首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Effects of leptin and leukemia inhibitory factor on preimplantation development and STAT3 signaling of mouse embryos in vitro
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Effects of leptin and leukemia inhibitory factor on preimplantation development and STAT3 signaling of mouse embryos in vitro

机译:瘦素和白血病抑制因子对小鼠胚胎着床前发育和STAT3信号的影响

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Preimplantation mouse embryos simultaneously express receptors for leptin and leukemia inhibitory factor (LIF), both of which trigger activation of STAT3 (Signal Transducer and Activator of Transcription) protein. To examine the joint effects of leptin and LIF on embryonic development, we studied preimplantation development and activation of STAT3 signaling of mouse embryos after exposure to leptin and/or LIF in vitro. Two-cell mouse embryos (Day 2) were cultured in the presence of leptin and/or LIF. Significantly fewer leptin-exposed than control embryos hatched by Day 5 and by Day 6 of development. In addition, cells of leptin-exposed Day 5 blastocysts showed a higher rate of DNA fragmentation, which is a sign of apoptosis. Leukemia inhibitory factor alone had no effect on the rates of embryonic development or DNA fragmentation. Simultaneous exposure of embryos to leptin and LIF increased the proportion of hatching embryos and decreased the rate of apoptosis compared to embryos exposed to leptin only. Leptin treatment was associated with an increased phospho-STAT3-specific immunofluorescence in the cell membrane of blastocysts, which was not observed in LIF-exposed embryos. In conclusion, LIF modifies the effect of leptin during preimplantation embryo development in mice, presumably by interfering with activation of STAT3 signaling. [References: 45]
机译:植入前的小鼠胚胎同时表达瘦素和白血病抑制因子(LIF)的受体,二者均可触发STAT3(信号转导和转录激活剂)蛋白的激活。为了检查瘦素和LIF对胚胎发育的联合作用,我们研究了在体外暴露于瘦素和/或LIF后小鼠胚胎着床前的发育和STAT3信号的激活。在瘦蛋白和/或LIF存在下培养两细胞小鼠胚胎(第2天)。与发育第5天和第6天孵化的对照胚胎相比,瘦素暴露量显着减少。此外,暴露于瘦素的第5天胚泡细胞显示出更高的DNA断裂率,这是细胞凋亡的迹象。单独的白血病抑制因子对胚胎发育或DNA断裂的速率没有影响。与仅暴露于瘦蛋白的胚胎相比,将胚胎同时暴露于瘦蛋白和LIF会增加孵化胚胎的比例,并降低凋亡率。瘦素治疗与胚泡细胞膜中磷酸化STAT3特异性免疫荧光增强有关,而在LIF暴露的胚胎中未观察到。总之,LIF可能通过干扰STAT3信号的激活来调节小鼠植入前胚胎发育过程中瘦蛋白的作用。 [参考:45]

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