Birth of piglets by in vitro fertilization of zona-free porcine oocytes
The present experiments were conducted to optimize in vitro fertilization conditions for zona pellucida-free (ZP-free) oocytes and their subsequent development. The results demonstrated that: (1) maximal fertilization efficiency was achieved at 200 spermatozoa per ZP-free oocyte. At this sperm dose,...
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Veröffentlicht in: | Theriogenology 2004-11, Vol.62 (8), p.1544-1556 |
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creator | Wu, Guang-Ming Lai, Liangxue Mao, Jiude McCauley, Tod C. Caamaño, Jose N. Cantley, Tom Rieke, August Murphy, Clifton N. Prather, Randall S. Didion, Brad A. Day, Billy N. |
description | The present experiments were conducted to optimize in vitro fertilization conditions for zona pellucida-free (ZP-free) oocytes and their subsequent development. The results demonstrated that: (1) maximal fertilization efficiency was achieved at 200 spermatozoa per ZP-free oocyte. At this sperm dose, there were no significant differences in penetration rates and polyspermy rates from controls (zona-intact oocytes with 1000 spermatozoa/oocyte), indicating that ZPs of in vitro matured pig oocytes failed to block polyspermy during in vitro fertilization. (2) In vitro development of zygotes from ZP-free oocytes showed that there was no difference in cleavage rates. The blastocyst rate was slightly lower in the ZP-free group than the control. However, there was no difference in cell number per blastocyst between the control and the ZP-free group. (3) Examination of acrosome status by a specific fluorescein isothiocyanate-conjugated peanut agglutinin (FITC-PNA) staining procedure revealed that frozen–thawed pig spermatozoa could undergo acrosome reaction and penetrate oocytes without induction by ZP. These data suggested that there are alternative mechanistic pathways for acrosome reaction induction during the fertilization process than the widely accepted sperm–zona receptor models. Finally, the viability of ZP-free derived embryos was demonstrated by full-term development and the delivery of healthy piglets following embryo transfer. In conclusion, the present experiments showed for the first time in farm animals, that normal embryos could be produced by in vitro fertilization of ZP-free oocytes in optimized conditions and that they could develop normally to full-term. |
doi_str_mv | 10.1016/j.theriogenology.2004.02.016 |
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The results demonstrated that: (1) maximal fertilization efficiency was achieved at 200 spermatozoa per ZP-free oocyte. At this sperm dose, there were no significant differences in penetration rates and polyspermy rates from controls (zona-intact oocytes with 1000 spermatozoa/oocyte), indicating that ZPs of in vitro matured pig oocytes failed to block polyspermy during in vitro fertilization. (2) In vitro development of zygotes from ZP-free oocytes showed that there was no difference in cleavage rates. The blastocyst rate was slightly lower in the ZP-free group than the control. However, there was no difference in cell number per blastocyst between the control and the ZP-free group. (3) Examination of acrosome status by a specific fluorescein isothiocyanate-conjugated peanut agglutinin (FITC-PNA) staining procedure revealed that frozen–thawed pig spermatozoa could undergo acrosome reaction and penetrate oocytes without induction by ZP. These data suggested that there are alternative mechanistic pathways for acrosome reaction induction during the fertilization process than the widely accepted sperm–zona receptor models. Finally, the viability of ZP-free derived embryos was demonstrated by full-term development and the delivery of healthy piglets following embryo transfer. In conclusion, the present experiments showed for the first time in farm animals, that normal embryos could be produced by in vitro fertilization of ZP-free oocytes in optimized conditions and that they could develop normally to full-term.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2004.02.016</identifier><identifier>PMID: 15451262</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acrosome Reaction ; Animals ; Cleavage Stage, Ovum ; Cryopreservation - veterinary ; Development ; Embryo Culture Techniques - veterinary ; Embryo Transfer - veterinary ; Embryonic Development ; Embryos ; Female ; Fertilization in Vitro - methods ; Fertilization in Vitro - veterinary ; In vitro fertilization ; Male ; Microscopy, Fluorescence ; Oocytes ; Oocytes - physiology ; Porcine ; Pregnancy ; Pregnancy Outcome ; Semen Preservation - veterinary ; Sperm-Ovum Interactions ; Swine ; Zona Pellucida - physiology</subject><ispartof>Theriogenology, 2004-11, Vol.62 (8), p.1544-1556</ispartof><rights>2004 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-6b87ac883aecae1854967da3a274c932ce2cfc8889b8aafe6e7f2d5ef3a126973</citedby><cites>FETCH-LOGICAL-c448t-6b87ac883aecae1854967da3a274c932ce2cfc8889b8aafe6e7f2d5ef3a126973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0093691X04001153$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15451262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Guang-Ming</creatorcontrib><creatorcontrib>Lai, Liangxue</creatorcontrib><creatorcontrib>Mao, Jiude</creatorcontrib><creatorcontrib>McCauley, Tod C.