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确定型红细胞生成中的发育转变:促红细胞生成素的表达受视黄酸受体和肝细胞核因子4的顺序调控。

A developmental transition in definitive erythropoiesis: erythropoietin expression is sequentially regulated by retinoic acid receptors and HNF4.

作者信息

Makita T, Hernandez-Hoyos G, Chen T H, Wu H, Rothenberg E V, Sucov H M

机构信息

Department of Biochemistry and Molecular Biology, Institute for Genetic Medicine, University of Southern California Keck School of Medicine, Los Angeles, California 90033, USA.

出版信息

Genes Dev. 2001 Apr 1;15(7):889-901. doi: 10.1101/gad.871601.

Abstract

The cytokine erythropoietin (Epo) promotes erythropoietic progenitor cell proliferation and is required for erythropoietic differentiation. We have found that the Epo gene is a direct transcriptional target gene of retinoic acid signaling during early erythropoiesis (prior to embryonic day E12.5) in the fetal liver. Mouse embryos lacking the retinoic acid receptor gene RXR alpha have a morphological and histological phenotype that is comparable with embryos in which the Epo gene itself has been mutated, and flow cytometric analysis indicates that RXR alpha-deficient embryos are deficient in erythroid differentiation. Epo mRNA levels are reduced substantially in the fetal livers of RXR alpha(-/-) embryos at E10.25 and E11.25, and genetic analysis shows that the RXR alpha and Epo genes are coupled in the same pathway. We furthermore show that the Epo gene is retinoic acid inducible in embryos, and that the Epo gene enhancer contains a DR2 sequence that represents a retinoic acid receptor-binding site and a retinoic acid receptor transcriptional response element. However, unlike Epo-deficient embryos that die from anemia, the erythropoietic deficiency in RXR alpha(-/-) embryos is transient; Epo mRNA is expressed at normal levels by E12.5, and erythropoiesis and liver morphology are normal by E14.5. We show that HNF4, like RXR alpha a member of the nuclear receptor family, is abundantly expressed in fetal liver hepatocytes, and is competitive with retinoic acid receptors for occupancy of the Epo gene enhancer DR2 element. We propose that Epo expression is regulated during the E9.5--E11.5 phase of fetal liver erythropoiesis by RXR alpha and retinoic acid, and that expression then becomes dominated by HNF4 activity from E11.5 onward. This transition may be responsible for switching regulation of Epo expression from retinoic acid control to hypoxic control, as is found throughout the remainder of life.

摘要

细胞因子促红细胞生成素(Epo)可促进促红细胞生成祖细胞增殖,是红细胞生成分化所必需的。我们发现,在胎儿肝脏早期红细胞生成过程中(胚胎第E12.5天之前),Epo基因是视黄酸信号的直接转录靶基因。缺乏视黄酸受体基因RXRα的小鼠胚胎具有与Epo基因本身发生突变的胚胎相当的形态学和组织学表型,流式细胞术分析表明,RXRα缺陷型胚胎在红细胞分化方面存在缺陷。在E10.25和E11.25时,RXRα(-/-)胚胎的胎儿肝脏中Epo mRNA水平大幅降低,遗传分析表明,RXRα和Epo基因在同一途径中相互关联。我们进一步表明,Epo基因在胚胎中可被视黄酸诱导,且Epo基因增强子包含一个DR2序列,该序列代表视黄酸受体结合位点和视黄酸受体转录反应元件。然而,与因贫血而死亡的Epo缺陷型胚胎不同,RXRα(-/-)胚胎中的红细胞生成缺陷是短暂的;到E12.5时,Epo mRNA以正常水平表达,到E14.5时,红细胞生成和肝脏形态恢复正常。我们表明,与RXRα一样属于核受体家族成员的HNF4在胎儿肝脏肝细胞中大量表达,并且与视黄酸受体竞争占据Epo基因增强子DR2元件。我们提出,在胎儿肝脏红细胞生成的E9.5 - E11.5阶段,Epo表达受RXRα和视黄酸调控,而从E11.5开始,其表达则由HNF4活性主导。这种转变可能负责将Epo表达的调控从视黄酸控制切换为缺氧控制,这在生命的其余阶段也有发现。

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