Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells

Cryopreservation of fish sperm offers the practical applications in the selective breeding and biodiversity conservation. However, because of the lack of cryopreservation methods for fish eggs and embryos, maternally inherited cytoplasmic compartments cannot be successfully preserved. We previously...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical and biophysical research communications 2016-09, Vol.478 (3), p.1478-1483
Hauptverfasser: Lee, Seungki, Katayama, Naoto, Yoshizaki, Goro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1483
container_issue 3
container_start_page 1478
container_title Biochemical and biophysical research communications
container_volume 478
creator Lee, Seungki
Katayama, Naoto
Yoshizaki, Goro
description Cryopreservation of fish sperm offers the practical applications in the selective breeding and biodiversity conservation. However, because of the lack of cryopreservation methods for fish eggs and embryos, maternally inherited cytoplasmic compartments cannot be successfully preserved. We previously developed an alternative method to derive functional eggs and sperm from cryopreserved whole testis by transplanting testicular cells into female and male recipients. However, if target fish had ovaries, the previous method employing male-derived germ cells would be ineffective. Here, we aimed to generate functional gametes from cryopreserved whole ovaries by transplanting ovarian germ cells into peritoneal cavity of sterile hatchlings. Cryopreservation conditions for rainbow trout ovaries (1.0 M DMSO, 0.1 M trehalose, and 10% egg yolk) were optimized by testing several different cryoprotective agents. Ovarian germ cells from thawed ovaries were intraperitoneally transplanted into allogeneic triploid hatchlings. Transplanted germ cells migrated toward and were incorporated into recipient gonads, where they underwent gametogenesis. Transplantation efficiency of ovarian germ cells remained stable after cryopreservation period up to 1185 days. Although all triploid recipients that did not undergo transplantation were functionally sterile, 5 of 25 female recipients and 7 of 25 male recipients reached sexual maturity at 2.5 years post-transplantation. Inseminating the resultant eggs and sperm generated viable offspring displaying the donor characteristics of orange body color, green fluorescence, and chromosome numbers. This method is thus a breakthrough tool for the conservation of endangered fish species that are crucial to cryopreserve the genetic resources of female fish. •No methods are currently available for cryopreserving fish eggs and embryos.•Rainbow trout ovaries were cryopreserved for up to 1185 days.•Germ cells recovered from thawed ovaries were transplanted into sterile recipients.•Transplanted ovarian germ cells differentiated into functional eggs and sperm.•This method is an effective means to preserve the fish genetic resources.
doi_str_mv 10.1016/j.bbrc.2016.08.156
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1832245968</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X16314206</els_id><sourcerecordid>1819430014</sourcerecordid><originalsourceid>FETCH-LOGICAL-c613t-79d9369f61976e71e8007cc1c79c6d7196bf2a596330ab5ed56942d02946b5c33</originalsourceid><addsrcrecordid>eNqNkcGO1SAUhonROHdGX8CFYemmFWhLS-LGTHTGZBI3mrgjFE6Vm16oB3on9wV8bql3nKVxBSHf_3FyfkJecVZzxuXbfT2OaGtR7jUbat7JJ2THmWKV4Kx9SnaMMVkJxb9dkMuU9oxx3kr1nFyIvhs4V_2O_LqBAGiyj4HGie7XIwQ_A0Xjwxjvaca4ZuoA_REcnTAeqMVTXBAS4PZ0_yMWPB4Nekh0PFEfMpqlBHIMYOZiMCEtswn58Zc_tAn0O2DRwTynF-TZZOYELx_OK_L144cv17fV3eebT9fv7yoreZOrXjnVSDXJMruEnsPAWG8tt72y0vVcyXESplOyaZgZO3CdVK1wTKhWjp1tmivy5uxdMP5cIWV98GmbwASIa9J8aIRoi2D4D5Srtik7bQsqzqjFmBLCpBf0B4MnzZneqtJ7vVWlt6o0G3SpqoReP_jX8QDuMfK3mwK8OwNQFnL0gDpZD8GC8wg2axf9v_y_AZtzp5Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1819430014</pqid></control><display><type>article</type><title>Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Lee, Seungki ; Katayama, Naoto ; Yoshizaki, Goro</creator><creatorcontrib>Lee, Seungki ; Katayama, Naoto ; Yoshizaki, Goro</creatorcontrib><description>Cryopreservation of fish sperm offers the practical applications in the selective breeding and biodiversity conservation. However, because of the lack of cryopreservation methods for fish eggs and embryos, maternally inherited cytoplasmic compartments cannot be successfully preserved. We previously developed an alternative method to derive functional eggs and sperm from cryopreserved whole testis by transplanting testicular cells into female and male recipients. However, if target fish had ovaries, the previous method employing male-derived germ cells would be ineffective. Here, we aimed to generate functional gametes from cryopreserved whole ovaries by transplanting ovarian germ cells into peritoneal cavity of sterile hatchlings. Cryopreservation conditions for rainbow trout ovaries (1.0 M DMSO, 0.1 M trehalose, and 10% egg yolk) were optimized by testing several different cryoprotective agents. Ovarian germ cells from thawed ovaries were intraperitoneally transplanted into allogeneic triploid hatchlings. Transplanted germ cells migrated toward and were incorporated into recipient gonads, where they underwent gametogenesis. Transplantation efficiency of ovarian germ cells remained stable after cryopreservation period up to 1185 days. Although all triploid recipients that did not undergo transplantation were functionally sterile, 5 of 25 female recipients and 7 of 25 male recipients reached sexual maturity at 2.5 years post-transplantation. Inseminating the resultant eggs and sperm generated viable offspring displaying the donor characteristics of orange body color, green fluorescence, and chromosome numbers. This method is thus a breakthrough tool for the conservation of endangered fish species that are crucial to cryopreserve the genetic resources of female fish. •No methods are currently available for cryopreserving fish eggs and embryos.•Rainbow trout ovaries were cryopreserved for up to 1185 days.•Germ cells recovered from thawed ovaries were transplanted into sterile recipients.•Transplanted ovarian germ cells differentiated into functional eggs and sperm.•This method is an effective means to preserve the fish genetic resources.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2016.08.156</identifier><identifier>PMID: 27581197</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Survival ; Cryopreservation ; Female ; Freezing ; Germ cell transplantation ; Germ Cells - transplantation ; Injections, Intraperitoneal ; Male ; Oncorhynchus mykiss ; Oncorhynchus mykiss - embryology ; Oogonial stem cells ; Ovary - cytology ; Ovary - physiology ; Ovary cryopreservation ; Rainbow trout ; Triploidy</subject><ispartof>Biochemical and biophysical research communications, 2016-09, Vol.478 (3), p.1478-1483</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c613t-79d9369f61976e71e8007cc1c79c6d7196bf2a596330ab5ed56942d02946b5c33</citedby><cites>FETCH-LOGICAL-c613t-79d9369f61976e71e8007cc1c79c6d7196bf2a596330ab5ed56942d02946b5c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2016.08.156$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27581197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Seungki</creatorcontrib><creatorcontrib>Katayama, Naoto</creatorcontrib><creatorcontrib>Yoshizaki, Goro</creatorcontrib><title>Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Cryopreservation of fish sperm offers the practical applications in the selective breeding and biodiversity conservation. However, because of the lack of cryopreservation methods for fish eggs and embryos, maternally inherited cytoplasmic compartments cannot be successfully preserved. We previously developed an alternative method to derive functional eggs and sperm from cryopreserved whole testis by transplanting testicular cells into female and male recipients. However, if target fish had ovaries, the previous method employing male-derived germ cells would be ineffective. Here, we