</creatorcontrib><creatorcontrib>Caamaño, Jose N.</creatorcontrib><creatorcontrib>Cantley, Tom</creatorcontrib><creatorcontrib>Rieke, August</creatorcontrib><creatorcontrib>Murphy, Clifton N.</creatorcontrib><creatorcontrib>Prather, Randall S.</creatorcontrib><creatorcontrib>Didion, Brad A.</creatorcontrib><creatorcontrib>Day, Billy N.</creatorcontrib><title>Birth of piglets by in vitro fertilization of zona-free porcine oocytes</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>The present experiments were conducted to optimize in vitro fertilization conditions for zona pellucida-free (ZP-free) oocytes and their subsequent development. The results demonstrated that: (1) maximal fertilization efficiency was achieved at 200 spermatozoa per ZP-free oocyte. At this sperm dose, there were no significant differences in penetration rates and polyspermy rates from controls (zona-intact oocytes with 1000 spermatozoa/oocyte), indicating that ZPs of in vitro matured pig oocytes failed to block polyspermy during in vitro fertilization. (2) In vitro development of zygotes from ZP-free oocytes showed that there was no difference in cleavage rates. The blastocyst rate was slightly lower in the ZP-free group than the control. However, there was no difference in cell number per blastocyst between the control and the ZP-free group. (3) Examination of acrosome status by a specific fluorescein isothiocyanate-conjugated peanut agglutinin (FITC-PNA) staining procedure revealed that frozen–thawed pig spermatozoa could undergo acrosome reaction and penetrate oocytes without induction by ZP. These data suggested that there are alternative mechanistic pathways for acrosome reaction induction during the fertilization process than the widely accepted sperm–zona receptor models. Finally, the viability of ZP-free derived embryos was demonstrated by full-term development and the delivery of healthy piglets following embryo transfer. In conclusion, the present experiments showed for the first time in farm animals, that normal embryos could be produced by in vitro fertilization of ZP-free oocytes in optimized conditions and that they could develop normally to full-term.</description><subject>Acrosome Reaction</subject><subject>Animals</subject><subject>Cleavage Stage, Ovum</subject><subject>Cryopreservation - veterinary</subject><subject>Development</subject><subject>Embryo Culture Techniques - veterinary</subject><subject>Embryo Transfer - veterinary</subject><subject>Embryonic Development</subject><subject>Embryos</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Fertilization in Vitro - veterinary</subject><subject>In vitro fertilization</subject><subject>Male</subject><subject>Microscopy, Fluorescence</subject><subject>Oocytes</subject><subject>Oocytes - physiology</subject><subject>Porcine</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Semen Preservation - veterinary</subject><subject>Sperm-Ovum Interactions</subject><subject>Swine</subject><subject>Zona Pellucida - physiology</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE9LAzEQxYMotla_guxBvO2aP9tsFrxosVUoeFHwFtLspE3ZbtYkLWw_vVtaEG-e5vB-b97MQ-iO4Ixgwh_WWVyBt24JjavdsssoxnmGadaLZ2hIRFGmjDJyjoYYlyzlJfkaoKsQ1hhjxjm5RAMyzseEcjpEs2fr4ypxJmntsoYYkkWX2CbZ2ehdYsBHW9u9itY1B2jvGpUaD5C0zmvbQOKc7iKEa3RhVB3g5jRH6HP68jF5Tefvs7fJ0zzVeS5iyheiUFoIpkArIGKcl7yoFFO0yHXJqAaqTa-LciGUMsChMLQag2Gqv7cs2AjdH_e23n1vIUS5sUFDXasG3DZIzkuKCy568PEIau9C8GBk6-1G-U4SLA9FyrX8W6Q8FCkxlb3Y229POdvFBqpf86m5HpgeAei_3VnwMmgLjYbKetBRVs7-L-kHMkWO5A</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Wu, Guang-Ming</creator><creator>Lai, Liangxue</creator><creator>Mao, Jiude</creator><creator>McCauley, Tod C.</creator><creator>Caamaño, Jose N.</creator><creator>Cantley, Tom</creator><creator>Rieke, August</creator><creator>Murphy, Clifton N.</creator><creator>Prather, Randall S.</creator><creator>Didion, Brad A.</creator><creator>Day, Billy N.