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Development of an in vitro tissue culture system for hammer coral (Fimbriaphyllia ancora) ovaries
In vitro gonad culture systems have proven useful to investigate intrinsic mechanisms of sexual reproduction in animals. Here we describe development of an in vitro culture method for coral ovaries. Mesenterial tissues containing both ovaries and mesenterial filaments were microscopically isolated f...
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Published in: | Scientific reports 2021-12, Vol.11 (1), p.24338-24338, Article 24338 |
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description | In vitro gonad culture systems have proven useful to investigate intrinsic mechanisms of sexual reproduction in animals. Here we describe development of an in vitro culture method for coral ovaries. Mesenterial tissues containing both ovaries and mesenterial filaments were microscopically isolated from the scleractinian coral,
Fimbriaphyllia ancora
, and culture conditions were optimized. M199 diluted 10× (10% M199, pH 8.1) and supplemented with 25 mM HEPES and the antibiotics, ampicillin, penicillin and streptomycin, supported oocyte survival and maintained the structural integrity of ovaries during short-term culture (~ 6 days). Addition of a commercial antibiotic–antimycotic solution (Anti–Anti) and fetal bovine serum adversely affected ovary maintenance and caused tissue disintegration. Characterization of cultured ovaries showed that there is no difference in cell proliferation of ovarian somatic cells between culture Days 1 and 6. Moreover, the presence of oogonia and expression of a major yolk protein, vitellogenin, were confirmed in ovaries cultured for 6 days. This system will be useful for studying effects of a wide range of substances on coral oogenesis. |
doi_str_mv | 10.1038/s41598-021-03810-x |
format | article |
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Fimbriaphyllia ancora
, and culture conditions were optimized. M199 diluted 10× (10% M199, pH 8.1) and supplemented with 25 mM HEPES and the antibiotics, ampicillin, penicillin and streptomycin, supported oocyte survival and maintained the structural integrity of ovaries during short-term culture (~ 6 days). Addition of a commercial antibiotic–antimycotic solution (Anti–Anti) and fetal bovine serum adversely affected ovary maintenance and caused tissue disintegration. Characterization of cultured ovaries showed that there is no difference in cell proliferation of ovarian somatic cells between culture Days 1 and 6. Moreover, the presence of oogonia and expression of a major yolk protein, vitellogenin, were confirmed in ovaries cultured for 6 days. This system will be useful for studying effects of a wide range of substances on coral oogenesis.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-021-03810-x</identifier><identifier>PMID: 34934168</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/61 ; 631/80 ; Ampicillin ; Animals ; Anthozoa ; Antibiotics ; Cell culture ; Cell proliferation ; Female ; Filaments ; Humanities and Social Sciences ; In Vitro Techniques ; multidisciplinary ; Oocytes - cytology ; Oocytes - metabolism ; Oogenesis ; Oogonia ; Ovaries ; Ovary - cytology ; Ovary - metabolism ; Penicillin ; Science ; Science (multidisciplinary) ; Sexual reproduction ; Somatic cells ; Streptomycin ; Tissue culture ; Tissue Culture Techniques - methods ; Vitellogenin ; Vitellogenins - metabolism ; Yolk protein</subject><ispartof>Scientific reports, 2021-12, Vol.11 (1), p.24338-24338, Article 24338</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-b7983894ba19d30e58d4173bba0296b0aa5d42f12c7aeb7998ee991cdbf725cd3</citedby><cites>FETCH-LOGICAL-c540t-b7983894ba19d30e58d4173bba0296b0aa5d42f12c7aeb7998ee991cdbf725cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2612223478/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2612223478?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34934168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiu, Yi-Ling</creatorcontrib><creatorcontrib>Chang, Ching-Fong</creatorcontrib><creatorcontrib>Shikina, Shinya</creatorcontrib><title>Development of an in vitro tissue culture system for hammer coral (Fimbriaphyllia ancora) ovaries</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>In vitro gonad culture systems have proven useful to investigate intrinsic mechanisms of sexual reproduction in animals. Here we describe development of an in vitro culture method for coral ovaries. Mesenterial tissues containing both ovaries and mesenterial filaments were microscopically isolated from the scleractinian coral,
Fimbriaphyllia ancora
, and culture conditions were optimized. M199 diluted 10× (10% M199, pH 8.1) and supplemented with 25 mM HEPES and the antibiotics, ampicillin, penicillin and streptomycin, supported oocyte survival and maintained the structural integrity of ovaries during short-term culture (~ 6 days). Addition of a commercial antibiotic–antimycotic solution (Anti–Anti) and fetal bovine serum adversely affected ovary maintenance and caused tissue disintegration. Characterization of cultured ovaries showed that there is no difference in cell proliferation of ovarian somatic cells between culture Days 1 and 6. Moreover, the presence of oogonia and expression of a major yolk protein, vitellogenin, were confirmed in ovaries cultured for 6 days. This system will be useful for studying effects of a wide range of substances on coral oogenesis.