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Guanylin peptides: cyclic GMP signaling mechanisms
Guanylate cyclases (GC) serve in two different signaling pathways involving cytosolic and membrane enzymes. Membrane GCs are receptors for guanylin and atriopeptin peptides, two families of cGMP-regulating peptides. Three subclasses of guanylin peptides contain one intramolecular disulfide (lymphogu...
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Published in: | Brazilian journal of medical and biological research 1999-11, Vol.32 (11), p.1329-1336 |
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container_title | Brazilian journal of medical and biological research |
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creator | Forte, L R Freeman, R H Krause, W J London, R M |
description | Guanylate cyclases (GC) serve in two different signaling pathways involving cytosolic and membrane enzymes. Membrane GCs are receptors for guanylin and atriopeptin peptides, two families of cGMP-regulating peptides. Three subclasses of guanylin peptides contain one intramolecular disulfide (lymphoguanylin), two disulfides (guanylin and uroguanylin) and three disulfides (E. coli stable toxin, ST). The peptides activate membrane receptor-GCs and regulate intestinal Cl- and HCO3- secretion via cGMP in target enterocytes. Uroguanylin and ST also elicit diuretic and natriuretic responses in the kidney. GC-C is an intestinal receptor-GC for guanylin and uroguanylin, but GC-C may not be involved in renal cGMP pathways. A novel receptor-GC expressed in the opossum kidney (OK-GC) has been identified by molecular cloning. OK-GC cDNAs encode receptor-GCs in renal tubules that are activated by guanylins. Lymphoguanylin is highly expressed in the kidney and heart where it may influence cGMP pathways. Guanylin and uroguanylin are highly expressed in intestinal mucosa to regulate intestinal salt and water transport via paracrine actions on GC-C. Uroguanylin and guanylin are also secreted from intestinal mucosa into plasma where uroguanylin serves as an intestinal natriuretic hormone to influence body Na+ homeostasis by endocrine mechanisms. Thus, guanylin peptides control salt and water transport in the kidney and intestine mediated by cGMP via membrane receptors with intrinsic guanylate cyclase activity. |
doi_str_mv | 10.1590/S0100-879X1999001100002 |
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Membrane GCs are receptors for guanylin and atriopeptin peptides, two families of cGMP-regulating peptides. Three subclasses of guanylin peptides contain one intramolecular disulfide (lymphoguanylin), two disulfides (guanylin and uroguanylin) and three disulfides (E. coli stable toxin, ST). The peptides activate membrane receptor-GCs and regulate intestinal Cl- and HCO3- secretion via cGMP in target enterocytes. Uroguanylin and ST also elicit diuretic and natriuretic responses in the kidney. GC-C is an intestinal receptor-GC for guanylin and uroguanylin, but GC-C may not be involved in renal cGMP pathways. A novel receptor-GC expressed in the opossum kidney (OK-GC) has been identified by molecular cloning. OK-GC cDNAs encode receptor-GCs in renal tubules that are activated by guanylins. Lymphoguanylin is highly expressed in the kidney and heart where it may influence cGMP pathways. Guanylin and uroguanylin are highly expressed in intestinal mucosa to regulate intestinal salt and water transport via paracrine actions on GC-C. Uroguanylin and guanylin are also secreted from intestinal mucosa into plasma where uroguanylin serves as an intestinal natriuretic hormone to influence body Na+ homeostasis by endocrine mechanisms. Thus, guanylin peptides control salt and water transport in the kidney and intestine mediated by cGMP via membrane receptors with intrinsic guanylate cyclase activity.