Stage-specific gene expression in erythroid progenitor cells (CFU-E)

Yuji Mishina, Yasuhisa Matsui, Masuo Obinata
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引用次数: 4

Abstract

In erythropoietic differentiation, mature red blood cells are generated from specific progenitor cells through the action of specific growth regulatory molecules. To know the mechanism of differentiation, it is important to examine the control of gene expression in these progenitor cells in combination with growth regulatory molecules. We have cloned two genes expressing at a maximal level in the CFU-E (colony forming unit-erythroid), one of the erythroid progenitor cells from novel murine erythroleukemia (MEL) cell line (TSA8) which can be induced to CFU-E in vitro. The expression of these genes is well correlated with the appearance of CFU-E during induction of TSA8 cells, and is higher in the CFU-E-cells enriched from mouse fetal livers than in the more differentiated erythroid cells. Combining these with our previous results, it is suggested that in the erythropoiesis the progenitor cells have distinct patterns of gene expression. This expression is replaced through each progenitor cell rather than by the continuous increase in the expression of a set of genes specific to the mature erythroid cell following the commitment process.

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红细胞祖细胞(CFU-E)分期特异性基因表达
在红细胞生成分化中,成熟红细胞是由特定祖细胞通过特定生长调节分子的作用生成的。为了了解分化的机制,研究这些祖细胞中基因表达的调控与生长调节分子的结合是很重要的。我们克隆了两个在CFU-E (colony forming unit-erythroid)中表达最高水平的基因,CFU-E是来自新型小鼠红细胞白血病(MEL)细胞系(TSA8)的红系祖细胞之一,可以在体外诱导CFU-E。在TSA8细胞诱导过程中,这些基因的表达与CFU-E的出现密切相关,并且在小鼠胎肝富集的CFU-E细胞中的表达高于分化程度更高的红系细胞。结合我们之前的结果,提示在红细胞生成过程中,祖细胞具有不同的基因表达模式。这种表达在每个祖细胞中被取代,而不是在承诺过程中成熟红细胞特异性的一组基因的表达持续增加。
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