</description><subject>631/61</subject><subject>631/80</subject><subject>Ampicillin</subject><subject>Animals</subject><subject>Anthozoa</subject><subject>Antibiotics</subject><subject>Cell culture</subject><subject>Cell proliferation</subject><subject>Female</subject><subject>Filaments</subject><subject>Humanities and Social Sciences</subject><subject>In Vitro Techniques</subject><subject>multidisciplinary</subject><subject>Oocytes - cytology</subject><subject>Oocytes - metabolism</subject><subject>Oogenesis</subject><subject>Oogonia</subject><subject>Ovaries</subject><subject>Ovary - cytology</subject><subject>Ovary - metabolism</subject><subject>Penicillin</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sexual reproduction</subject><subject>Somatic cells</subject><subject>Streptomycin</subject><subject>Tissue culture</subject><subject>Tissue Culture Techniques - methods</subject><subject>Vitellogenin</subject><subject>Vitellogenins - metabolism</subject><subject>Yolk protein</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEolXpH-CALHEphxR_5WMuSKhQqFSJC5ytiTPZ9SqJFztZdf893k0pLYf6Ynvmncf2-M2yt4JfCq7qj1GLAuqcS5GnreD53YvsVHJd5FJJ-fLR-iQ7j3HD0ygkaAGvsxOlQWlR1qcZfqEd9X470Dgx3zEcmRvZzk3Bs8nFOBOzcz_NgVjcx4kG1vnA1jgMFJj1AXt2ce2GJjjcrvd97zAhDvEPzO8wOIpvslcd9pHO7-ez7Nf1159X3_PbH99urj7f5rbQfMqbCmpVg25QQKs4FXWrRaWaBrmEsuGIRatlJ6StkJIYaiIAYdumq2RhW3WW3Szc1uPGbIMbMOyNR2eOAR9WBsPkbE8GBHANEivSQouOQGiCoqSOA6IqD6xPC2s7NwO1NjUnvfQJ9GlmdGuz8jtTlyALDglwcQ8I_vdMcTKDi5b6HkfyczSyFLKqFD9K3_8n3fg5jKlVR5WUSld1UslFZYOPMVD3cBnBzcEQZjGESYYwR0OYu1T07vEzHkr-fn8SqEUQU2pcUfh39jPYPzqewiE</recordid><startdate>20211221</startdate><enddate>20211221</enddate><creator>Chiu, Yi-Ling</creator><creator>Chang, Ching-Fong</creator><creator>Shikina, Shinya</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20211221</creationdate><title>Development of an in vitro tissue culture system for hammer coral (Fimbriaphyllia ancora) ovaries</title><author>Chiu, Yi-Ling ; Chang, Ching-Fong ; Shikina, Shinya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-b7983894ba19d30e58d4173bba0296b0aa5d42f12c7aeb7998ee991cdbf725cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/61</topic><topic>631/80</topic><topic>Ampicillin</topic><topic>Animals</topic><topic>Anthozoa</topic><topic>Antibiotics</topic><topic>Cell culture</topic><topic>Cell proliferation</topic><topic>Female</topic><topic>Filaments</topic><topic>Humanities and Social Sciences</topic><topic>In Vitro Techniques</topic><topic>multidisciplinary</topic><topic>Oocytes - cytology</topic><topic>Oocytes - metabolism</topic><topic>Oogenesis</topic><topic>Oogonia</topic><topic>Ovaries</topic><topic>Ovary - cytology</topic><topic>Ovary - metabolism</topic><topic>Penicillin</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sexual reproduction</topic><topic>Somatic cells</topic><topic>Streptomycin</topic><topic>Tissue culture</topic><topic>Tissue Culture Techniques - methods</topic><topic>Vitellogenin</topic><topic>Vitellogenins - metabolism</topic><topic>Yolk protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiu, Yi-Ling</creatorcontrib><creatorcontrib>Chang, Ching-Fong</creatorcontrib><creatorcontrib>Shikina, Shinya</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiu, Yi-Ling</au><au>Chang, Ching-Fong</au><au>Shikina, Shinya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of an in vitro tissue culture system for hammer coral (Fimbriaphyllia ancora) ovaries</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2021-12-21</date><risdate>2021</risdate><volume>11</volume><issue>1</issue><spage>24338</spage><epage>24338</epage><pages>24338-24338</pages><artnum>24338</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>In vitro gonad culture systems have proven useful to investigate intrinsic mechanisms of sexual reproduction in animals. Here we describe development of an in vitro culture method for coral ovaries. Mesenterial tissues containing both ovaries and mesenterial filaments were microscopically isolated from the scleractinian coral,
Fimbriaphyllia ancora
, and culture conditions were optimized. M199 diluted 10× (10% M199, pH 8.1) and supplemented with 25 mM HEPES and the antibiotics, ampicillin, penicillin and streptomycin, supported oocyte survival and maintained the structural integrity of ovaries during short-term culture (~ 6 days). Addition of a commercial antibiotic–antimycotic solution (Anti–Anti) and fetal bovine serum adversely affected ovary maintenance and caused tissue disintegration. Characterization of cultured ovaries showed that there is no difference in cell proliferation of ovarian somatic cells between culture Days 1 and 6. Moreover, the presence of oogonia and expression of a major yolk protein, vitellogenin, were confirmed in ovaries cultured for 6 days. This system will be useful for studying effects of a wide range of substances on coral oogenesis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>34934168</pmid><doi>10.1038/s41598-021-03810-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/61 631/80 Ampicillin Animals Anthozoa Antibiotics Cell culture Cell proliferation Female Filaments Humanities and Social Sciences In Vitro Techniques multidisciplinary Oocytes - cytology Oocytes - metabolism Oogenesis Oogonia Ovaries Ovary - cytology Ovary - metabolism Penicillin Science Science (multidisciplinary) Sexual reproduction Somatic cells Streptomycin Tissue culture Tissue Culture Techniques - methods Vitellogenin Vitellogenins - metabolism Yolk protein |
title | Development of an in vitro tissue culture system for hammer coral (Fimbriaphyllia ancora) ovaries |
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