</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></search><sort><creationdate>20041101</creationdate><title>Birth of piglets by in vitro fertilization of zona-free porcine oocytes</title><author>Wu, Guang-Ming ; Lai, Liangxue ; Mao, Jiude ; McCauley, Tod C. ; Caamaño, Jose N. ; Cantley, Tom ; Rieke, August ; Murphy, Clifton N. ; Prather, Randall S. ; Didion, Brad A. ; Day, Billy N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-6b87ac883aecae1854967da3a274c932ce2cfc8889b8aafe6e7f2d5ef3a126973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Acrosome Reaction</topic><topic>Animals</topic><topic>Cleavage Stage, Ovum</topic><topic>Cryopreservation - veterinary</topic><topic>Development</topic><topic>Embryo Culture Techniques - veterinary</topic><topic>Embryo Transfer - veterinary</topic><topic>Embryonic Development</topic><topic>Embryos</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Fertilization in Vitro - veterinary</topic><topic>In vitro fertilization</topic><topic>Male</topic><topic>Microscopy, Fluorescence</topic><topic>Oocytes</topic><topic>Oocytes - physiology</topic><topic>Porcine</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Semen Preservation - veterinary</topic><topic>Sperm-Ovum Interactions</topic><topic>Swine</topic><topic>Zona Pellucida - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Guang-Ming</creatorcontrib><creatorcontrib>Lai, Liangxue</creatorcontrib><creatorcontrib>Mao, Jiude</creatorcontrib><creatorcontrib>McCauley, Tod C.</creatorcontrib><creatorcontrib>Caamaño, Jose N.</creatorcontrib><creatorcontrib>Cantley, Tom</creatorcontrib><creatorcontrib>Rieke, August</creatorcontrib><creatorcontrib>Murphy, Clifton N.</creatorcontrib><creatorcontrib>Prather, Randall S.</creatorcontrib><creatorcontrib>Didion, Brad A.</creatorcontrib><creatorcontrib>Day, Billy N.</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><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Guang-Ming</au><au>Lai, Liangxue</au><au>Mao, Jiude</au><au>McCauley, Tod C.</au><au>Caamaño, Jose N.</au><au>Cantley, Tom</au><au>Rieke, August</au><au>Murphy, Clifton N.</au><au>Prather, Randall S.</au><au>Didion, Brad A.</au><au>Day, Billy N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Birth of piglets by in vitro fertilization of zona-free porcine oocytes</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>62</volume><issue>8</issue><spage>1544</spage><epage>1556</epage><pages>1544-1556</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>The present experiments were conducted to optimize in vitro fertilization conditions for zona pellucida-free (ZP-free) oocytes and their subsequent development. The results demonstrated that: (1) maximal fertilization efficiency was achieved at 200 spermatozoa per ZP-free oocyte. At this sperm dose, there were no significant differences in penetration rates and polyspermy rates from controls (zona-intact oocytes with 1000 spermatozoa/oocyte), indicating that ZPs of in vitro matured pig oocytes failed to block polyspermy during in vitro fertilization. (2) In vitro development of zygotes from ZP-free oocytes showed that there was no difference in cleavage rates. The blastocyst rate was slightly lower in the ZP-free group than the control. However, there was no difference in cell number per blastocyst between the control and the ZP-free group. (3) Examination of acrosome status by a specific fluorescein isothiocyanate-conjugated peanut agglutinin (FITC-PNA) staining procedure revealed that frozen–thawed pig spermatozoa could undergo acrosome reaction and penetrate oocytes without induction by ZP. These data suggested that there are alternative mechanistic pathways for acrosome reaction induction during the fertilization process than the widely accepted sperm–zona receptor models. Finally, the viability of ZP-free derived embryos was demonstrated by full-term development and the delivery of healthy piglets following embryo transfer. In conclusion, the present experiments showed for the first time in farm animals, that normal embryos could be produced by in vitro fertilization of ZP-free oocytes in optimized conditions and that they could develop normally to full-term.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15451262</pmid><doi>10.1016/j.theriogenology.2004.02.016</doi><tpages>13</tpages></addata></record> |
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subjects | Acrosome Reaction Animals Cleavage Stage, Ovum Cryopreservation - veterinary Development Embryo Culture Techniques - veterinary Embryo Transfer - veterinary Embryonic Development Embryos Female Fertilization in Vitro - methods Fertilization in Vitro - veterinary In vitro fertilization Male Microscopy, Fluorescence Oocytes Oocytes - physiology Porcine Pregnancy Pregnancy Outcome Semen Preservation - veterinary Sperm-Ovum Interactions Swine Zona Pellucida - physiology |
title | Birth of piglets by in vitro fertilization of zona-free porcine oocytes |
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