</description><identifier>ISSN: 0100-879X</identifier><identifier>ISSN: 1414-431X</identifier><identifier>EISSN: 0100-879X</identifier><identifier>EISSN: 1414-431X</identifier><identifier>DOI: 10.1590/S0100-879X1999001100002</identifier><identifier>PMID: 10559833</identifier><language>eng</language><publisher>Brazil: Associação Brasileira de Divulgação Científica</publisher><subject>Animals ; BIOLOGY ; chloride secretion ; Cyclic GMP - physiology ; Gastrointestinal Hormones ; guanylate cyclase ; Guanylate Cyclase - metabolism ; Guanylate Cyclase - physiology ; Intestinal Mucosa - metabolism ; intestine ; kidney ; Kidney - metabolism ; MEDICINE, RESEARCH & EXPERIMENTAL ; Mice ; Natriuretic Peptides ; Opossums ; Peptides - physiology ; Rats ; Receptors, Cell Surface - genetics ; Receptors, Cell Surface - metabolism ; Receptors, Enterotoxin ; Receptors, Guanylate Cyclase-Coupled ; Receptors, Peptide - metabolism ; RNA, Messenger - metabolism ; Signal Transduction ; sodium excretion</subject><ispartof>Brazilian journal of medical and biological research, 1999-11, Vol.32 (11), p.1329-1336</ispartof><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-8aca367086ea79c36306c1302ba396eb663295ad50fc6287678a90a16b3151353</citedby><cites>FETCH-LOGICAL-c463t-8aca367086ea79c36306c1302ba396eb663295ad50fc6287678a90a16b3151353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,24150,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10559833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Forte, L R</creatorcontrib><creatorcontrib>Freeman, R H</creatorcontrib><creatorcontrib>Krause, W J</creatorcontrib><creatorcontrib>London, R M</creatorcontrib><title>Guanylin peptides: cyclic GMP signaling mechanisms</title><title>Brazilian journal of medical and biological research</title><addtitle>Braz J Med Biol Res</addtitle><description>Guanylate cyclases (GC) serve in two different signaling pathways involving cytosolic and membrane enzymes. Membrane GCs are receptors for guanylin and atriopeptin peptides, two families of cGMP-regulating peptides. Three subclasses of guanylin peptides contain one intramolecular disulfide (lymphoguanylin), two disulfides (guanylin and uroguanylin) and three disulfides (E. coli stable toxin, ST). The peptides activate membrane receptor-GCs and regulate intestinal Cl- and HCO3- secretion via cGMP in target enterocytes. Uroguanylin and ST also elicit diuretic and natriuretic responses in the kidney. GC-C is an intestinal receptor-GC for guanylin and uroguanylin, but GC-C may not be involved in renal cGMP pathways. A novel receptor-GC expressed in the opossum kidney (OK-GC) has been identified by molecular cloning. OK-GC cDNAs encode receptor-GCs in renal tubules that are activated by guanylins. Lymphoguanylin is highly expressed in the kidney and heart where it may influence cGMP pathways. Guanylin and uroguanylin are highly expressed in intestinal mucosa to regulate intestinal salt and water transport via paracrine actions on GC-C. Uroguanylin and guanylin are also secreted from intestinal mucosa into plasma where uroguanylin serves as an intestinal natriuretic hormone to influence body Na+ homeostasis by endocrine mechanisms. Thus, guanylin peptides control salt and water transport in the kidney and intestine mediated by cGMP via membrane receptors with intrinsic guanylate cyclase activity.</description><subject>Animals</subject><subject>BIOLOGY</subject><subject>chloride secretion</subject><subject>Cyclic GMP - physiology</subject><subject>Gastrointestinal Hormones</subject><subject>guanylate cyclase</subject><subject>Guanylate Cyclase - metabolism</subject><subject>Guanylate Cyclase - physiology</subject><subject>Intestinal Mucosa - metabolism</subject><subject>intestine</subject><subject>kidney</subject><subject>Kidney - metabolism</subject><subject>MEDICINE, RESEARCH & EXPERIMENTAL</subject><subject>Mice</subject><subject>Natriuretic Peptides</subject><subject>Opossums</subject><subject>Peptides - physiology</subject><subject>Rats</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Enterotoxin</subject><subject>Receptors, Guanylate Cyclase-Coupled</subject><subject>Receptors, Peptide - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction</subject><subject>sodium excretion</subject><issn>0100-879X</issn><issn>1414-431X</issn><issn>0100-879X</issn><issn>1414-431X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9UctKAzEUDaJoffyCzspd681kcjNxJ0VrQVFQwV24yaQ1ZR510ln07x0dEUFwdV_nnPti7IzDhEsNF0_AAca50q9caw3A-xAg3WGjn8LuL_-AHca46gESMr7PDjhIqXMhRiyddVRvy1Ana7_ehMLHy8RtXRlcMrt_TGJY1tRXl0nl3RvVIVbxmO0tqIz-5NsesZeb6-fp7fjuYTafXt2NXYZiM87JkUAFOXpS2gkUgI4LSC0Jjd4iilRLKiQsHKa5QpWTBuJoBZdcSHHE5oNu0dDKrNtQUbs1DQXzlWjapaF2E1zpDQHaBUdtNdqMdKYz9HmmLAhR8MwWvdZk0Iou-LIxq6Zr-8Wi-Tqk-XPInnA-ENZt8975uDFViM6XJdW-6aJBnSqJKuuBagC6tomx9YufSTmYz1_90-L0u0VnK1_84g3PER-Ps4oB</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Forte, L R</creator><creator>Freeman, R H</creator><creator>Krause, W J</creator><creator>London, R M</creator><general>Associação Brasileira de Divulgação