Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A

Wnt genes encode secreted proteins which are implicated in receptor-mediated cell-cell signaling events important in embryogenesis, but the second messenger systems modulated by Wnts have not been identified. We report that ectopic expression of Xwnt-5A in zebrafish embryos enhances the frequency of...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Developmental biology 1997-02, Vol.182 (1), p.114-120
Hauptverfasser: Slusarski, D C, Yang-Snyder, J, Busa, W B, Moon, R T
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 120
container_issue 1
container_start_page 114
container_title Developmental biology
container_volume 182
creator Slusarski, D C
Yang-Snyder, J
Busa, W B
Moon, R T
description Wnt genes encode secreted proteins which are implicated in receptor-mediated cell-cell signaling events important in embryogenesis, but the second messenger systems modulated by Wnts have not been identified. We report that ectopic expression of Xwnt-5A in zebrafish embryos enhances the frequency of intracellular Ca2+ transients in the enveloping layer of the blastodisc, whereas Xwnt-8 does not. These transients are independent of extracellular Ca2+. Consistent with the observed Ca2+ transients playing a role in responses of embryos to Xwnt-5A, we report that the ligand-activated serotonin type 1C receptor, which stimulates PI cycle activity and Ca2+ signaling independent of Wnts, phenocopies embryonic responses to Xwnt-5A. These results suggest that intercellular signaling by a subset of vertebrate Wnts involves modulation of a intracellular Ca2+ signaling pathway, which may arise from phosphatidylinositol cycle activity.
doi_str_mv 10.1006/dbio.1996.8463
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_78883978</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78883978</sourcerecordid><originalsourceid>FETCH-LOGICAL-p138t-f6a96455f06f95c4dabd8ff9ba2e49dc554c940141695d384340cf56702ba2b23</originalsourceid><addsrcrecordid>eNotjztPwzAUhT2ASimsbEieWFDCdfyIvSBVVXlIRSwgxsiO7coosUucDP33BNHpDOfTeSB0Q6AkAOLBmpBKopQoJRP0DC0BSFUQAeICXeb8DQBUSrpACwU1ZZwv0eNbslOnx5AiTh673gzHFEOLQxwH3bqum90Bb3R1j3PYR92FuMfmiL_iWPD1FTr3usvu-qQr9Pm0_di8FLv359fNelccCJVj4YVWYu7zILziLbPaWOm9MrpyTNmWc9YqBoQRobilklEGreeihmpGTEVX6O4_9zCkn8nlselD_luno0tTbmo5_1K1nMHbEziZ3tnmMIReD8fmdJj-AqY9VL4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78883978</pqid></control><display><type>article</type><title>Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Slusarski, D C ; Yang-Snyder, J ; Busa, W B ; Moon, R T</creator><creatorcontrib>Slusarski, D C ; Yang-Snyder, J ; Busa, W B ; Moon, R T</creatorcontrib><description>Wnt genes encode secreted proteins which are implicated in receptor-mediated cell-cell signaling events important in embryogenesis, but the second messenger systems modulated by Wnts have not been identified. We report that ectopic expression of Xwnt-5A in zebrafish embryos enhances the frequency of intracellular Ca2+ transients in the enveloping layer of the blastodisc, whereas Xwnt-8 does not. These transients are independent of extracellular Ca2+. Consistent with the observed Ca2+ transients playing a role in responses of embryos to Xwnt-5A, we report that the ligand-activated serotonin type 1C receptor, which stimulates PI cycle activity and Ca2+ signaling independent of Wnts, phenocopies embryonic responses to Xwnt-5A. These results suggest that intercellular signaling by a subset of vertebrate Wnts involves modulation of a intracellular Ca2+ signaling pathway, which may arise from phosphatidylinositol cycle activity.</description><identifier>ISSN: 0012-1606</identifier><identifier>DOI: 10.1006/dbio.1996.8463</identifier><identifier>PMID: 9073455</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Blastocyst - physiology ; Calcium - metabolism ; Embryo, Nonmammalian - physiology ; Proto-Oncogene Proteins - biosynthesis ; Proto-Oncogene Proteins - physiology ; Receptor, Serotonin, 5-HT2C ; Receptors, Serotonin - biosynthesis ; Receptors, Serotonin - physiology ; Signal Transduction ; Vertebrates ; Wnt Proteins ; Wnt-5a Protein ; Zebrafish</subject><ispartof>Developmental biology, 1997-02, Vol.182 (1), p.114-120</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9073455$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Slusarski, D C</creatorcontrib><creatorcontrib>Yang-Snyder, J</creatorcontrib><creatorcontrib>Busa, W B</creatorcontrib><creatorcontrib>Moon, R T</creatorcontrib><title>Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A</title><title>Developmental biology</title><addtitle>Dev Biol</addtitle><description>Wnt genes encode secreted proteins which are implicated in receptor-mediated cell-cell signaling events important in embryogenesis, but the second messenger systems modulated by Wnts have not been identified. We report that ectopic expression of Xwnt-5A in zebrafish embryos enhances the frequency of intracellular Ca2+ transients in the enveloping layer of the blastodisc, whereas Xwnt-8 does not. These transients are independent of extracellular Ca2+. Consistent with the observed Ca2+ transients playing a role in responses of embryos to Xwnt-5A, we report that the ligand-activated serotonin type 1C receptor, which stimulates PI cycle activity and Ca2+ signaling independent of Wnts, phenocopies embryonic responses to Xwnt-5A. These results suggest that intercellular signaling by a subset of vertebrate Wnts involves modulation of a intracellular Ca2+ signaling pathway, which may arise from phosphatidylinositol cycle activity.