Gery Sigal, Park Dorothy J, Vuong Peter T, Chih Doris Y, Lemp Nathan, Koeffler H Phillip
Division of Hematology/Oncology, Cedars-Sinai Medical Center, University of California at Los Angeles, CA 90048, USA.
Blood. 2004 Dec 15;104(13):3911-7. doi: 10.1182/blood-2003-10-3688. Epub 2004 Aug 12.
Retinoic acid (RA) promotes granulocytic differentiation of normal hematopoietic cells and acute promyelocytic leukemia (APL) blasts by transcriptional modulation of myeloid regulatory genes. In this study, we have identified the C/EBP homologous protein (CHOP) as a novel retinoid-responsive gene using a polymerase chain reaction (PCR)-based cDNA subtraction method. All-trans retinoic acid (ATRA) induced a biphasic expression of CHOP mRNA in the NB4 and HL60 AML cell lines. Levels of CHOP expression increased within 1 hour of exposure to ATRA. ATRA expression became nearly absent between 6 and 24 hours, and a second phase of induction occurred after 48 hours. Retinoid-dependent regulation of CHOP expression was also observed in normal human neutrophils but not in peripheral blood mononuclear cells. In addition, retinoid-dependent regulation of CHOP expression was not observed in retinoid-nonresponsive cell lines HL60R and NB4-R2. CHOP expression was regulated at the transcriptional level and was independent of new protein synthesis. CHOP heterodimerized with C/EBPepsilon and negatively regulated the myeloid-specific gene lactoferrin. Furthermore, CHOP transcriptionally inhibited C/EBPalpha- and C/EBPepsilon-dependent induction of secondary granule gene expression. RA signaling in granulocytic differentiation involves regulated expression of CHOP and C/EBPepsilon in a coordinated fashion.
维甲酸(RA)通过对髓系调节基因的转录调控,促进正常造血细胞和急性早幼粒细胞白血病(APL)原始细胞的粒细胞分化。在本研究中,我们使用基于聚合酶链反应(PCR)的cDNA消减方法,鉴定出C/EBP同源蛋白(CHOP)是一种新的类维生素A反应基因。全反式维甲酸(ATRA)在NB4和HL60急性髓系白血病细胞系中诱导CHOP mRNA呈双相表达。CHOP表达水平在暴露于ATRA后1小时内升高。在6至24小时之间,ATRA表达几乎消失,48小时后出现第二阶段诱导。在正常人中性粒细胞中也观察到类维生素A依赖性的CHOP表达调节,但在外周血单个核细胞中未观察到。此外,在对类维生素A无反应的细胞系HL60R和NB4-R2中未观察到类维生素A依赖性的CHOP表达调节。CHOP表达在转录水平受到调控,且不依赖于新的蛋白质合成。CHOP与C/EBPε形成异二聚体,并对髓系特异性基因乳铁蛋白起负调控作用。此外,CHOP在转录水平上抑制C/EBPα和C/EBPε依赖性的次级颗粒基因表达诱导。粒细胞分化中的RA信号传导涉及CHOP和C/EBPε的协调调控表达。