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首页> 外文期刊>Cell Structure and Function >Expression of selected apoptosis related genes, MIF, IGIF and TNF alpha, during retinoic acid-induced neural differentiation in murine embryonic stem cells
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Expression of selected apoptosis related genes, MIF, IGIF and TNF alpha, during retinoic acid-induced neural differentiation in murine embryonic stem cells

机译:维甲酸诱导的小鼠胚胎干细胞神经分化过程中与凋亡相关基因MIF,IGIF和TNFα的表达

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摘要

Apoptosis plays an important role during embryonic development. Apoptotic cell death is executed by caspases and can be regulated by the Bcl-2 family of genes. Ribonuclease protection assay was used to investigate the expression of selected apoptosis-related genes of the Bcl-2 family, pro-apoptotic Bax, Bad and antiapoptotic Bcl-2, during differentiation of murine embryonic stem cells (ES) mediated by all-trans-retinoic acid. The mRNA expression of caspase 3, caspase 6 and certain pro-inflammatory cytokines was also investigated simultaneously. ES cells exposed to 1 muM all-trans-retinoic acid on day 8, 9 and 10 of differentiation revealed increased expression of Bax and Bad compared to the vehicle-treated cells. No effect on Bcl-2 mRNA was noted after all-trans-retinoic acid treatment. Increased mRNA expression of caspase 3 and caspase 6 in all-trans-retinoic acid-exposed ES cells suggested that caspases play an important role in retinoic acid-mediated apoptosis during ES differentiation. Increase in the expression of TNFalpha and macrophage migration inhibitory factor (MIF) was noted in retinoic acid-treated cells on day 14. Significant increase observed in interferon gamma inducing factor (IGIF/IL-18) mRNA expression in all-trans-retinoic acid-treated cells on day 14 and 17 did not translate to increased INFgamma expression. No change in the expression of other pro-inflammatory cytokines was noted with all-trans-retinoic acid treatment. The function of TNFalpha, IGIF/IL-18 and MIF in all-trans-retinoic acid-treated cells during ES differentiation and apoptosis is still speculatory. Results suggested that RA-mediated apoptosis during neural differentiation of ES cells involves up-regulation of caspase 3, caspase 6, Bad, and Bax. [References: 48]
机译:细胞凋亡在胚胎发育中起重要作用。凋亡的细胞死亡是由胱天蛋白酶引起的,并且可以由Bcl-2基因家族调节。使用核糖核酸酶保护实验来研究在全反式介导的鼠胚胎干细胞(ES)分化过程中,Bcl-2家族,凋亡相关的Bax,Bad和抗凋亡Bcl-2所选凋亡相关基因的表达。视黄酸。同时研究了胱天蛋白酶3,胱天蛋白酶6和某些促炎细胞因子的mRNA表达。与分化处理的细胞相比,在分化的第8、9和10天暴露于1μM全反式维甲酸的ES细胞显示Bax和Bad的表达增加。全反式维甲酸处理后,未观察到对Bcl-2 mRNA的影响。在全反式维甲酸暴露的ES细胞中caspase 3和caspase 6的mRNA表达增加表明,胱天蛋白酶在ES分化过程中在维甲酸介导的细胞凋亡中起重要作用。在第14天,在视黄酸处理的细胞中发现TNFalpha和巨噬细胞迁移抑制因子(MIF)的表达增加。在全反式视黄酸中观察到干扰素γ诱导因子(IGIF / IL-18)mRNA表达的显着增加。在第14天和第17天处理的细胞未转化为增加的INFγ表达。全反式视黄酸处理未观察到其他促炎细胞因子表达的变化。 TNFα,IGIF / IL-18和MIF在全反式维甲酸处理的细胞分化和凋亡过程中的功能仍是推测性的。结果表明在ES细胞神经分化过程中RA介导的凋亡涉及caspase 3,caspase 6,Bad和Bax的上调。 [参考:48]

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