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Effects of the conditioned medium of mesenchymal stem cells on mouse oocyte activation and development
Feng, D. Q; Zhou, Y; Ling, B; Gao, T; Shi, Y. Y; Wei, H. M; Tian, Z. G.
  • Feng, D. Q; Anhui Medical University. Anhui Province Key Laboratory of Molecular Medicine. Hefei. CN
  • Zhou, Y; Anhui Medical University. Anhui Province Key Laboratory of Molecular Medicine. Hefei. CN
  • Ling, B; Anhui Medical University. Anhui Province Key Laboratory of Molecular Medicine. Hefei. CN
  • Gao, T; Anhui Medical University. Anhui Provincial Hospital. Department of Obstetrics and Gynecology. Hefei. CN
  • Shi, Y. Y; Anhui Medical University. Anhui Province Key Laboratory of Molecular Medicine. Hefei. CN
  • Wei, H. M; University of Science and Technology of China. Hefei National Laboratory for Physical Science at Microscale and School of Life Science. Institution of Immunology. Hefei. CN
  • Tian, Z. G; University of Science and Technology of China. Hefei National Laboratory for Physical Science at Microscale and School of Life Science. Institution of Immunology. Hefei. CN
Braz. j. med. biol. res ; 42(6): 506-514, June 2009. ilus, tab, graf
Article in English | LILACS | ID: lil-512771
ABSTRACT
Mesenchymal stem cells (MSCs) have been reported to secrete a variety of cytokines and growth factors acting as trophic suppliers, but little is known regarding the effects of conditioned medium (CM) of MSCs isolated from femurs and tibias of mouse on the artificial activation of mouse oocytes and on the developmental competence of the parthenotes. In the current study, we investigated the effect of CM on the events of mouse oocyte activation, namely oscillations of cytosolic calcium concentration ([Ca²+]i), meiosis resumption, pronucleus formation, and parthenogenetic development. The surface markers of MSCs were identified with a fluorescence-activated cell sorter. The dynamic changes of the spindle and formation of pronuclei were examined by laser-scanning confocal microscopy. Exposure of cumulus-oocyte complexes to CM for 40 min was optimal for inducing oocyte parthenogenetic activation and evoking [Ca²+]i oscillations similar to those evoked by sperm (95 vs 100 percent; P > 0.05). Parthenogenetically activated oocytes immediately treated with 7.5 µg/mL cytochalasin B (CB), which inhibited spindle rotation and second polar body extrusion, were mostly diploid (93 vs 6 percent, P < 0.01) while CB-untreated oocytes were mostly haploid (5 vs 83 percent, P < 0.01). Consequently, the blastocyst rate was higher in the CB-treated than in the CB-untreated oocytes. There was no significant difference in developmental rate between oocytes activated with CM and 7 percent ethanol (62 vs 62 percent, P > 0.05), but the developmental competence of the fertilized oocytes was superior to that of the parthenotes (88 vs 62 percent, P < 0.05). The present results demonstrate that CM can effectively activate mouse oocytes, as judged by the generation of [Ca²+]i oscillations, completion of meiosis and parthenogenetic development.
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Full text: Available Index: LILACS (Americas) Main subject: Oocytes / Parthenogenesis / Calcium / Culture Media, Conditioned / Cytochalasin B / Mesenchymal Stem Cells Type of study: Prognostic study Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2009 Type: Article / Project document Affiliation country: China Institution/Affiliation country: Anhui Medical University/CN / University of Science and Technology of China/CN

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Full text: Available Index: LILACS (Americas) Main subject: Oocytes / Parthenogenesis / Calcium / Culture Media, Conditioned / Cytochalasin B / Mesenchymal Stem Cells Type of study: Prognostic study Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2009 Type: Article / Project document Affiliation country: China Institution/Affiliation country: Anhui Medical University/CN / University of Science and Technology of China/CN