Wei L N, Blaner W S, Goodman D S, Nguyen-Huu M C
Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York 10032.
Mol Endocrinol. 1989 Mar;3(3):454-63. doi: 10.1210/mend-3-3-454.
P19 embryonal carcinoma (EC) cells can be induced to differentiate in vitro into a variety of cell types by treatment with different concentrations of retinoic acid (RA). A study was conducted to explore the regulation of expression of the genes for cellular retinoic acid-binding protein (CRABP) and cellular retinol-binding protein (CRBP) in P19 cells induced to differentiate by RA. For each retinoid-binding protein, both the level of specific mRNA and of immunoreactive protein were measured, respectively, by RNase protection assay and by a specific RIA. Dramatic increases in CRABP and CRBP were seen, at both the mRNA and protein levels, during the RA-induced differentiation. CRBP induction differed from that of CRABP in several major ways. 1) Induction of CRBP occurred at lower concentrations of RA (10(-9) M) than did that of CRABP (10(-8)-10(-7) M). 2) CRBP induction was an early response (within 3 h) to RA treatment, whereas CRABP induction occurred at a later time (12-24 h). 3) Induction of CRABP mRNA by RA was blocked by the protein synthesis inhibitor cycloheximide, whereas induction of CRBP mRNA was not. 4) Several differentiation inducers were tested for their effects on the expression of CRABP and CRBP in P19 cells. CRBP induction occurred with a wider spectrum of inducers than did that of CRABP. 5) In addition, the induction of CRABP and CRBP mRNAs by RA was examined in six different cell lines, including three EC lines. CRBP induction occurred in a wider spectrum of cell lines than did that of CRABP. The induction of CRABP in EC cells seems, in general, to correlate with their differentiation into neuron-like cells. Taken together, our results suggest that CRBP induction may be a direct response to RA and represent a general event in RA-induced cell differentiation, whereas CRABP induction may be an indirect response and represent a later event restricted to only certain differentiation pathways. CRBP may be an early response gene induced by RA.
P19胚胎癌细胞可通过用不同浓度的视黄酸(RA)处理在体外诱导分化为多种细胞类型。进行了一项研究以探索在经RA诱导分化的P19细胞中细胞视黄酸结合蛋白(CRABP)和细胞视黄醇结合蛋白(CRBP)基因表达的调控。对于每种类视黄醇结合蛋白,分别通过核糖核酸酶保护分析和特异性放射免疫分析来测量特异性mRNA水平和免疫反应性蛋白水平。在RA诱导的分化过程中,在mRNA和蛋白水平上均观察到CRABP和CRBP显著增加。CRBP的诱导在几个主要方面与CRABP不同。1)CRBP的诱导发生在比CRABP(10^(-8)-10^(-7) M)更低的RA浓度(10^(-9) M)下。2)CRBP的诱导是对RA处理的早期反应(3小时内),而CRABP的诱导发生在较晚时间(12-24小时)。3)RA对CRABP mRNA的诱导被蛋白质合成抑制剂环己酰亚胺阻断,而CRBP mRNA的诱导未被阻断。4)测试了几种分化诱导剂对P19细胞中CRABP和CRBP表达的影响。CRBP的诱导比CRABP的诱导发生在更广泛的诱导剂范围内。5)此外,在包括三种EC细胞系在内的六种不同细胞系中检测了RA对CRABP和CRBP mRNA的诱导。CRBP的诱导发生在比CRABP更广泛的细胞系范围内。一般来说,EC细胞中CRABP的诱导似乎与其向神经元样细胞的分化相关。综上所述,我们的结果表明CRBP的诱导可能是对RA的直接反应,代表RA诱导细胞分化中的一个普遍事件,而CRABP的诱导可能是间接反应,代表仅限于某些分化途径的较晚事件。CRBP可能是由RA诱导的早期反应基因。