Vitrification of Fully Grown and Growing Porcine Oocytes Using Germinal Vesicle Transfer
The survival rate of vitrified germinal vesicle (GV) stage porcine oocytes is very low, and it is not known if the vitrification damages the nucleus, cytoplasm or both. We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of no...
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Veröffentlicht in: | Journal of Reproduction and Development 2011, Vol.57(3), pp.335-341 |
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description | The survival rate of vitrified germinal vesicle (GV) stage porcine oocytes is very low, and it is not known if the vitrification damages the nucleus, cytoplasm or both. We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of nonvitrified FG cumulus-denuded oocytes reached the metaphase II (MII) stage in culture. When growing oocytes from preantral (PA) and early antral (EA) follicles were matured in vitro, almost all oocytes were arrested at the GV stage (GV stage: PA 88.9 and EA 79.5%, respectively). When fresh GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes and matured in vitro, some of them reached the MII stage (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). The maturation rate of vitrified FG oocytes was only 6.1% but increased dramatically when vitrified GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes (MII stage: VitFG/FG 43.9%, VitPA/FG 7.1% and VitEA/FG 26.3%, respectively). These results were not significantly different from those for the nonvitrified groups (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). We activated the reconstructed oocytes that received fresh or vitrified GVs (FG/FG, EA/FG, VitFG/FG and VitEA/FG) and examined their embryonic development. Cleaved embryos (nonvitrified groups 13.0-61.8%, vitrified groups 33.3-40.0%) and blastocysts (nonvitrified groups 0.0-18.2%, vitrified groups 0.0-2.9%) were obtained after activation. These results demonstrate that vitrified porcine GVs maintain maturational and developmental competence and that vitrification predominantly damages the cytoplasm. |
doi_str_mv | 10.1262/jrd.10-177H |
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We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of nonvitrified FG cumulus-denuded oocytes reached the metaphase II (MII) stage in culture. When growing oocytes from preantral (PA) and early antral (EA) follicles were matured in vitro, almost all oocytes were arrested at the GV stage (GV stage: PA 88.9 and EA 79.5%, respectively). When fresh GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes and matured in vitro, some of them reached the MII stage (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). The maturation rate of vitrified FG oocytes was only 6.1% but increased dramatically when vitrified GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes (MII stage: VitFG/FG 43.9%, VitPA/FG 7.1% and VitEA/FG 26.3%, respectively). These results were not significantly different from those for the nonvitrified groups (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). We activated the reconstructed oocytes that received fresh or vitrified GVs (FG/FG, EA/FG, VitFG/FG and VitEA/FG) and examined their embryonic development. Cleaved embryos (nonvitrified groups 13.0-61.8%, vitrified groups 33.3-40.0%) and blastocysts (nonvitrified groups 0.0-18.2%, vitrified groups 0.0-2.9%) were obtained after activation. These results demonstrate that vitrified porcine GVs maintain maturational and developmental competence and that vitrification predominantly damages the cytoplasm.