Homa S T
Department of Zoology, Arizona State University, Tempe 85287.
J Exp Zool. 1991 Apr;258(1):95-103. doi: 10.1002/jez.1402580111.
The possibility that the intracellular signals generated upon phosphoinositide hydrolysis are involved in regulating bovine oocyte spontaneous meiotic resumption was investigated. Oocytes were mass-harvested and cultured in 2A-BMOC medium supplemented with 0.5% bovine serum albumin in the presence or absence of neomycin (an inhibitor of phosphoinositide hydrolysis) or phorbol myristate acetate (an activator of protein kinase C). The role of intracellular calcium was examined by preloading with BAPTA/AM (a calcium chelator) prior to culture. Meiotic maturation was scored cytogenetically. 1) Neomycin induces an irreversible inhibition of germinal vesicle breakdown which does not exceed 60% and is apparent at concentrations of 5 mM or above. Progression of meiosis past metaphase I is inhibited at concentrations of 2.5 mM or above. The full effect of neomycin is only apparent if it is presented to the oocytes within 3 h of follicular release, although germinal vesicle breakdown is not observed until 9 h culture under control conditions. 2) PMA alone has negligible effect on germinal vesicle breakdown, but it acts synergistically with 2 mM IBMX to inhibit this process. PMA has a dual effect on the progression of meiosis past metaphase I: 1 nM PMA has a stimulatory effect while 1 microM PMA blocks the ability of oocytes to reach anaphase I or beyond. These observations are not found with a non-tumor-promoting phorbol ester. 3) Spontaneous meiotic resumption is not significantly affected in the absence of added exogenous calcium. However, oocytes preloaded with BAPTA/AM exhibit a dose-dependent inhibition of germinal vesicle breakdown, even in the presence of extracellular calcium.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了磷酸肌醇水解产生的细胞内信号参与调节牛卵母细胞自发减数分裂恢复的可能性。大量采集卵母细胞,在添加0.5%牛血清白蛋白的2A - BMOC培养基中培养,分别添加新霉素(磷酸肌醇水解抑制剂)或佛波酯(蛋白激酶C激活剂),或二者都不添加。在培养前用BAPTA/AM(一种钙螯合剂)预加载来检测细胞内钙的作用。通过细胞遗传学方法对减数分裂成熟进行评分。1)新霉素对生发泡破裂诱导不可逆抑制,抑制率不超过60%,在5 mM及以上浓度时明显。在2.5 mM及以上浓度时,减数分裂向中期I后的进程受到抑制。新霉素的全部作用只有在卵泡释放后3小时内作用于卵母细胞时才明显,尽管在对照条件下培养9小时才观察到生发泡破裂。2)单独的佛波酯对生发泡破裂影响可忽略不计,但它与2 mM异丁基甲基黄嘌呤协同作用抑制此过程。佛波酯对减数分裂向中期I后的进程有双重作用:1 nM佛波酯有刺激作用,而1 microM佛波酯阻断卵母细胞到达后期I或更后期的能力。非促肿瘤佛波酯未观察到这些现象。3)在不添加外源钙的情况下,自发减数分裂恢复未受到显著影响。然而,即使存在细胞外钙,用BAPTA/AM预加载的卵母细胞也表现出生发泡破裂的剂量依赖性抑制。(摘要截断于250字)