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Parthenogenetic activation of bovine oocytes using bovine and murine phospholipase C zeta

✍ Scribed by Pablo J Ross; Zeki Beyhan; Amy E Iager; Sook-Young Yoon; Christopher Malcuit; Karl Schellander; Rafael A Fissore; Jose B Cibelli


Book ID
104492685
Publisher
BioMed Central
Year
2008
Tongue
English
Weight
624 KB
Volume
8
Category
Article
ISSN
1471-213X

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✦ Synopsis


Background

During natural fertilization, sperm fusion with the oocyte induces long lasting intracellular calcium oscillations which in turn are responsible for oocyte activation. PLCZ1 has been identified as the factor that the sperm delivers into the egg to induce such a response. We tested the hypothesis that PLCZ1 cRNA injection can be used to activate bovine oocytes.

Results

Mouse and bovine PLCZ1 cRNAs were injected into matured bovine oocytes at different concentrations. Within the concentrations tested, mouse PLCZ1 injection activated bovine oocytes at a maximum rate when the pipette concentration of cRNA ranged from 0.25 to 1 ΞΌg/ΞΌL, while bovine PLCZ1 was optimal at 0.1 ΞΌg/ΞΌL. At their most effective concentrations, PLCZ1 induced parthenogenetic development at rates similar to those observed using other activation stimuli such as Ionomycin/CHX and Ionomycin/DMAP. Injection of mouse and bovine PLCZ1 cRNA induced dose-dependent sperm-like calcium oscillations whose frequency increased over time. Injection of bovine and mouse PLCZ1 cRNA also induced IP~3~R-1 degradation, although bovine PLCZ1 cRNA evoked greater receptor degradation than its mouse counterpart.

Conclusion

Injection of PLCZ1 cRNA efficiently activated bovine oocytes by inducing a sperm-like calcium oscillatory pattern. Importantly, the high rate of aneuploidy encountered in parthenogenetic embryos activated by certain chemical means was not observed in PLCZ1 activated embryos.


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## Abstract The response to parthenogenetic activation (calcium ionophore A23187) of bovine oocytes after 30 hr of culture in different maturation conditions was evaluated. The activation rates of oocytes in response to 10 ΞΌ A23187 were similar (86% Β± 4 vs. 89% Β± 8) when the oocytes matured with or