</description><identifier>ISSN: 0916-8818</identifier><identifier>EISSN: 1348-4400</identifier><identifier>DOI: 10.1262/jrd.10-177H</identifier><identifier>PMID: 21289465</identifier><language>eng</language><publisher>Japan: THE SOCIETY FOR REPRODUCTION AND DEVELOPMENT</publisher><subject>Animals ; Blastocyst - drug effects ; Cells, Cultured ; Cryoprotective Agents - pharmacology ; Female ; Germinal vesicle (GV) stage oocyte ; Germinal vesicle (GV) transfer ; Oocytes ; Pig ; Swine ; Vitrification</subject><ispartof>Journal of Reproduction and Development, 2011, Vol.57(3), pp.335-341</ispartof><rights>2011 Society for Reproduction and Development</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-f5d2643a50111108676dca71c222d7f696fc470ee7e6e92d8c1c801eaf3da2be3</citedby><cites>FETCH-LOGICAL-c524t-f5d2643a50111108676dca71c222d7f696fc470ee7e6e92d8c1c801eaf3da2be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21289465$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NAKAGAWA, Shoma</creatorcontrib><creatorcontrib>MAEDOMARI, Naoki</creatorcontrib><creatorcontrib>KIKUCHI, Kazuhiro</creatorcontrib><creatorcontrib>NAGAI, Takashi</creatorcontrib><creatorcontrib>MIYANO, Takashi</creatorcontrib><creatorcontrib>JR, Josef FULKA</creatorcontrib><creatorcontrib>MANABE, Noboru</creatorcontrib><title>Vitrification of Fully Grown and Growing Porcine Oocytes Using Germinal Vesicle Transfer</title><title>Journal of Reproduction and Development</title><addtitle>J. Reprod. Dev.</addtitle><description>The survival rate of vitrified germinal vesicle (GV) stage porcine oocytes is very low, and it is not known if the vitrification damages the nucleus, cytoplasm or both. We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of nonvitrified FG cumulus-denuded oocytes reached the metaphase II (MII) stage in culture. When growing oocytes from preantral (PA) and early antral (EA) follicles were matured in vitro, almost all oocytes were arrested at the GV stage (GV stage: PA 88.9 and EA 79.5%, respectively). When fresh GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes and matured in vitro, some of them reached the MII stage (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). The maturation rate of vitrified FG oocytes was only 6.1% but increased dramatically when vitrified GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes (MII stage: VitFG/FG 43.9%, VitPA/FG 7.1% and VitEA/FG 26.3%, respectively). These results were not significantly different from those for the nonvitrified groups (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). We activated the reconstructed oocytes that received fresh or vitrified GVs (FG/FG, EA/FG, VitFG/FG and VitEA/FG) and examined their embryonic development. Cleaved embryos (nonvitrified groups 13.0-61.8%, vitrified groups 33.3-40.0%) and blastocysts (nonvitrified groups 0.0-18.2%, vitrified groups 0.0-2.9%) were obtained after activation. These results demonstrate that vitrified porcine GVs maintain maturational and developmental competence and that vitrification predominantly damages the cytoplasm.</description><subject>Animals</subject><subject>Blastocyst - drug effects</subject><subject>Cells, Cultured</subject><subject>Cryoprotective Agents - pharmacology</subject><subject>Female</subject><subject>Germinal vesicle (GV) stage oocyte</subject><subject>Germinal vesicle (GV) transfer</subject><subject>Oocytes</subject><subject>Pig</subject><subject>Swine</subject><subject>Vitrification</subject><issn>0916-8818</issn><issn>1348-4400</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEFrAjEQhUNpqdb21HvJvaxNstkkexSpWhDsQaW3JWYnNrJmJdlS_PfdVescZh4zHw_mIfRMyZAywd52oRxSklApZzeoT1OuEs4JuUV9klORKEVVDz3EuCMkZZng96jHKFM5F1kffa1dE5x1Rjeu9ri2ePJTVUc8DfWvx9qXJ-X8Fn_WwTgPeFGbYwMRr2K3nULYO68rvIboTAV4GbSPFsIjurO6ivB0mQO0mrwvx7Nkvph-jEfzxGSMN4nNSiZ4qjNC2yJKSFEaLalhjJXSilxYwyUBkCAgZ6Uy1ChCQdu01GwD6QC9nn1NqGMMYItDcHsdjgUlRZdP0eZz0m0-Lf1ypg8_mz2UV_Y_kBYYnYFdbPQWroAOTffeySyTRdq1i-n1Zr51KMCnf7vXeUA</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>NAKAGAWA, Shoma</creator><creator>MAEDOMARI, Naoki</creator><creator>KIKUCHI, Kazuhiro</creator><creator>NAGAI, Takashi</creator><creator>MIYANO, Takashi</creator><creator>JR, Josef FULKA</creator><creator>MANABE, Noboru</creator><general>THE SOCIETY FOR REPRODUCTION AND