首页> 外文期刊>Reproduction, fertility, and development >Oncostatin M and leukaemia inhibitory factor trigger signal transducer and activator of transcription 3 and extracellular signal-regulated kinase 1/2 pathways but result in heterogeneous cellular responses in trophoblast cells
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Oncostatin M and leukaemia inhibitory factor trigger signal transducer and activator of transcription 3 and extracellular signal-regulated kinase 1/2 pathways but result in heterogeneous cellular responses in trophoblast cells

机译:抑瘤素M和白血病抑制因子触发信号转导和转录激活因子3以及细胞外信号调节激酶1/2途径,但导致滋养层细胞发生异质性细胞应答

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摘要

Leukaemia inhibitory factor (LIF) and oncostatin M (OSM) are pleiotropic cytokines present at the implantation site that are important for the normal development of human pregnancy. These cytokines share the cell membrane receptor subunit gp130, resulting in similar functions. The aim of this study was to compare the response to LIF and OSM in several trophoblast models with particular regard to intracellular mechanisms and invasion. Four trophoblast cell lines with different characteristics were used: HTR-8/SVneo, JEG-3, ACH-3P and AC1-M59 cells. Cells were incubated with LIF, OSM (both at 10ngmL(-1)) and the signal transducer and activator of transcription (STAT) 3 inhibitor S3I-201 (200 mu M). Expression and phosphorylation of STAT3 (tyr(705)) and extracellular regulated kinase (ERK) 1/2 (thr(202/204)) and the STAT3 DNA-binding capacity were analysed by Western blotting and DNA-binding assays, respectively. Cell viability and invasiveness were assessed by the methylthiazole tetrazolium salt (MTS) and Matrigel assays. Enzymatic activity of matrix metalloproteinase (MMP)-2 and MMP-9 was investigated by zymography. OSM and LIF triggered phosphorylation of STAT3 and ERK1/2, followed by a significant increase in STAT3 DNA-binding activity in all tested cell lines. Stimulation with LIF but not OSM significantly enhanced invasion of ACH-3P and JEG-3 cells, but not HTR-8/SVneo or AC1-M59 cells. Similarly, STAT3 inhibition significantly decreased the invasiveness of only ACH-3P and JEG-3 cells concomitant with decreases in secreted MMP-2 and MMP-9. OSM shares with LIF the capacity to activate ERK1/2 and STAT3 pathways in all cell lines tested, but their resulting effects are dependent on cell type. This suggests that LIF and OSM may partially substitute for each other in case of deficiencies or therapeutic interventions.
机译:白血病抑制因子(LIF)和抑瘤素M(OSM)是存在于植入位点的多效性细胞因子,对人类妊娠的正常发展很重要。这些细胞因子共享细胞膜受体亚基gp130,从而产生相似的功能。这项研究的目的是比较几种滋养细胞模型对LIF和OSM的反应,特别是关于细胞内机制和侵袭的研究。使用了四个具有不同特征的滋养细胞细胞系:HTR-8 / SVneo,JEG-3,ACH-3P和AC1-M59细胞。将细胞与LIF,OSM(均为10ngmL(-1))和信号转导和转录激活因子(STAT)3抑制剂S3I-201(200μM)一起孵育。 STAT3(tyr(705))和细胞外调节激酶(ERK)1/2(thr(202/204))的表达和磷酸化以及STAT3 DNA的结合能力分别通过蛋白质印迹法和DNA结合法进行了分析。通过甲基噻唑四唑盐(MTS)和基质胶测定法评估细胞活力和侵袭性。通过酶谱研究基质金属蛋白酶(MMP)-2和MMP-9的酶活性。 OSM和LIF触发STAT3和ERK1 / 2的磷酸化,随后在所有测试的细胞系中STAT3 DNA结合活性显着增加。用LIF刺激而不是OSM刺激显着增强了ACH-3P和JEG-3细胞的侵袭,但没有增强HTR-8 / SVneo或AC1-M59细胞的侵袭。同样,STAT3的抑制作用显着降低了仅ACH-3P和JEG-3细胞的侵袭性,同时分泌的MMP-2和MMP-9降低了。 OSM与LIF共同具有激活所有测试细胞系中ERK1 / 2和STAT3途径的能力,但它们产生的作用取决于细胞类型。这表明在缺乏或进行治疗干预时,LIF和OSM可能部分替代。

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