Científica</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><scope>GPN</scope><scope>DOA</scope></search><sort><creationdate>19991101</creationdate><title>Guanylin peptides: cyclic GMP signaling mechanisms</title><author>Forte, L R ; Freeman, R H ; Krause, W J ; London, R M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-8aca367086ea79c36306c1302ba396eb663295ad50fc6287678a90a16b3151353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>BIOLOGY</topic><topic>chloride secretion</topic><topic>Cyclic GMP - physiology</topic><topic>Gastrointestinal Hormones</topic><topic>guanylate cyclase</topic><topic>Guanylate Cyclase - metabolism</topic><topic>Guanylate Cyclase - physiology</topic><topic>Intestinal Mucosa - metabolism</topic><topic>intestine</topic><topic>kidney</topic><topic>Kidney - metabolism</topic><topic>MEDICINE, RESEARCH & EXPERIMENTAL</topic><topic>Mice</topic><topic>Natriuretic Peptides</topic><topic>Opossums</topic><topic>Peptides - physiology</topic><topic>Rats</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Receptors, Enterotoxin</topic><topic>Receptors, Guanylate Cyclase-Coupled</topic><topic>Receptors, Peptide - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction</topic><topic>sodium excretion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Forte, L R</creatorcontrib><creatorcontrib>Freeman, R H</creatorcontrib><creatorcontrib>Krause, W J</creatorcontrib><creatorcontrib>London, R M</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><collection>SciELO</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Brazilian journal of medical and biological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Forte, L R</au><au>Freeman, R H</au><au>Krause, W J</au><au>London, R M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Guanylin peptides: cyclic GMP signaling mechanisms</atitle><jtitle>Brazilian journal of medical and biological research</jtitle><addtitle>Braz J Med Biol Res</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>32</volume><issue>11</issue><spage>1329</spage><epage>1336</epage><pages>1329-1336</pages><issn>0100-879X</issn><issn>1414-431X</issn><eissn>0100-879X</eissn><eissn>1414-431X</eissn><abstract>Guanylate cyclases (GC) serve in two different signaling pathways involving cytosolic and membrane enzymes. Membrane GCs are receptors for guanylin and atriopeptin peptides, two families of cGMP-regulating peptides. Three subclasses of guanylin peptides contain one intramolecular disulfide (lymphoguanylin), two disulfides (guanylin and uroguanylin) and three disulfides (E. coli stable toxin, ST). The peptides activate membrane receptor-GCs and regulate intestinal Cl- and HCO3- secretion via cGMP in target enterocytes. Uroguanylin and ST also elicit diuretic and natriuretic responses in the kidney. GC-C is an intestinal receptor-GC for guanylin and uroguanylin, but GC-C may not be involved in renal cGMP pathways. A novel receptor-GC expressed in the opossum kidney (OK-GC) has been identified by molecular cloning. OK-GC cDNAs encode receptor-GCs in renal tubules that are activated by guanylins. Lymphoguanylin is highly expressed in the kidney and heart where it may influence cGMP pathways. Guanylin and uroguanylin are highly expressed in intestinal mucosa to regulate intestinal salt and water transport via paracrine actions on GC-C. Uroguanylin and guanylin are also secreted from intestinal mucosa into plasma where uroguanylin serves as an intestinal natriuretic hormone to influence body Na+ homeostasis by endocrine mechanisms. Thus, guanylin peptides control salt and water transport in the kidney and intestine mediated by cGMP via membrane receptors with intrinsic guanylate cyclase activity.</abstract><cop>Brazil</cop><pub>Associação Brasileira de Divulgação Científica</pub><pmid>10559833</pmid><doi>10.1590/S0100-879X1999001100002</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals BIOLOGY chloride secretion Cyclic GMP - physiology Gastrointestinal Hormones guanylate cyclase Guanylate Cyclase - metabolism Guanylate Cyclase - physiology Intestinal Mucosa - metabolism intestine kidney Kidney - metabolism MEDICINE, RESEARCH & EXPERIMENTAL Mice Natriuretic Peptides Opossums Peptides - physiology Rats Receptors, Cell Surface - genetics Receptors, Cell Surface - metabolism Receptors, Enterotoxin Receptors, Guanylate Cyclase-Coupled Receptors, Peptide - metabolism RNA, Messenger - metabolism Signal Transduction sodium excretion |
title | Guanylin peptides: cyclic GMP signaling mechanisms |
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