生发泡
卵母细胞
米贝夫拉地尔
细胞生物学
卵母细胞激活
塔普斯加尔金
体外成熟
钙
化学
钌红
线粒体
生物
电压依赖性钙通道
细胞内
胚胎
有机化学
作者
Feng Wang,Li‐Hua Fan,Ang Li,Feng Dong,Yi Hou,Heide Schatten,Qing‐Yuan Sun,Xiang‐Hong Ou
摘要
Abstract Ca 2+ participates in many important cellular processes, but the underlying mechanisms are still poorly understood, especially during oocyte maturation. First, we confirmed that calcium in the culture medium was essential for oocyte maturation. Next, various inhibitors of Ca 2+ channels were applied to investigate their roles in mitochondrial Ca 2+ changes and oocyte maturation. Our results showed that Trmp7, Orai, T‐type Ca 2+ channels and Na + /Ca 2+ exchanger complex (NCLX) were important for oocyte maturation. Trmp7 inhibition delayed germinal vesicle breakdown. Orai and NCLX inhibition significantly weakened the distribution of mitochondrial Ca 2+ around the nucleus compared to the Ctrl group. Interestingly, even T‐type Ca 2+ channels‐specific inhibitor Mibefradil blocked germinal vesicle breakdown; mitochondrial Ca 2+ surrounding the nucleus still was maintained at a high level without spindle formation. Two calcium transporter inhibitors, Thapsigargin and Ruthenium Red, which have been confirmed to inhibit oocyte activation, did not significantly affect oocyte maturation. Increasing the knowledge of calcium transport may provide a basis to build on for improving oocyte in vitro maturation in human assisted reproduction clinics.
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