Tang S J, Ko L W, Lee Y H, Wang F F
Institute of Biochemistry, Yang-Ming Medical College, Taipei, Taiwan, China.
Biochim Biophys Acta. 1990 Jan 30;1048(1):59-65. doi: 10.1016/0167-4781(90)90022-t.
Sodium butyrate has been shown to inhibit the growth and induce the differentiation of F-98 rat glioma cells. In agreement with the morphological changes, we have found that mRNAs for fibronectin and collagen in these cells could be reversibly induced by butyrate. While Ki-ras mRNA levels remained relatively unchanged, mRNAs for fos and sis increased significantly during the course of butyrate induced differentiation. c-fos induction can be detected 30 min after butyrate addition, a peak level (greater than 20 fold) was reached at 2 h, with a subsequent gradual decline. c-sis induction was detectable 24 h after butyrate exposure, at which time the cells have assumed morphological transition. Interestingly, the sis mRNA induction was not reversible upon butyrate withdrawal. The sis mRNA half-life increased from 40 min in the untreated cells to 100 min in the butyrate induced cells indicating that the increase in the stability of sis mRNA contributed, at least in part, to the elevated levels of sis expression. These findings demonstrate a coordinated induction of fibronectin and collagen genes in the butyrate-treated F-98 cells. In addition, fos and sis transcripts were differentially induced; a rapid and transient induction of fos followed by an irreversible induction of sis at a later stage of differentiation.
丁酸钠已被证明可抑制F-98大鼠胶质瘤细胞的生长并诱导其分化。与形态学变化一致,我们发现这些细胞中纤连蛋白和胶原蛋白的mRNA可被丁酸盐可逆性诱导。虽然Ki-ras mRNA水平相对保持不变,但在丁酸盐诱导分化过程中,fos和sis的mRNA显著增加。添加丁酸盐30分钟后可检测到c-fos的诱导,2小时时达到峰值水平(大于20倍),随后逐渐下降。丁酸盐暴露24小时后可检测到c-sis的诱导,此时细胞已发生形态转变。有趣的是,撤去丁酸盐后sis mRNA的诱导不可逆。sis mRNA的半衰期从未经处理的细胞中的40分钟增加到丁酸盐诱导的细胞中的100分钟,这表明sis mRNA稳定性的增加至少部分促成了sis表达水平的升高。这些发现表明在丁酸盐处理的F-98细胞中纤连蛋白和胶原蛋白基因的协同诱导。此外,fos和sis转录本的诱导存在差异;fos快速且短暂的诱导之后是在分化后期sis的不可逆诱导。