Control of Developmental Speed in Zebrafish Embryos Using Different Incubation Temperatures
The zebrafish is a valuable model organism that is widely used in studies of vertebrate development. In the laboratory, zebrafish embryonic development is normally carried out at 28.5°C. In this study, we sought to determine whether it was possible to modify the speed of embryonic development throug...
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Veröffentlicht in: | Zebrafish 2021-10, Vol.18 (5), p.316-325 |
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creator | Urushibata, Hirotaro Sasaki, Kazuaki Takahashi, Eisuke Hanada, Toshikatsu Fujimoto, Takafumi Arai, Katsutoshi Yamaha, Etsuro |
description | The zebrafish is a valuable model organism that is widely used in studies of vertebrate development. In the laboratory, zebrafish embryonic development is normally carried out at 28.5°C. In this study, we sought to determine whether it was possible to modify the speed of embryonic development through the use of short- and long-term variations in incubation temperature. After incubation at 20°C–32°C, most early-stage embryos survived to the epiboly stage, whereas more than half of the embryos died at 32°C. The rate of development differed between embryos incubated at the lowest (18°C) and highest (34°C) temperatures: a difference of 60 min was observed at the 2-cell stage and 290 min at the 1k-cell stage. When blastulae that had developed at 28°C were transferred to a temperature lower than 18°C for one or more hours, they developed normally after being returned to the original 28°C. Analyses using green fluorescent protein-
buckyball
mRNA and
in situ
hybridization against
vasa
mRNA showed that primordial germ cells increase under low-temperature culture; this response may be of use for studies involving heterochronic germ cell transplantation. Our study shows that embryonic developmental speed can be slowed, which will be of value for performing time-consuming, complicated, and delicate microsurgical operations. |
doi_str_mv | 10.1089/zeb.2021.0022 |
format | Article |
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buckyball
mRNA and
in situ
hybridization against
vasa
mRNA showed that primordial germ cells increase under low-temperature culture; this response may be of use for studies involving heterochronic germ cell transplantation. Our study shows that embryonic developmental speed can be slowed, which will be of value for performing time-consuming, complicated, and delicate microsurgical operations.</description><identifier>ISSN: 1545-8547</identifier><identifier>EISSN: 1557-8542</identifier><identifier>DOI: 10.1089/zeb.2021.0022</identifier><identifier>PMID: 34491109</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc., publishers</publisher><subject>Animal embryos ; Animals ; Blastula ; Cell culture ; Danio rerio ; Embryo, Nonmammalian ; Embryogenesis ; Embryonic Development ; Embryonic growth stage ; Embryos ; Fluorescence ; Freshwater fishes ; Germ cells ; Green fluorescent protein ; Hybridization ; Incubation period ; Long-term changes ; Low temperature ; mRNA ; Original Articles ; Survival ; Temperature ; Transplantation ; Vertebrates ; Zebrafish</subject><ispartof>Zebrafish, 2021-10, Vol.18 (5), p.316-325</ispartof><rights>2021, Mary Ann Liebert, Inc., publishers</rights><rights>Copyright Mary Ann Liebert, Inc. Oct 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-3546-8434</orcidid></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/34491109$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Urushibata, Hirotaro</creatorcontrib><creatorcontrib>Sasaki, Kazuaki</creatorcontrib><creatorcontrib>Takahashi, Eisuke</creatorcontrib><creatorcontrib>Hanada, Toshikatsu</creatorcontrib><creatorcontrib>Fujimoto, Takafumi</creatorcontrib><creatorcontrib>Arai, Katsutoshi</creatorcontrib><creatorcontrib>Yamaha, Etsuro</creatorcontrib><title>Control of Developmental Speed in Zebrafish Embryos Using Different Incubation Temperatures</title><title>Zebrafish</title><addtitle>Zebrafish</addtitle><description>The zebrafish is a valuable model organism that is widely used in studies of vertebrate development. In the laboratory, zebrafish embryonic development is normally carried out at 28.5°C. In this study, we sought to determine whether it was possible to modify the speed of embryonic development through the use of short- and long-term variations in incubation temperature. After incubation at 20°C–32°C, most early-stage embryos survived to the epiboly stage, whereas more than half of the embryos died at <20°C or >32°C. The rate of development differed between embryos incubated at the lowest (18°C) and highest (34°C) temperatures: a difference of 60 min was observed at the 2-cell stage and 290 min at the 1k-cell stage. When blastulae that had developed at 28°C were transferred to a temperature lower than 18°C for one or more hours, they developed normally after being returned to the original 28°C. Analyses using green fluorescent protein-
buckyball
mRNA and
in situ
hybridization against
vasa
