首页> 美国卫生研究院文献>PLoS Clinical Trials >Proliferation-Stimulating Effect of Colony Stimulating Factor 2 on Porcine Trophectoderm Cells Is Mediated by Activation of Phosphatidylinositol 3-Kinase and Extracellular Signal-Regulated Kinase 1/2 Mitogen-Activated Protein Kinase
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Proliferation-Stimulating Effect of Colony Stimulating Factor 2 on Porcine Trophectoderm Cells Is Mediated by Activation of Phosphatidylinositol 3-Kinase and Extracellular Signal-Regulated Kinase 1/2 Mitogen-Activated Protein Kinase

机译:磷脂酰肌醇3-激酶的激活和细胞外信号调节激酶1/2丝裂原活化的蛋白激酶介导集落刺激因子2对猪滋养外胚层细胞的增殖刺激作用。

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摘要

Colony-stimulating factor 2 (CSF2), also known as granulocyte macrophage colony-stimulating factor, facilitates mammalian embryonic development and implantation. However, biological functions and regulatory mechanisms of action of porcine endometrial CSF2 in peri-implantation events have not been elucidated. The aim of present study was to determine changes in cellular activities induced by CSFs and to access CSF2-induced intracellular signaling in porcine primary trophectoderm (pTr) cells. Differences in expression of CSF2 mRNA in endometrium from cyclic and pregnant gilts were evaluated. Endometrial CSF2 mRNA expression increases during the peri-implantation period, Days 10 to 14 of pregnancy, as compared to the estrous cycle. pTr cells obtained in Day 12 of pregnancy were cultured in the presence or absence of CSF2 (20 ng/ml) and (20 µM), U0126 (20 µM), rapamycin (20 nM), and SB203580 (20 µM). CSF2 in pTr cell culture medium at 20 ng/ml significantly induced phosphorylation of AKT1, ERK1/2, MTOR, p70RSK and RPS6 protein, but not STAT3 protein. Also, the PI3K specific inhibitor () abolished CSF2-induced increases in p-ERK1/2 and p-MTOR proteins, as well as CSF2-induced phosphorylation of AKT1. Changes in proliferation and migration of pTr cells in response to CSF2 were examined in dose- and time-response experiments. CSF2 significantly stimulated pTr cell proliferation and, U0126, rapamycin and blocked this CSF2-induced proliferation of pTr cells. Collectively, during the peri-implantation phase of pregnancy in pigs, endometrial CSF2 stimulates proliferation of trophectoderm cells by activation of the PI3K-and ERK1/2 MAPK-dependent MTOR signal transduction cascades.
机译:集落刺激因子2(CSF2),也称为粒细胞巨噬细胞集落刺激因子,可促进哺乳动物胚胎的发育和植入。然而,尚未阐明猪子宫内膜CSF2在植入前后的生物学功能和作用的调控机制。本研究的目的是确定猪原发性滋养外胚层(pTr)细胞中CSFs诱导的细胞活性的变化并获得CSF2诱导的细胞内信号传导。评价了周期性和后备母猪子宫内膜中CSF2 mRNA表达的差异。与动情周期相比,子宫内膜中CSF2 mRNA表达在植入后的怀孕10至14天期间增加。在有或没有CSF2(20 ng / ml)和(20 µM),U0126(20 µM),雷帕霉素(20 nM)和SB203580(20 µM)的情况下培养在妊娠第12天获得的pTr细胞。 pTr细胞培养基中的CSF2浓度为20 ng / ml时,可显着诱导AKT1,ERK1 / 2,MTOR,p70RSK和RPS6蛋白磷酸化,而不会引起STAT3蛋白磷酸化。此外,PI3K特异性抑制剂()消除了CSF2诱导的p-ERK1 / 2和p-MTOR蛋白的增加,以及CSF2诱导的AKT1磷酸化。在剂量和时间响应实验中检查了响应于CSF2的pTr细胞增殖和迁移的变化。 CSF2显着刺激pTr细胞增殖,U0126刺激雷帕霉素并阻断CSF2诱导的pTr细胞增殖。总的来说,在猪怀孕的围着床植入阶段,子宫内膜CSF2通过激活PI3K和ERK1 / 2 MAPK依赖性MTOR信号转导级联反应刺激滋养外胚层细胞的增殖。

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