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Optimization of Ca2+ concentrations in fusion and activation media for production of cloned embryos from miniature pig somatic cells

The effects of Ca2+ concentration in activation medium and cytochalasin B treatment after activation on the parthenogenetic development of pig oocytes were examined. In addition, cloned embryos derived from miniature pig somatic cells were activated under optimal conditions and the effects of Ca2+ i...

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Published in:Journal of Reproduction and Development 2005, Vol.51(6), pp.699-706
Main Authors: Miyoshi, K.(Kagoshima Univ. (Japan). Faculty of Agriculture), Yuki, Y, Yoshida, M
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Language:English
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container_title Journal of Reproduction and Development
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creator Miyoshi, K.(Kagoshima Univ. (Japan). Faculty of Agriculture)
Yuki, Y
Yoshida, M
description The effects of Ca2+ concentration in activation medium and cytochalasin B treatment after activation on the parthenogenetic development of pig oocytes were examined. In addition, cloned embryos derived from miniature pig somatic cells were activated under optimal conditions and the effects of Ca2+ in fusion medium on the development of embryos after activation was examined. When oocytes were activated in 0.1 mM Ca2+ and then treated with cytochalasin B, the blastocyst formation rate (28.6%) was significantly higher than those activated in 0-0.05) or 1.0 mM (11.0-18.3%). Treatment with cytochalasin B decreased the second polar body extrusion rate of activated oocytes. The presence or absence of Ca2+ in fusion medium did not affect the fusion rate of miniature pig somatic cells with recipient oocytes. A few cloned embryos developed to the blastocyst stage (2.7-9.0%) without an additional activation treatment. On the other hand, significantly more embryos developed to the blastocyst stage after activation treatment when they were fused in the absence (28.9%) of Ca2+ rather than the presence (16.5%) of it. These results show that the highest blastocyst formation rate for miniature pig cloned embryos is obtained when donor cells and recipient oocytes are fused in the absence of Ca2+ and then activated in 0.1 mM Ca2+ and treated with cytochalasin B.
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(Japan). Faculty of Agriculture)</creatorcontrib><creatorcontrib>Yuki, Y</creatorcontrib><creatorcontrib>Yoshida, M</creatorcontrib><title>Optimization of Ca2+ concentrations in fusion and activation media for production of cloned embryos from miniature pig somatic cells</title><title>Journal of Reproduction and Development</title><addtitle>J. Reprod. Dev.</addtitle><description>The effects of Ca2+ concentration in activation medium and cytochalasin B treatment after activation on the parthenogenetic development of pig oocytes were examined. In addition, cloned embryos derived from miniature pig somatic cells were activated under optimal conditions and the effects of Ca2+ in fusion medium on the development of embryos after activation was examined. When oocytes were activated in 0.1 mM Ca2+ and then treated with cytochalasin B, the blastocyst formation rate (28.6%) was significantly higher than those activated in 0-0.05) or 1.0 mM (11.0-18.3%). 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Faculty of Agriculture) ; Yuki, Y ; Yoshida, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-b712f45882ecf851b02c91a884b3554c42c907dc3f152e36900230a5b1fb321a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Blastocyst - cytology</topic><topic>Ca2</topic><topic>CALCIO</topic><topic>CALCIUM</topic><topic>Calcium - pharmacology</topic><topic>Cell Fusion - methods</topic><topic>CELLS</topic><topic>Cells, Cultured</topic><topic>CELLULE</topic><topic>CELULAS</topic><topic>CERDO</topic><topic>Cloning, Organism - methods</topic><topic>CULTIVO IN VITRO</topic><topic>CULTURE IN VITRO</topic><topic>Cytochalasin B - pharmacology</topic><topic>DESARROLLO EMBRIONARIO</topic><topic>DEVELOPPEMENT EMBRYONNAIRE</topic><topic>Electric Stimulation</topic><topic>Embryo development</topic><topic>EMBRYONIC DEVELOPMENT</topic><topic>Female</topic><topic>IN VITRO CULTURE</topic><topic>ION</topic><topic>IONES</topic><topic>IONS</topic><topic>Miniature pig</topic><topic>NOYAU CELLULAIRE</topic><topic>Nuclear transfer</topic><topic>NUCLEO</topic><topic>NUCLEUS</topic><topic>Oocyte activation</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - physiology</topic><topic>OVA</topic><topic>OVULE</topic><topic>OVULO</topic><topic>Parthenogenesis</topic><topic>PORCIN</topic><topic>REPIQUAGE</topic><topic>SWINE</topic><topic>Swine, Miniature</topic><topic>TRANSPLANTING</topic><topic>TRASPLANTE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyoshi, K.(Kagoshima Univ. 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Reprod. Dev.</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>51</volume><issue>6</issue><spage>699</spage><epage>706</epage><pages>699-706</pages><issn>0916-8818</issn><eissn>1348-4400</eissn><abstract>The effects of Ca2+ concentration in activation medium and cytochalasin B treatment after activation on the parthenogenetic development of pig oocytes were examined. In addition, cloned embryos derived from miniature pig somatic cells were activated under optimal conditions and the effects of Ca2+ in fusion medium on the development of embryos after activation was examined. When oocytes were activated in 0.1 mM Ca2+ and then treated with cytochalasin B, the blastocyst formation rate (28.6%) was significantly higher than those activated in 0-0.05) or 1.0 mM (11.0-18.3%). Treatment with cytochalasin B decreased the second polar body extrusion rate of activated oocytes. The presence or absence of Ca2+ in fusion medium did not affect the fusion rate of miniature pig somatic cells with recipient oocytes. A few cloned embryos developed to the blastocyst stage (2.7-9.0%) without an additional activation treatment. On the other hand, significantly more embryos developed to the blastocyst stage after activation treatment when they were fused in the absence (28.9%) of Ca2+ rather than the presence (16.5%) of it. These results show that the highest blastocyst formation rate for miniature pig cloned embryos is obtained when donor cells and recipient oocytes are fused in the absence of Ca2+ and then activated in 0.1 mM Ca2+ and treated with cytochalasin B.</abstract><cop>Japan</cop><pub>THE SOCIETY FOR REPRODUCTION AND DEVELOPMENT</pub><pmid>16141644</pmid><doi>10.1262/jrd.17023</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Blastocyst - cytology
Ca2
CALCIO
CALCIUM
Calcium - pharmacology
Cell Fusion - methods
CELLS
Cells, Cultured
CELLULE
CELULAS
CERDO
Cloning, Organism - methods
CULTIVO IN VITRO
CULTURE IN VITRO
Cytochalasin B - pharmacology
DESARROLLO EMBRIONARIO
DEVELOPPEMENT EMBRYONNAIRE
Electric Stimulation
Embryo development
EMBRYONIC DEVELOPMENT
Female
IN VITRO CULTURE
ION
IONES
IONS
Miniature pig
NOYAU CELLULAIRE
Nuclear transfer
NUCLEO
NUCLEUS
Oocyte activation
Oocytes - drug effects
Oocytes - physiology
OVA
OVULE
OVULO
Parthenogenesis
PORCIN
REPIQUAGE
SWINE
Swine, Miniature
TRANSPLANTING
TRASPLANTE
title Optimization of Ca2+ concentrations in fusion and activation media for production of cloned embryos from miniature pig somatic cells
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