首页> 外文期刊>The Journal of Reproduction and Development >Extracellular glucose levels in cultures of undifferentiated mouse trophoblast stem cells affect gene expression during subsequent differentiation with replicable cell line-dependent variation
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Extracellular glucose levels in cultures of undifferentiated mouse trophoblast stem cells affect gene expression during subsequent differentiation with replicable cell line-dependent variation

机译:未分化的小鼠滋养细胞干细胞培养物中的细胞外血糖水平影响随后的分化过程中的基因表达,与可复制的细胞系依赖性变化

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摘要

Mouse trophoblast stem cells (TSCs) have been established and maintained using hyperglycemic conditions (11 mM glucose) for no apparent good reason. Because glucose metabolites are used as resources for cellular energy production, biosynthesis, and epigenetic modifications, differences in extracellular glucose levels may widely affect cellular function. Since the hyperglycemic culture conditions used for TSC culture have not been fully validated, the effect of extracellular glucose levels on the properties of TSCs remains unclear. To address this issue, we investigated the gene expression of sternness-related transcription factors in TSCs cultured in the undifferentiated state under various glucose concentrations. We also examined the expression of trophoblast subtype markers during differentiation, after returning the glucose concentration to the conventional culture concentration (11 mM). As a result, it appeared that the extracellular glucose conditions in the stem state not only affected the gene expression of stemness-related transcription factors before differentiation but also affected the expression of marker genes after differentiation, with some line-to-line variation. In the TS4 cell line, which showed the largest glucose concentration-dependent fluctuations in gene expression among all the lines examined, low glucose (1 mM glucose, LG) augmented H3K27me3 levels. An Ezh2 inhibitor prevented these LG-induced changes in gene expression, suggesting the possible involvement of H3K27me3 in the changes in gene expression seen in LG. These results collectively indicate that the response of the TSCs to the change in the extracellular glucose concentration is cell line-dependent and a part of which may be epigenetically memorized.
机译:小鼠滋养细胞干细胞(TSCs)已经建立并维持使用高血糖条件(11mm葡萄糖),无明显好理由。因为葡萄糖代谢物被用作细胞能量生产的资源,生物合成和表观遗传修饰,细胞外葡萄糖水平的差异可能广泛影响细胞功能。由于用于TSC培养的高血糖培养条件尚未完全验证,因此细胞外血糖水平对TSC的性质的影响尚不清楚。为了解决这一问题,我们研究了在各种葡萄糖浓度下在未分化状态下培养的TSCs中似乎相关转录因子的基因表达。在将葡萄糖浓度归入到常规培养浓度(11mm)之后,我们还检查了分化过程中滋养细胞亚型标记物的表达。结果,似乎茎状态的细胞外葡萄糖条件不仅影响了分化前茎与茎相关转录因子的基因表达,而且影响了分化后标记基因的表达,具有一些线到线变异。在TS4细胞系中,在检查的所有线中显示出基因表达中最大的葡萄糖浓度依赖性波动,低葡萄糖(1mM葡萄糖,LG)增强H3K27ME3水平。 EZH2抑制剂防止了这些LG诱导的基因表达的变化,表明H3K27ME3可能涉及H3K27ME3在LG中所见的基因表达的变化中。这些结果集体表明TSCs对细胞外葡萄糖浓度的变化的响应是细胞系依赖性,并且其一部分可以表现出外观记忆。

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