aimed to generate functional gametes from cryopreserved whole ovaries by transplanting ovarian germ cells into peritoneal cavity of sterile hatchlings. Cryopreservation conditions for rainbow trout ovaries (1.0 M DMSO, 0.1 M trehalose, and 10% egg yolk) were optimized by testing several different cryoprotective agents. Ovarian germ cells from thawed ovaries were intraperitoneally transplanted into allogeneic triploid hatchlings. Transplanted germ cells migrated toward and were incorporated into recipient gonads, where they underwent gametogenesis. Transplantation efficiency of ovarian germ cells remained stable after cryopreservation period up to 1185 days. Although all triploid recipients that did not undergo transplantation were functionally sterile, 5 of 25 female recipients and 7 of 25 male recipients reached sexual maturity at 2.5 years post-transplantation. Inseminating the resultant eggs and sperm generated viable offspring displaying the donor characteristics of orange body color, green fluorescence, and chromosome numbers. This method is thus a breakthrough tool for the conservation of endangered fish species that are crucial to cryopreserve the genetic resources of female fish. •No methods are currently available for cryopreserving fish eggs and embryos.•Rainbow trout ovaries were cryopreserved for up to 1185 days.•Germ cells recovered from thawed ovaries were transplanted into sterile recipients.•Transplanted ovarian germ cells differentiated into functional eggs and sperm.•This method is an effective means to preserve the fish genetic resources.</description><subject>Animals</subject><subject>Cell Survival</subject><subject>Cryopreservation</subject><subject>Female</subject><subject>Freezing</subject><subject>Germ cell transplantation</subject><subject>Germ Cells - transplantation</subject><subject>Injections, Intraperitoneal</subject><subject>Male</subject><subject>Oncorhynchus mykiss</subject><subject>Oncorhynchus mykiss - embryology</subject><subject>Oogonial stem cells</subject><subject>Ovary - cytology</subject><subject>Ovary - physiology</subject><subject>Ovary cryopreservation</subject><subject>Rainbow trout</subject><subject>Triploidy</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcGO1SAUhonROHdGX8CFYemmFWhLS-LGTHTGZBI3mrgjFE6Vm16oB3on9wV8bql3nKVxBSHf_3FyfkJecVZzxuXbfT2OaGtR7jUbat7JJ2THmWKV4Kx9SnaMMVkJxb9dkMuU9oxx3kr1nFyIvhs4V_2O_LqBAGiyj4HGie7XIwQ_A0Xjwxjvaca4ZuoA_REcnTAeqMVTXBAS4PZ0_yMWPB4Nekh0PFEfMpqlBHIMYOZiMCEtswn58Zc_tAn0O2DRwTynF-TZZOYELx_OK_L144cv17fV3eebT9fv7yoreZOrXjnVSDXJMruEnsPAWG8tt72y0vVcyXESplOyaZgZO3CdVK1wTKhWjp1tmivy5uxdMP5cIWV98GmbwASIa9J8aIRoi2D4D5Srtik7bQsqzqjFmBLCpBf0B4MnzZneqtJ7vVWlt6o0G3SpqoReP_jX8QDuMfK3mwK8OwNQFnL0gDpZD8GC8wg2axf9v_y_AZtzp5Q</recordid><startdate>20160923</startdate><enddate>20160923</enddate><creator>Lee, Seungki</creator><creator>Katayama, Naoto</creator><creator>Yoshizaki, Goro</creator><general>Elsevier Inc</general><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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20160923</creationdate><title>Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells</title><author>Lee, Seungki ; Katayama, Naoto ; Yoshizaki, Goro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c613t-79d9369f61976e71e8007cc1c79c6d7196bf2a596330ab5ed56942d02946b5c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cell Survival</topic><topic>Cryopreservation</topic><topic>Female</topic><topic>Freezing</topic><topic>Germ cell transplantation</topic><topic>Germ Cells - transplantation</topic><topic>Injections, Intraperitoneal</topic><topic>Male</topic><topic>Oncorhynchus mykiss</topic><topic>Oncorhynchus mykiss - embryology</topic><topic>Oogonial stem cells</topic><topic>Ovary - cytology</topic><topic>Ovary - physiology</topic><topic>Ovary cryopreservation</topic><topic>Rainbow