</description><subject>Animals</subject><subject>Blastocyst - physiology</subject><subject>Calcium - metabolism</subject><subject>Embryo, Nonmammalian - physiology</subject><subject>Proto-Oncogene Proteins - biosynthesis</subject><subject>Proto-Oncogene Proteins - physiology</subject><subject>Receptor, Serotonin, 5-HT2C</subject><subject>Receptors, Serotonin - biosynthesis</subject><subject>Receptors, Serotonin - physiology</subject><subject>Signal Transduction</subject><subject>Vertebrates</subject><subject>Wnt Proteins</subject><subject>Wnt-5a Protein</subject><subject>Zebrafish</subject><issn>0012-1606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotjztPwzAUhT2ASimsbEieWFDCdfyIvSBVVXlIRSwgxsiO7coosUucDP33BNHpDOfTeSB0Q6AkAOLBmpBKopQoJRP0DC0BSFUQAeICXeb8DQBUSrpACwU1ZZwv0eNbslOnx5AiTh673gzHFEOLQxwH3bqum90Bb3R1j3PYR92FuMfmiL_iWPD1FTr3usvu-qQr9Pm0_di8FLv359fNelccCJVj4YVWYu7zILziLbPaWOm9MrpyTNmWc9YqBoQRobilklEGreeihmpGTEVX6O4_9zCkn8nlselD_luno0tTbmo5_1K1nMHbEziZ3tnmMIReD8fmdJj-AqY9VL4</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>Slusarski, D C</creator><creator>Yang-Snyder, J</creator><creator>Busa, W B</creator><creator>Moon, R T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19970201</creationdate><title>Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A</title><author>Slusarski, D C ; Yang-Snyder, J ; Busa, W B ; Moon, R T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p138t-f6a96455f06f95c4dabd8ff9ba2e49dc554c940141695d384340cf56702ba2b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Blastocyst - physiology</topic><topic>Calcium - metabolism</topic><topic>Embryo, Nonmammalian - physiology</topic><topic>Proto-Oncogene Proteins - biosynthesis</topic><topic>Proto-Oncogene Proteins - physiology</topic><topic>Receptor, Serotonin, 5-HT2C</topic><topic>Receptors, Serotonin - biosynthesis</topic><topic>Receptors, Serotonin - physiology</topic><topic>Signal Transduction</topic><topic>Vertebrates</topic><topic>Wnt Proteins</topic><topic>Wnt-5a Protein</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Slusarski, D C</creatorcontrib><creatorcontrib>Yang-Snyder, J</creatorcontrib><creatorcontrib>Busa, W B</creatorcontrib><creatorcontrib>Moon, R T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Slusarski, D C</au><au>Yang-Snyder, J</au><au>Busa, W B</au><au>Moon, R T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>1997-02-01</date><risdate>1997</risdate><volume>182</volume><issue>1</issue><spage>114</spage><epage>120</epage><pages>114-120</pages><issn>0012-1606</issn><abstract>Wnt genes encode secreted proteins which are implicated in receptor-mediated cell-cell signaling events important in embryogenesis, but the second messenger systems modulated by Wnts have not been identified. We report that ectopic expression of Xwnt-5A in zebrafish embryos enhances the frequency of intracellular Ca2+ transients in the enveloping layer of the blastodisc, whereas Xwnt-8 does not. These transients are independent of extracellular Ca2+. Consistent with the observed Ca2+ transients playing a role in responses of embryos to Xwnt-5A, we report that the ligand-activated serotonin type 1C receptor, which stimulates PI cycle activity and Ca2+ signaling independent of Wnts, phenocopies embryonic responses to Xwnt-5A. These results suggest that intercellular signaling by a subset of vertebrate Wnts involves modulation of a intracellular Ca2+ signaling pathway, which may arise from phosphatidylinositol cycle activity.</abstract><cop>United States</cop><pmid>9073455</pmid><doi>10.1006/dbio.1996.8463</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0012-1606
ispartof Developmental biology, 1997-02, Vol.182 (1), p.114-120
issn 0012-1606
language eng
recordid cdi_proquest_miscellaneous_78883978
source MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals
subjects Animals
Blastocyst - physiology
Calcium - metabolism
Embryo, Nonmammalian - physiology
Proto-Oncogene Proteins - biosynthesis
Proto-Oncogene Proteins - physiology
Receptor, Serotonin, 5-HT2C
Receptors, Serotonin - biosynthesis
Receptors, Serotonin - physiology
Signal Transduction
Vertebrates
Wnt Proteins
Wnt-5a Protein
Zebrafish
title Modulation of embryonic intracellular Ca2+ signaling by Wnt-5A
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T12%3A32%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modulation%20of%20embryonic%20intracellular%20Ca2+%20signaling%20by%20Wnt-5A&rft.jtitle=Developmental%20biology&rft.au=Slusarski,%20D%20C&rft.date=1997-02-01&rft.volume=182&rft.issue=1&rft.spage=114&rft.epage=120&rft.pages=114-120&rft.issn=0012-1606&rft_id=info:doi/10.1006/dbio.1996.8463&rft_dat=%3Cproquest_pubme%3E78883978%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78883978&rft_id=info:pmid/9073455&rfr_iscdi=true