DEVELOPMENT</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></search><sort><creationdate>20110601</creationdate><title>Vitrification of Fully Grown and Growing Porcine Oocytes Using Germinal Vesicle Transfer</title><author>NAKAGAWA, Shoma ; MAEDOMARI, Naoki ; KIKUCHI, Kazuhiro ; NAGAI, Takashi ; MIYANO, Takashi ; JR, Josef FULKA ; MANABE, Noboru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-f5d2643a50111108676dca71c222d7f696fc470ee7e6e92d8c1c801eaf3da2be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Blastocyst - drug effects</topic><topic>Cells, Cultured</topic><topic>Cryoprotective Agents - pharmacology</topic><topic>Female</topic><topic>Germinal vesicle (GV) stage oocyte</topic><topic>Germinal vesicle (GV) transfer</topic><topic>Oocytes</topic><topic>Pig</topic><topic>Swine</topic><topic>Vitrification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NAKAGAWA, Shoma</creatorcontrib><creatorcontrib>MAEDOMARI, Naoki</creatorcontrib><creatorcontrib>KIKUCHI, Kazuhiro</creatorcontrib><creatorcontrib>NAGAI, Takashi</creatorcontrib><creatorcontrib>MIYANO, Takashi</creatorcontrib><creatorcontrib>JR, Josef FULKA</creatorcontrib><creatorcontrib>MANABE, Noboru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of Reproduction and Development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NAKAGAWA, Shoma</au><au>MAEDOMARI, Naoki</au><au>KIKUCHI, Kazuhiro</au><au>NAGAI, Takashi</au><au>MIYANO, Takashi</au><au>JR, Josef FULKA</au><au>MANABE, Noboru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vitrification of Fully Grown and Growing Porcine Oocytes Using Germinal Vesicle Transfer</atitle><jtitle>Journal of Reproduction and Development</jtitle><addtitle>J. Reprod. Dev.</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>57</volume><issue>3</issue><spage>335</spage><epage>341</epage><pages>335-341</pages><issn>0916-8818</issn><eissn>1348-4400</eissn><abstract>The survival rate of vitrified germinal vesicle (GV) stage porcine oocytes is very low, and it is not known if the vitrification damages the nucleus, cytoplasm or both. We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of nonvitrified FG cumulus-denuded oocytes reached the metaphase II (MII) stage in culture. When growing oocytes from preantral (PA) and early antral (EA) follicles were matured in vitro, almost all oocytes were arrested at the GV stage (GV stage: PA 88.9 and EA 79.5%, respectively). When fresh GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes and matured in vitro, some of them reached the MII stage (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). The maturation rate of vitrified FG oocytes was only 6.1% but increased dramatically when vitrified GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes (MII stage: VitFG/FG 43.9%, VitPA/FG 7.1% and VitEA/FG 26.3%, respectively). These results were not significantly different from those for the nonvitrified groups (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). We activated the reconstructed oocytes that received fresh or vitrified GVs (FG/FG, EA/FG, VitFG/FG and VitEA/FG) and examined their embryonic development. Cleaved embryos (nonvitrified groups 13.0-61.8%, vitrified groups 33.3-40.0%) and blastocysts (nonvitrified groups 0.0-18.2%, vitrified groups 0.0-2.9%) were obtained after activation. These results demonstrate that vitrified porcine GVs maintain maturational and developmental competence and that vitrification predominantly damages the cytoplasm.</abstract><cop>Japan</cop><pub>THE SOCIETY FOR REPRODUCTION AND DEVELOPMENT</pub><pmid>21289465</pmid><doi>10.1262/jrd.10-177H</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blastocyst - drug effects Cells, Cultured Cryoprotective Agents - pharmacology Female Germinal vesicle (GV) stage oocyte Germinal vesicle (GV) transfer Oocytes Pig Swine Vitrification |
title | Vitrification of Fully Grown and Growing Porcine Oocytes Using Germinal Vesicle Transfer |
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