trout</topic><topic>Triploidy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Seungki</creatorcontrib><creatorcontrib>Katayama, Naoto</creatorcontrib><creatorcontrib>Yoshizaki, Goro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Seungki</au><au>Katayama, Naoto</au><au>Yoshizaki, Goro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2016-09-23</date><risdate>2016</risdate><volume>478</volume><issue>3</issue><spage>1478</spage><epage>1483</epage><pages>1478-1483</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Cryopreservation of fish sperm offers the practical applications in the selective breeding and biodiversity conservation. However, because of the lack of cryopreservation methods for fish eggs and embryos, maternally inherited cytoplasmic compartments cannot be successfully preserved. We previously developed an alternative method to derive functional eggs and sperm from cryopreserved whole testis by transplanting testicular cells into female and male recipients. However, if target fish had ovaries, the previous method employing male-derived germ cells would be ineffective. Here, we aimed to generate functional gametes from cryopreserved whole ovaries by transplanting ovarian germ cells into peritoneal cavity of sterile hatchlings. Cryopreservation conditions for rainbow trout ovaries (1.0 M DMSO, 0.1 M trehalose, and 10% egg yolk) were optimized by testing several different cryoprotective agents. Ovarian germ cells from thawed ovaries were intraperitoneally transplanted into allogeneic triploid hatchlings. Transplanted germ cells migrated toward and were incorporated into recipient gonads, where they underwent gametogenesis. Transplantation efficiency of ovarian germ cells remained stable after cryopreservation period up to 1185 days. Although all triploid recipients that did not undergo transplantation were functionally sterile, 5 of 25 female recipients and 7 of 25 male recipients reached sexual maturity at 2.5 years post-transplantation. Inseminating the resultant eggs and sperm generated viable offspring displaying the donor characteristics of orange body color, green fluorescence, and chromosome numbers. This method is thus a breakthrough tool for the conservation of endangered fish species that are crucial to cryopreserve the genetic resources of female fish. •No methods are currently available for cryopreserving fish eggs and embryos.•Rainbow trout ovaries were cryopreserved for up to 1185 days.•Germ cells recovered from thawed ovaries were transplanted into sterile recipients.•Transplanted ovarian germ cells differentiated into functional eggs and sperm.•This method is an effective means to preserve the fish genetic resources.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27581197</pmid><doi>10.1016/j.bbrc.2016.08.156</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0006-291X
ispartof Biochemical and biophysical research communications, 2016-09, Vol.478 (3), p.1478-1483
issn 0006-291X
1090-2104
language eng
recordid cdi_proquest_miscellaneous_1832245968
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Animals
Cell Survival
Cryopreservation
Female
Freezing
Germ cell transplantation
Germ Cells - transplantation
Injections, Intraperitoneal
Male
Oncorhynchus mykiss
Oncorhynchus mykiss - embryology
Oogonial stem cells
Ovary - cytology
Ovary - physiology
Ovary cryopreservation
Rainbow trout
Triploidy
title Generation of juvenile rainbow trout derived from cryopreserved whole ovaries by intraperitoneal transplantation of ovarian germ cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T03%3A52%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Generation%20of%20juvenile%20rainbow%20trout%20derived%20from%20cryopreserved%20whole%20ovaries%20by%20intraperitoneal%20transplantation%20of%20ovarian%20germ%20cells&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Lee,%20Seungki&rft.date=2016-09-23&rft.volume=478&rft.issue=3&rft.spage=1478&rft.epage=1483&rft.pages=1478-1483&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2016.08.156&rft_dat=%3Cproquest_cross%3E1819430014%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1819430014&rft_id=info:pmid/27581197&rft_els_id=S0006291X16314206&rfr_iscdi=true