Hsu S L, Lin Y F, Chou C K
Graduate Institute of Microbiology and Immunology, National Yang-Ming Medical College, Taipei, Taiwan, Republic of China.
Biochem J. 1992 Apr 15;283 ( Pt 2)(Pt 2):611-5. doi: 10.1042/bj2830611.
Transferrin and albumin, which are both secreted from the human hepatoma cell line Hep3B, were regulated transcriptionally by retinoic acid (RA) in a dose-dependent manner. The cell growth rate was little affected under the same conditions. The treatment of Hep3B cells with RA (10 microM for 48 h) resulted in an 8-fold increase in transferrin protein synthesis, a 10-fold increase in the steady-state transferrin mRNA level, and a 5-fold increase in its transcriptional rate. The same treatment led to 4-fold decrease in albumin synthesis, as well as a 7-fold decline in the steady-state albumin mRNA level and a 4-fold decrease in the transcriptional rate. Cycloheximide and actinomycin D blocked the action of RA, suggesting that RA may regulate transferrin and albumin gene expression indirectly in human liver cells.
转铁蛋白和白蛋白均由人肝癌细胞系Hep3B分泌,它们受视黄酸(RA)的转录调控,且呈剂量依赖性。在相同条件下,细胞生长速率几乎未受影响。用RA(10微摩尔,处理48小时)处理Hep3B细胞,导致转铁蛋白合成增加8倍,转铁蛋白稳态mRNA水平增加10倍,转录速率增加5倍。相同处理使白蛋白合成减少4倍,白蛋白稳态mRNA水平下降7倍,转录速率降低4倍。环己酰亚胺和放线菌素D阻断了RA的作用,提示RA可能在人肝细胞中间接调控转铁蛋白和白蛋白基因的表达。