Hirohashi Noritaka, Harada Kaori, Chiba Kazuyoshi
Genetic Counseling Program, Graduate School of Humanities and Sciences, Ochanomizu University, 2-1-1 Otsuka, Bunkyo, Tokyo 112-8610, Japan.
Dev Biol. 2008 Jun 1;318(1):194-202. doi: 10.1016/j.ydbio.2008.03.029. Epub 2008 Mar 28.
Meiotic progression in starfish oocytes is reinitiated by a maturation-inducing hormone called 1-methyladenine (1-MeAde). In addition to meiotic maturation, 1-MeAde induces cortical maturation in which cortical granules become competent to discharge in response to fusion of a single sperm, which results in the formation of the fertilization envelope. We found that subthreshold concentrations of 1-MeAde induce cortical maturation without germinal vesicle breakdown (GVBD). During cortical maturation, the IP3 sensitivity of calcium stores was increased as well as during meiotic maturation. When oocytes were exposed with 1-MeAde only on a hemisphere of oocytes, the IP3 sensitivity of the cortical region was increased only in the exposed hemisphere, suggesting that signals and components involved in cortical maturation do not readily spread in the cytoplasm. Although a specific inhibitor of phosphatidylinositol-3 kinase, LY294002 blocked both GVBD and cortical maturation, a Cdc2 kinase inhibitor, roscovitine did not block cortical maturation. Inhibition of Akt activation by injecting the competitors for Akt phosphorylation and membrane recruitment also blocked cortical maturation. These results suggest that the signaling pathway leading to Akt activation is common in cortical maturation and meiotic maturation, and Cdc2 activation was not required for cortical maturation.
海星卵母细胞的减数分裂进程由一种名为1-甲基腺嘌呤(1-MeAde)的成熟诱导激素重新启动。除了减数分裂成熟外,1-MeAde还诱导皮质成熟,其中皮质颗粒在单个精子融合时能够释放,从而导致受精膜的形成。我们发现,亚阈值浓度的1-MeAde可诱导皮质成熟而不发生生发泡破裂(GVBD)。在皮质成熟过程中,钙库的IP3敏感性增加,减数分裂成熟过程中也是如此。当卵母细胞仅在卵母细胞的一个半球暴露于1-MeAde时,皮质区域的IP3敏感性仅在暴露的半球增加,这表明参与皮质成熟的信号和成分不容易在细胞质中扩散。虽然磷脂酰肌醇-3激酶的特异性抑制剂LY294002可阻断GVBD和皮质成熟,但Cdc2激酶抑制剂roscovitine并不阻断皮质成熟。通过注射Akt磷酸化和膜募集的竞争剂抑制Akt激活也可阻断皮质成熟。这些结果表明,导致Akt激活的信号通路在皮质成熟和减数分裂成熟中是常见的,并且皮质成熟不需要Cdc2激活。