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
Hauptverfasser: Fujiwara, Akiko, Yasumasu, Ikuo
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container_title Development, growth & differentiation
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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><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. 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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 &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Development, growth &amp; 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 &amp; 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. 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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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