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首页> 外文期刊>The Journal of Reproduction and Development >The Effects of Calcitonin on the Development of and Ca2+ Levels in Heat-shocked Bovine Preimplantation Embryos In Vitro
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The Effects of Calcitonin on the Development of and Ca2+ Levels in Heat-shocked Bovine Preimplantation Embryos In Vitro

机译:降钙素对体外热激牛植入前胚胎发育和Ca 2 + 水平的影响

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摘要

Intracellular calcium homeostasis is essential for proper cell function. We investigated the effects of heat shock on the development of and the intracellular Ca2+ levels in bovine preimplantation embryos in vitro and the effects of calcitonin (CT), a receptor-mediated Ca2+ regulator, on heat shock-induced events. Heat shock (40.5 C for 10 h between 20 and 30 h postinsemination) of in vitro -produced bovine embryos did not affect the cleavage rate; however, it significantly decreased the rates of development to the 5- to 8-cell and blastocyst stages as compared with those of the control cultured for the entire period at 38.5 C (P 2+ levels at the 1-cell stage (5 h after the start of heat shock), as assessed by Fluo-8 AM, a fluorescent probe for Ca2+, indicated that heat shock significantly lowered the Ca2+ level as compared with the control level. Semiquantitative reverse transcription PCR and western blot analyses revealed the expression of CT receptor in bovine preimplantation embryos. The addition of CT (10 nM) to the culture medium ameliorated the heat shock-induced impairment of embryonic development beyond the 5- to 8-cell stage. The Ca2+ level in the heat-shocked embryos cultured with CT was similar to that of the control embryos, suggesting that heat shock lowers the Ca2+ level in fertilized embryos in vitro and that a lower Ca2+ level is implicated in heat shock-induced impairment of embryonic development. Intracellular Ca2+-mobilizing agents, e.g., CT, may effectively circumvent the detrimental effects of heat shock on early embryonic development.
机译:细胞内钙稳态对正常细胞功能至关重要。我们研究了热休克对体外牛植入前胚胎发育及其细胞内Ca 2 + 水平的影响,以及受体介导的Ca 2+降钙素(CT)的影响。 调节器,用于热冲击引发的事件。体外产生的牛胚胎的热激(40.5 C,在受精后20至30 h之间持续10 h)不影响卵裂率。然而,与在整个过程中于38.5 C(1-细胞阶段的P 2 + 水平)培养的对照相比,它显着降低了从5到8细胞和胚泡阶段的发育速度。 Ca 2 + 荧光探针Fluo-8 AM评估(热激开始后5小时),表明热激显着降低了Ca 2 + 对照水平>半定量逆转录PCR和Western blot分析揭示了牛植入前胚胎中CT受体的表达,向培养基中添加CT(10 nM)改善了热激诱导的胚胎发育障碍超过5到8个细胞阶段,CT培养的热激胚胎中的Ca 2 + 水平与对照胚胎相似,表明热激降低了Ca 体外受精胚胎中的2 + 水平和热休克中Ca 2 + 水平较低k诱导的胚胎发育受损。细胞内Ca 2 + 动员剂,例如CT,可以有效地规避热休克对早期胚胎发育的有害影响。

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