Wu Changli, Li Rong, Luo Haibing, Xu Mingfeng, Zhang Xiujuan
Department of Physiology, Guangdong Medical University, Zhanjiang, Guangdong, People's Republic of China.
Department of Pathophysiology, Guangdong Medical University, Zhanjiang, Guangdong, People's Republic of China.
Biosci Rep. 2017 Jul 12;37(4). doi: 10.1042/BSR20170642. Print 2017 Aug 31.
The inhibitor CEP-33779 is a specific selective inhibitor of Janus kinase 2 (JAK2). In most somatic cells, JAK2 plays essential roles in cellular signal transduction and in the regulation of cell cycle. Little is known regarding the effects of JAK2 on mammalian oocyte maturation. In the present study, we investigated the effects of CEP-33779 on mouse oocytes' meiosis and the possible mechanisms of JAK2 during mouse oocyte maturation. We detected the distribution of JAK2 during the mouse oocyte maturation. The results showed that JAK2 was mainly distributed in the cytoplasm during maturation. We cultured mouse oocytes with CEP-33779, examined the maturation rate, spindle morphology, and organization of microfilaments during the mouse oocyte maturation. While the rate of germinal vesicle breakdown (GVBD) did not differ between the treated and control groups, the rate of oocyte maturation decreased significantly when treated with CEP-33779. The rate of maturation was 21.14% in treated group and was 81.44% in control group. The results show that CEP-33779 inhibits the maturation of mouse oocytes. There was no obvious difference in the meiotic spindle morphology between the treated and control groups. The results show that CEP-33779 treatment did not disrupt the reorganization of microtubules. The microfilament observation shows that the microfilament did not form actin cap and the spindle stayed at the center of the oocyte in the treated group. CEP-33779 treatment inhibited the maturation of mouse oocytes which might be because of the disruption of formation of the actin cap. These results suggest that JAK2 regulated the microfilaments aggregation during the mouse oocyte maturation.
抑制剂CEP - 33779是一种特异性的Janus激酶2(JAK2)选择性抑制剂。在大多数体细胞中,JAK2在细胞信号转导和细胞周期调控中发挥着重要作用。关于JAK2对哺乳动物卵母细胞成熟的影响知之甚少。在本研究中,我们研究了CEP - 33779对小鼠卵母细胞减数分裂的影响以及JAK2在小鼠卵母细胞成熟过程中的可能机制。我们检测了JAK2在小鼠卵母细胞成熟过程中的分布。结果表明,JAK2在成熟过程中主要分布在细胞质中。我们用CEP - 33779培养小鼠卵母细胞,检测小鼠卵母细胞成熟过程中的成熟率、纺锤体形态和微丝组织。虽然处理组和对照组之间生发泡破裂(GVBD)率没有差异,但用CEP - 33779处理时卵母细胞成熟率显著降低。处理组的成熟率为21.14%,对照组为81.44%。结果表明,CEP - 33779抑制小鼠卵母细胞的成熟。处理组和对照组之间减数分裂纺锤体形态没有明显差异。结果表明,CEP - 33779处理不会破坏微管的重组。微丝观察显示,处理组微丝未形成肌动蛋白帽,纺锤体停留在卵母细胞中心。CEP - 33779处理抑制小鼠卵母细胞的成熟,这可能是由于肌动蛋白帽形成的破坏。这些结果表明,JAK2在小鼠卵母细胞成熟过程中调节微丝聚集。