首页> 美国卫生研究院文献>The Journal of Reproduction and Development >The Effects of Calcitonin on the Development of and Ca2+ Levels in Heat-shocked Bovine PreimplantationEmbryos In Vitro
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The Effects of Calcitonin on the Development of and Ca2+ Levels in Heat-shocked Bovine PreimplantationEmbryos In Vitro

机译:降钙素对热休克牛植入前钙和钙离子水平的影响体外胚胎

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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 < 0.05). The relative intracellular Ca2+ 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)不会影响卵裂率。然而,与在整个38.5 C下培养的对照相比,它显着降低了5至8细胞和胚泡阶段的发育速度(P <0.05)。通过Fluo-8 AM(一种用于Ca 2+ <的荧光探针)评估,在1个细胞阶段(热休克开始后5小时)的相对细胞内Ca 2 + 水平。 / sup>,表明热激比对照水平显着降低了Ca 2 + 的水平。半定量逆转录PCR和蛋白质印迹分析揭示了CT受体在牛植入前胚胎中的表达。在培养基中添加CT(10 nM)可以改善热休克诱导的5至8细胞阶段后胚胎发育的损害。 CT培养的热激胚胎中的Ca 2 + 水平与对照胚胎相似,表明热激降低了受精胚胎中Ca 2 + 的水平。在体外,较低的Ca 2 + 水平与热激诱导的胚胎发育损伤有关。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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