Animalizing Effect of A23187 on Sea Urchin Embryos
Pulse treatment of sea urchin embryos with 3 μM A23187 for 2 hr starting at a stage in initial 10 hr period of development at 20°C, followed by a culture in normal sea water up to the pluteus corresponding stage (45 hr after fertilization), yielded many large exogastrulae with thin embryo walls. The...
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Veröffentlicht in: | Development, growth & differentiation growth & differentiation, 1991-06, Vol.33 (3), p.283-292 |
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creator | Fujiwara, Akiko Yasumasu, Ikuo |
description | Pulse treatment of sea urchin embryos with 3 μM A23187 for 2 hr starting at a stage in initial 10 hr period of development at 20°C, followed by a culture in normal sea water up to the pluteus corresponding stage (45 hr after fertilization), yielded many large exogastrulae with thin embryo walls. The pulse treatment starting at a time between 10 and 13 hr after fertilization yielded considerable number of large prisms and gastrulae having thin embryo walls. Probably, the pulse treatment exerts stimulating effects on ectodermal cell determination in whole span of pre‐hatching period to produce animalized embryos. On the other hand, pulse treatment with A23187 in pre‐hatching period exerts stage‐specific effects on gut formation. Embryos, thus treated for 2 hr starting at stages between 3 and 5 hr after fertilization, produced quite small exoguts but those treated at stages between 7 and 8 hr formed well developed and long exoguts. In embryos treated at the other stages than above, guts or exoguts were almost the same in their size to those in normal ones. These effects of A23187 on morphogenesis were canceled by procaine, tetracaine and ruthenium red. Probably, artificial Ca2+signal induced by A23187 alters the determination of cell fates, programmed in pre‐hatching period. |
doi_str_mv | 10.1111/j.1440-169X.1991.00283.x |
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The pulse treatment starting at a time between 10 and 13 hr after fertilization yielded considerable number of large prisms and gastrulae having thin embryo walls. Probably, the pulse treatment exerts stimulating effects on ectodermal cell determination in whole span of pre‐hatching period to produce animalized embryos. On the other hand, pulse treatment with A23187 in pre‐hatching period exerts stage‐specific effects on gut formation. Embryos, thus treated for 2 hr starting at stages between 3 and 5 hr after fertilization, produced quite small exoguts but those treated at stages between 7 and 8 hr formed well developed and long exoguts. In embryos treated at the other stages than above, guts or exoguts were almost the same in their size to those in normal ones. These effects of A23187 on morphogenesis were canceled by procaine, tetracaine and ruthenium red. Probably, artificial Ca2+signal induced by A23187 alters the determination of cell fates, programmed in pre‐hatching period.</description><identifier>ISSN: 0012-1592</identifier><identifier>EISSN: 1440-169X</identifier><identifier>DOI: 10.1111/j.1440-169X.1991.00283.x</identifier><identifier>PMID: 37282189</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; cell differentiation ; development ; Echinodermata ; embryos ; Fundamental and applied biological sciences. 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The pulse treatment starting at a time between 10 and 13 hr after fertilization yielded considerable number of large prisms and gastrulae having thin embryo walls. Probably, the pulse treatment exerts stimulating effects on ectodermal cell determination in whole span of pre‐hatching period to produce animalized embryos. On the other hand, pulse treatment with A23187 in pre‐hatching period exerts stage‐specific effects on gut formation. Embryos, thus treated for 2 hr starting at stages between 3 and 5 hr after fertilization, produced quite small exoguts but those treated at stages between 7 and 8 hr formed well developed and long exoguts. In embryos treated at the other stages than above, guts or exoguts were almost the same in their size to those in normal ones. These effects of A23187 on morphogenesis were canceled by procaine, tetracaine and ruthenium red. Probably, artificial Ca2+signal induced by A23187 alters the determination of cell fates, programmed in pre‐hatching period.