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
Hauptverfasser: 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.
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container_end_page 1556
container_issue 8
container_start_page 1544
container_title Theriogenology
container_volume 62
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. 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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. 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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.</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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