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鉴定红细胞生成素诱导的造血细胞在红细胞分化过程中的 microRNAs。

Identification of erythropoietin-induced microRNAs in haematopoietic cells during erythroid differentiation.

机构信息

Integrative Bioscience and Biomedical Engineering, Graduate School of Science and Engineering, Waseda University, Tokyo, Japan.

出版信息

Br J Haematol. 2008 Jun;142(2):293-300. doi: 10.1111/j.1365-2141.2008.07151.x. Epub 2008 May 19.

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression through mRNA degradation or translation inhibition. It has not yet been clearly elucidated whether miRNAs participate in haematopoietic processes such as cell differentiation, apoptosis and maintenance of adequate levels of circulating blood cells. A human miRNA microarray was used to analyze miRNA expression in the erythropoietin-dependent cell line UT-7/EPO compared to other factor-dependent UT-7 cell lines. Among 324 human miRNAs, MIRN188, MIRN362 and MIRN210 levels were significantly elevated in UT-7/EPO cells, and stimulation with EPO in UT-7 cells increased the level of these three miRNAs. Notably, knockdown of MIRN210 in UT-7/EPO cells led to apoptosis. In mouse fetal liver cells, MIRN210 expression was twofold higher in TER-119-positive cells than in TER-119-negative cells. The expression of MIRN210 was elevated during erythroid maturation in vitro. These data suggest MIRN210 to be a member a new class of regulatory miRNAs that might play an important role in erythroid maturation.

摘要

MicroRNAs (miRNAs) 是一类小型非编码 RNA,通过 mRNA 降解或翻译抑制来调节基因表达。miRNAs 是否参与造血过程,如细胞分化、凋亡和维持循环血细胞的适当水平,目前尚不清楚。本研究采用人类 miRNA 微阵列,分析与其他因子依赖性 UT-7 细胞系相比,依赖促红细胞生成素的细胞系 UT-7/EPO 中的 miRNA 表达。在 324 个人类 miRNA 中,MIRN188、MIRN362 和 MIRN210 在 UT-7/EPO 细胞中的水平显著升高,EPO 刺激 UT-7 细胞也增加了这三种 miRNA 的水平。值得注意的是,在 UT-7/EPO 细胞中敲低 MIRN210 会导致细胞凋亡。在小鼠胎肝细胞中,TER-119 阳性细胞中的 MIRN210 表达是 TER-119 阴性细胞的两倍。体外红系成熟过程中 MIRN210 的表达升高。这些数据表明 MIRN210 是一类新的调节性 miRNA,可能在红系成熟中发挥重要作用。

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