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5-氮杂胞苷诱导10T1/2细胞形成稳定的中胚层干细胞谱系:控制细胞分化的调控基因的证据

5-Azacytidine induction of stable mesodermal stem cell lineages from 10T1/2 cells: evidence for regulatory genes controlling determination.

作者信息

Konieczny S F, Emerson C P

出版信息

Cell. 1984 Oct;38(3):791-800. doi: 10.1016/0092-8674(84)90274-5.

Abstract

5-Azacytidine converts the mouse embryonic cell line C3H 10T1/2 into differentiated chondrocytes, adipocytes, and skeletal muscle. Clonal and 2D protein gel analyses demonstrate that 5-azacytidine converts 10T1/2 cells into three stably determined, but undifferentiated, stem cell lineages which can differentiate into myofibers, chondrocytes, and adipocytes. Conversion of 10T1/2 cells is accompanied by specific changes in protein synthetic patterns unique for each cell lineage. We propose that 5-azacytidine converts 10T1/2 cells by hypomethylation of "determination" regulatory loci which establish lineages of stem cells with a restricted potential to differentiate into muscle, cartilage, or fat cells. Our results suggest that these three lineages are specified by separate regulatory loci and that as few as 1-3 hypomethylation events per cell are sufficient to activate the hypothesized muscle regulatory locus. Conversion of 10T1/2 cells by 5-azacytidine provides a model for studying regulatory genes involved in cell lineage determination.

摘要

5-氮杂胞苷可将小鼠胚胎细胞系C3H 10T1/2转化为分化的软骨细胞、脂肪细胞和骨骼肌细胞。克隆和二维蛋白质凝胶分析表明,5-氮杂胞苷将10T1/2细胞转化为三种稳定确定但未分化的干细胞谱系,这些谱系可分化为肌纤维、软骨细胞和脂肪细胞。10T1/2细胞的转化伴随着每个细胞谱系特有的蛋白质合成模式的特定变化。我们提出,5-氮杂胞苷通过“决定”调控位点的低甲基化来转化10T1/2细胞,这些位点建立了具有有限分化为肌肉、软骨或脂肪细胞潜力的干细胞谱系。我们的结果表明,这三种谱系由单独的调控位点指定,并且每个细胞少至1-3次低甲基化事件就足以激活假设的肌肉调控位点。5-氮杂胞苷对10T1/2细胞的转化为研究参与细胞谱系决定的调控基因提供了一个模型。

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