mRNA showed that primordial germ cells increase under low-temperature culture; this response may be of use for studies involving heterochronic germ cell transplantation. Our study shows that embryonic developmental speed can be slowed, which will be of value for performing time-consuming, complicated, and delicate microsurgical operations.</description><subject>Animal embryos</subject><subject>Animals</subject><subject>Blastula</subject><subject>Cell culture</subject><subject>Danio rerio</subject><subject>Embryo, Nonmammalian</subject><subject>Embryogenesis</subject><subject>Embryonic Development</subject><subject>Embryonic growth stage</subject><subject>Embryos</subject><subject>Fluorescence</subject><subject>Freshwater fishes</subject><subject>Germ cells</subject><subject>Green fluorescent protein</subject><subject>Hybridization</subject><subject>Incubation period</subject><subject>Long-term changes</subject><subject>Low temperature</subject><subject>mRNA</subject><subject>Original Articles</subject><subject>Survival</subject><subject>Temperature</subject><subject>Transplantation</subject><subject>Vertebrates</subject><subject>Zebrafish</subject><issn>1545-8547</issn><issn>1557-8542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMFLwzAUxoMobk6PXiXgufOlSdb0KHPqYODB7aKHkHQv2tGmNW2F-dfbsunpfTx-fB_8CLlmMGWg0rsftNMYYjYFiOMTMmZSJpGSIj4dspBDTkbkoml2AJynXJyTERciZQzSMXmfV74NVUErRx_wG4uqLtG3pqCvNeKW5p6-oQ3G5c0nXZQ27KuGbprcf9CH3DkMPUyXPuusafPK0zWWNQbTdgGbS3LmTNHg1fFOyOZxsZ4_R6uXp-X8fhWVTEEbIc9QODSKK5MaHksp0kwAsGQ7swlnCE6hNMKxNHMZcMicFUomNrbOgDF8Qm4PvXWovjpsWr2ruuD7SR1LxcQMZAI9dXOkOlviVtchL03Y6z8XPcAPwPA23hc5WgztP8hAD8Z1b1wPxvVgnP8CZ7xyng</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Urushibata, Hirotaro</creator><creator>Sasaki, Kazuaki</creator><creator>Takahashi, Eisuke</creator><creator>Hanada, Toshikatsu</creator><creator>Fujimoto, Takafumi</creator><creator>Arai, Katsutoshi</creator><creator>Yamaha, Etsuro</creator><general>Mary Ann Liebert, Inc., publishers</general><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QG</scope><scope>7QL</scope><scope>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-3546-8434</orcidid></search><sort><creationdate>20211001</creationdate><title>Control of Developmental Speed in Zebrafish Embryos Using Different Incubation Temperatures</title><author>Urushibata, Hirotaro ; Sasaki, Kazuaki ; Takahashi, Eisuke ; Hanada, Toshikatsu ; Fujimoto, Takafumi ; Arai, Katsutoshi ; Yamaha, Etsuro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-m180t-e3ce4fea838a9a325549c40017d6b731e0f8e5a4f19cfc030cfb4857b2bfa0aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal embryos</topic><topic>Animals</topic><topic>Blastula</topic><topic>Cell culture</topic><topic>Danio rerio</topic><topic>Embryo, Nonmammalian</topic><topic>Embryogenesis</topic><topic>Embryonic Development</topic><topic>Embryonic growth stage</topic><topic>Embryos</topic><topic>Fluorescence</topic><topic>Freshwater fishes</topic><topic>Germ cells</topic><topic>Green fluorescent protein</topic><topic>Hybridization</topic><topic>Incubation period</topic><topic>Long-term changes</topic><topic>Low temperature</topic><topic>mRNA</topic><topic>Original Articles</topic><topic>Survival</topic><topic>Temperature</topic><topic>Transplantation</topic><topic>Vertebrates</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urushibata, Hirotaro</creatorcontrib><creatorcontrib>Sasaki, Kazuaki</creatorcontrib><creatorcontrib>Takahashi, Eisuke</creatorcontrib><creatorcontrib>Hanada, Toshikatsu</creatorcontrib><creatorcontrib>Fujimoto, Takafumi</creatorcontrib><creatorcontrib>Arai, Katsutoshi</creatorcontrib><creatorcontrib>Yamaha, Etsuro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Zebrafish</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urushibata, Hirotaro</au><au>Sasaki, Kazuaki</au><au>Takahashi, Eisuke</au><au>Hanada, Toshikatsu</au><au>Fujimoto, Takafumi</au><au>Arai, Katsutoshi</au><au>Yamaha, Etsuro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Control of Developmental Speed in Zebrafish Embryos Using Different Incubation Temperatures</atitle><jtitle>Zebrafish</jtitle><addtitle>Zebrafish</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>18</volume><issue>5</issue><spage>316</spage><epage>325</epage><pages>316-325</pages><issn>1545-8547</issn><eissn>1557-8542</eissn><abstract>The zebrafish is a valuable model organism that is widely used in studies of vertebrate development. In the laboratory, zebrafish embryonic development is normally carried out at 28.5°C. In this study, we sought to determine whether it was possible to modify the speed of embryonic development through the use of short- and long-term variations in incubation temperature. After incubation at 20°C–32°C, most early-stage embryos survived to the epiboly stage, whereas more than half of the embryos died at <20°C or >32°C. The rate of development differed between embryos incubated at the lowest (18°C) and highest (34°C) temperatures: a difference of 60 min was observed at the 2-cell stage and 290 min at the 1k-cell stage. When blastulae that had developed at 28°C were transferred to a temperature lower than 18°C for one or more hours, they developed normally after being returned to the original 28°C. Analyses using green fluorescent protein-
buckyball
mRNA and
in situ
hybridization against
vasa
mRNA showed that primordial germ cells increase under low-temperature culture; this response may be of use for studies involving heterochronic germ cell transplantation. Our study shows that embryonic developmental speed can be slowed, which will be of value for performing time-consuming, complicated, and delicate microsurgical operations.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc., publishers</pub><pmid>34491109</pmid><doi>10.1089/zeb.2021.0022</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3546-8434</orcidid></addata></record> |
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subjects | Animal embryos Animals Blastula Cell culture Danio rerio Embryo, Nonmammalian Embryogenesis Embryonic Development Embryonic growth stage Embryos Fluorescence Freshwater fishes Germ cells Green fluorescent protein Hybridization Incubation period Long-term changes Low temperature mRNA Original Articles Survival Temperature Transplantation Vertebrates Zebrafish |
title | Control of Developmental Speed in Zebrafish Embryos Using Different Incubation Temperatures |
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