-gated cation channels in both the central and peripheral
nervous system that could be involved in pain transduction. This review
summarizes the physiological roles of the different channels belonging
to this family, their biophysical and pharmacological characteristics,
and the emerging knowledge of their molecular structure. Although
functionally different, the ENaC/DEG family members share functional
domains that are involved in the control of channel activity and in the
formation of the pore. The functional heterogeneity among the members
of the ENaC/DEG channel family provides a unique opportunity to address the molecular basis of basic channel functions such as activation by
ligands, mechanotransduction, ionic selectivity, or block by pharmacological ligands.</abstract><cop>United States</cop><pub>Am Physiological Soc</pub><pmid>12087134</pmid><doi>10.1152/physrev.00007.2002</doi><tpages>33</tpages></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Acid Sensing Ion Channels Amino Acid Sequence Analysis Animals Cells Cloning Degenerin Sodium Channels Epithelial Sodium Channels Genetic research Humans Ion channels Ion Channels - chemistry Ion Channels - genetics Ion Channels - metabolism Ions Methods Molecular Sequence Data Nerve Tissue Proteins - chemistry Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Physiological aspects Sodium Sodium channels Sodium Channels - chemistry Sodium Channels - genetics Sodium Channels - metabolism Structure-Activity Relationship |
title | Epithelial Sodium Channel/Degenerin Family of Ion Channels: A Variety of Functions for a Shared Structure |
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