Gianni M, Studer M, Carpani G, Terao M, Garattini E
Molecular Biology Unit, Centro Daniela e Catullo Borgomainerio, Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Biochem J. 1991 Mar 15;274 ( Pt 3)(Pt 3):673-8. doi: 10.1042/bj2740673.
All-trans retinoic acid (RA) induces alkaline phosphatase (ALP) activity by 3-8-fold in murine F9 teratocarcinoma cells, in parallel with their differentiation towards primitive endoderm. The elevation of ALP activity is associated with increases in the amounts of liver/bone/kidney-type ALP protein and the respective transcript. These effects of RA are due to activation of ALP gene transcription rather than to an increase in the half-life of the mRNA. Induction of ALP mRNA does not require de novo protein synthesis, since it is not blocked by treatment with cycloheximide. Dibutyryl cyclic AMP, which is known to induce further differentiation of F9 cells from the primitive to the parietal endoderm, blocks the induction of ALP mRNA by RA.
全反式维甲酸(RA)可使小鼠F9畸胎瘤细胞中的碱性磷酸酶(ALP)活性提高3至8倍,同时这些细胞会向原始内胚层分化。ALP活性的升高与肝/骨/肾型ALP蛋白及相应转录本数量的增加有关。RA的这些作用是由于ALP基因转录的激活,而非mRNA半衰期的延长。ALP mRNA的诱导不需要从头合成蛋白质,因为用环己酰亚胺处理不会阻断它。已知二丁酰环磷酸腺苷可诱导F9细胞从原始内胚层进一步分化为滋养层内胚层,它会阻断RA对ALP mRNA的诱导。