Rius C, Zorrilla A, Mata F, Aller P
Centro de Investigaciones Biológicas (CSIC), Madrid, Spain.
Biochem Int. 1991 Feb;23(3):555-62.
Administration of 1mM sodium butyrate or N6,2'-O-dibutyryladenosine 3':5'-cyclic monophosphate (dbcAMP) inhibits the growth activity of U937 human monoblastoid cells by blocking them at the G1 or at the G1 + G2 phases of the cell cycle, respectively. Both agents induce the differentiation of U937 cells, as proved by the increased expression of the maturation-associated CD11b antigen and by the increased capacity to reduce nitroblue tetrazolium. RNA blot assays indicate that butyrate and dbcAMP decrease the expression of ornithine decarboxylase and c-myc genes, and stimulate the expression of the vimentin gene. However, while dbcAMP induces c-fos mRNA accumulation, butyrate did not affect the expression of this proto-oncogene.
给予1mM丁酸钠或N6,2'-O-二丁酰腺苷3':5'-环一磷酸(dbcAMP)分别通过将U937人单核细胞样细胞阻滞在细胞周期的G1期或G1 + G2期来抑制其生长活性。两种试剂均诱导U937细胞分化,这通过成熟相关CD11b抗原表达增加以及还原硝基蓝四唑能力增强得以证明。RNA印迹分析表明,丁酸盐和dbcAMP降低鸟氨酸脱羧酶和c-myc基因的表达,并刺激波形蛋白基因的表达。然而,虽然dbcAMP诱导c-fos mRNA积累,但丁酸盐不影响该原癌基因的表达。