</description><subject>Biological and medical sciences</subject><subject>cell differentiation</subject><subject>development</subject><subject>Echinodermata</subject><subject>embryos</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hemicentrotus pulcherrimus</subject><subject>Invertebrates</subject><subject>Marine</subject><subject>morphogenesis</subject><subject>organogenesis</subject><issn>0012-1592</issn><issn>1440-169X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp9kU1LAzEQhoMotlb_guSieNk1k6T5AC-lrVUoeNCCt5DNZnXLdrduWmz99e7aWm_OZQbeh4GZByEMJIambucxcE4iEPo1Bq0hJoQqFm-OUPcQHKMuIUAj6GvaQWchzAkhnAM9RR0mqaKgdBfRQZkvbJF_5eUbHmeZdytcZXhAGSiJqxI_e4tntXvPSzxeJPW2CufoJLNF8Bf73kOz-_HL8CGaPk0eh4Np5JggLPLc0kTIJGNMW_AqkRYkF94764igUmquUge8nyYp55Jq5Sik4An3PlHash662e1d1tXH2oeVWeTB-aKwpa_WwTQnMK4FU7xBr_9FQRDKNMgGvNyD62ThU7Osm-vrrfl9SANc7QEbnC2y2pYuDwcOtOREKNFwdzvuMy_89i8nphVk5qb1YFoPphVkfgSZjRlNRs3AvgHbmX_f</recordid><startdate>199106</startdate><enddate>199106</enddate><creator>Fujiwara, Akiko</creator><creator>Yasumasu, Ikuo</creator><general>Blackwell Publishing Ltd</general><general>Japanese Society of Developmental Biologists</general><scope>IQODW</scope><scope>NPM</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>199106</creationdate><title>Animalizing Effect of A23187 on Sea Urchin Embryos</title><author>Fujiwara, Akiko ; Yasumasu, Ikuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3603-e4a2b67bf339a1e8b7a1746eecac06277948dc145dbd447298c21d1e04eeb89a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Biological and medical sciences</topic><topic>cell differentiation</topic><topic>development</topic><topic>Echinodermata</topic><topic>embryos</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hemicentrotus pulcherrimus</topic><topic>Invertebrates</topic><topic>Marine</topic><topic>morphogenesis</topic><topic>organogenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujiwara, Akiko</creatorcontrib><creatorcontrib>Yasumasu, Ikuo</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Development, growth & differentiation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujiwara, Akiko</au><au>Yasumasu, Ikuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Animalizing Effect of A23187 on Sea Urchin Embryos</atitle><jtitle>Development, growth & differentiation</jtitle><addtitle>Dev Growth Differ</addtitle><date>1991-06</date><risdate>1991</risdate><volume>33</volume><issue>3</issue><spage>283</spage><epage>292</epage><pages>283-292</pages><issn>0012-1592</issn><eissn>1440-169X</eissn><abstract>Pulse treatment of sea urchin embryos with 3 μM A23187 for 2 hr starting at a stage in initial 10 hr period of development at 20°C, followed by a culture in normal sea water up to the pluteus corresponding stage (45 hr after fertilization), yielded many large exogastrulae with thin embryo walls. The pulse treatment starting at a time between 10 and 13 hr after fertilization yielded considerable number of large prisms and gastrulae having thin embryo walls. Probably, the pulse treatment exerts stimulating effects on ectodermal cell determination in whole span of pre‐hatching period to produce animalized embryos. On the other hand, pulse treatment with A23187 in pre‐hatching period exerts stage‐specific effects on gut formation. Embryos, thus treated for 2 hr starting at stages between 3 and 5 hr after fertilization, produced quite small exoguts but those treated at stages between 7 and 8 hr formed well developed and long exoguts. In embryos treated at the other stages than above, guts or exoguts were almost the same in their size to those in normal ones. These effects of A23187 on morphogenesis were canceled by procaine, tetracaine and ruthenium red. Probably, artificial Ca2+signal induced by A23187 alters the determination of cell fates, programmed in pre‐hatching period.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>37282189</pmid><doi>10.1111/j.1440-169X.1991.00283.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Open Access Titles of Japan; Alma/SFX Local Collection |
subjects | Biological and medical sciences cell differentiation development Echinodermata embryos Fundamental and applied biological sciences. Psychology Hemicentrotus pulcherrimus Invertebrates Marine morphogenesis organogenesis |
title | Animalizing Effect of A23187 on Sea Urchin Embryos |
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