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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Role of calcium-sensing receptor in regulating spontaneous activation of postovulatory aging rat oocytes
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Role of calcium-sensing receptor in regulating spontaneous activation of postovulatory aging rat oocytes

机译:钙传感受体在调节后衰老大鼠卵母细胞的自发激活中的作用

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摘要

Mechanisms for postovulatory aging (POA) of oocytes and for spontaneous activation (SA) of rat oocytes are largely unknown. Expression of calcium-sensing receptor (CaSR) in rat oocytes and its role in POA remain unexplored. In this study, expression of CaSR in rat oocytes aging for different times was detected by immunofluorescence microscopy, and western blotting and the role of CaSR in POA was determined by observing the effects of regulating its activity on SA susceptibility and cytoplasmic calcium levels. The results showed that CaSR was expressed in rat oocytes. Oocytes recovered 19 h post human chorionic gonadotropin (hCG) injection were more susceptible to SA and expressed more functional CaSR than oocytes recovered 13 h after hCG injection, although both expressed the same level of total CaSR protein. Treatment with CaSR antagonist significantly suppressed cytoplasmic calcium elevation and SA of oocytes. Activation ofNa-Ca2+ exchanger with NaCl inhibited SA to a greater extent than suppression of CaSR with NPS-2143, suggesting that calcium sources other than CaSR-controlled channels contributed to the elevation of cytoplasmic calcium. Treatment with T-or L-type calcium channel blockers significantly reduced SA. Suppression of all calcium channels tested reduced SA to minimum. It is concluded that the level of CaSR functional dimer protein, but not that of the total CaSR protein, was positively correlated with the SA susceptibility during POA of rat oocytes confirming that CaSR is involved in POA regulation. Blocking multiple calcium channels might be a better choice for efficient control of SA in rat oocytes.
机译:卵母细胞的后衰老(POA)和大鼠卵母细胞的自发激活(SA)的机制在很大程度上是未知的。钙传感受体(CASR)在大鼠卵母细胞中的表达及其在POA中的作用仍未开发。在该研究中,通过免疫荧光显微镜检测对不同时间的大鼠卵母细胞造成的CasR的表达,并通过观察调节其活性对SA易感性和细胞质钙水平的影响来确定POA中的蛋白质印迹和Casr的作用。结果表明,Casr在大鼠卵母细胞中表达。卵母细胞恢复19小时后,人绒毛膜促性腺激素(HCG)注射液更易于SA,并且表达了比HCG注射后13小时回收13小时的卵母细胞的更官能肠道,尽管两者都表达了相同的总Casr蛋白水平。 Casr拮抗剂治疗显着抑制了卵母细胞的细胞质钙升高和SA。与NaCl的抑制Sa的抑制Sa的抑制作用,而不是用NPS-2143的抑制抑制Sa,这表明除了Casr控制通道之外的钙源有助于细胞质钙的升高。用T-或L型钙通道的处理显着减少SA。所有钙通道的抑制测试还原到最小。结论是,Casr功能二聚体蛋白的水平,但不是总Casr蛋白的水平与大鼠卵母细胞Poa的SA易感性正相关,确认Casr参与PoA调节。阻断多个钙通道可能是在大鼠卵母细胞中有效控制SA的更好选择。

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