Several signaling pathways are involved in the control of cattle oocyte maturation

促成熟因子 生物 细胞生物学 磷酸化 卵母细胞 蛋白激酶B 激酶 卵母细胞激活 生物化学 细胞周期蛋白依赖激酶1 胚胎 细胞周期 细胞凋亡
作者
C. Vigneron,C. Perreau,Joëlle Dupont,Svetlana Uzbekova,Claude Prigent,Pascal Mermillod
出处
期刊:Molecular Reproduction and Development [Wiley]
卷期号:69 (4): 466-474 被引量:51
标识
DOI:10.1002/mrd.20173
摘要

Abstract The main limit of in vitro production of domestic mammal embryos comes from the low capacity of in vitro matured oocytes to develop after fertilization. As soon as they are separated from follicular environment, oocytes spontaneously resume meiosis without completion of their terminal differentiation. Roscovitine (ROS), an inhibitor of M‐phase promoting factor (MPF) kinase activity reversibly blocks the meiotic resumption in vitro. However, in cattle maturing oocytes several cellular events such as protein synthesis and phosphorylation, chromatin condensation and nuclear envelope folding escape ROS inhibition suggesting the alternative pathways in oocyte maturation. We compared the level of synthesis and phosphorylation of several protein kinases during bovine cumulus oocyte complex (COC) maturation in vitro in the presence or not of epidermal growth factor (EGF) and ROS. We showed that during the EGF‐stimulated maturation, ROS neither affected the decrease of EGF receptor (EGFR) nor did inhibit totally its phosphorylation in cumulus cells and also did not totally eliminate tyrosine phosphorylation in oocytes. However, ROS did inhibit the Phosphoinositide 3‐kinase (PI3) activity when oocytes mature without EGF. Accumulation of Akt/PKB (protein kinase B), JNK1/2 (jun N‐terminal kinases) and Aurora‐A in oocytes during maturation was not affected by ROS. However, the phosphorylation of Akt but not JNKs was diminished in ROS‐treated oocytes. Thus, PI3 kinase/Akt, JNK1/2 and Aurora‐A are likely to be involved in the regulation of bovine oocyte maturation and some of these pathways seem to be independent to MPF activity and meiotic resumption. This complex regulation may explain the partial meiotic arrest of ROS‐treated oocytes and the accelerated maturation observed after such treatment. Mol. Reprod. Dev. 69: 466–474, 2004. © 2004 Wiley‐Liss, Inc.
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