首页> 外文期刊>Cell biology international. >Serum-free mouse embryo cells generate a self-sustaining feedback loop for an astrocyte marker protein and respond to cytokines and bisphenol A in accordance with the subtle difference in their differentiation state.
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Serum-free mouse embryo cells generate a self-sustaining feedback loop for an astrocyte marker protein and respond to cytokines and bisphenol A in accordance with the subtle difference in their differentiation state.

机译:无血清的小鼠胚胎细胞产生星形胶质细胞标记蛋白的自我维持反馈环,并根据其分化状态的细微差别对细胞因子和双酚A作出反应。

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Serum-free mouse embryo (SFME) cells, the astrocyte progenitor cells in the central nervous system, generated a self-sustaining feedback loop for glial fibrillary acidic protein (GFAP) expression after a period of cell passages. The period required was about 150days (30 passages). SFME and high-GFAP-expressing SFME (G-SFME) cells were exposed to 10ng/ml leukemia inhibitory factor (LIF) and 10ng/ml bone morphogenetic protein 2 (BMP2) to induce differentiation and their responses to cytokine signals were analyzed. Although differentiation was significantly induced in both cell types, SFME cells showed more obvious responses to the cytokine signals. Various concentrations of bisphenol A (BPA) (0.1pg/ml to 1mug/ml) were added to determine its effects on cell differentiation. A completely serum-free culture was developed for effective differentiation of G-SFME cells with LIF and BMP2, and GFAP expression was significantly increased in the presence of 1-100pg/ml BPA. These increases were attributed to excessive activation of signal transducer and activator of transcription 3 (STAT3) and mothers against decapentaplegic homolog 1 (Smad1) by the low-level BPA. The data obtained in the present study revealed that the sensitivity of the cells to LIF, BMP2 and BPA could change upon cell differentiation, suggesting that the cells may possibly respond differently to cytokines and endocrine disruptors depending on subtle differences in their differentiation state.
机译:无血清小鼠胚胎(SFME)细胞是中枢神经系统中的星形胶质细胞祖细胞,经过一段时间的细胞传代后,产生了神经胶质原纤维酸性蛋白(GFAP)表达的自持性反馈环。所需时间约为150天(30遍)。将SFME和高表达GFAP的SFME(G-SFME)细胞暴露于10ng / ml白血病抑制因子(LIF)和10ng / ml骨形态发生蛋白2(BMP2)诱导分化,并分析其对细胞因子信号的反应。尽管在两种细胞类型中均显着诱导分化,但SFME细胞对细胞因子信号显示出更明显的响应。加入各种浓度的双酚A(BPA)(0.1pg / ml至1mug / ml),以确定其对细胞分化的影响。开发了一种完全无血清的培养物,用于通过LIF和BMP2有效分化G-SFME细胞,并且在1-100pg / ml BPA的存在下GFAP表达显着增加。这些增加归因于低水平的BPA过度激活了信号转导子和转录激活子3(STAT3),以及母亲对抗去能力障碍同系物1(Smad1)。在本研究中获得的数据表明,细胞对LIF,BMP2和BPA的敏感性可能随细胞分化而改变,这表明细胞可能根据其分化状态的细微差异而对细胞因子和内分泌干扰物做出不同反应。

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