Ozeki A, Tsukamoto I
Department of Food Science and Nutrition, Nara Women's University, Nara 630, Japan.
Biochim Biophys Acta. 1999 Jul 8;1450(3):308-19. doi: 10.1016/s0167-4889(99)00063-4.
Retinoic acid (RA), which was injected within 4 h after partial hepatectomy (PH), inhibited DNA synthesis in regenerating liver. The inhibition was accompanied by apoptosis, evidenced by in situ end labeling and gel electrophoresis of DNA fragmentation. Characteristic DNA fragmentation was obvious at 4 h and reached a maximum at 8 h after injection. Northern blot analysis revealed that RA repressed the expression of c-fos and c-jun at 15 and 30 min with the up-regulation of retinoic acid receptor gamma (RARgamma) and RARbeta at 2 h after PH. The transglutaminase II mRNA level and activity were increased by RA injection at 4 h and 8 h after PH, respectively. The mRNA levels of thymidylate synthase and thymidine kinase, which are rate determining enzymes of DNA synthesis, decreased in RA injected rats. No change was seen in the expression of p53 and p21WAF1/CIP1 which have been suggested to participate in the apoptosis process. These results suggest that RA exerts the antiproliferative activity only on the early stage of liver regeneration accompanied by the repression of c-fos and c-jun expression and induction of apoptosis.
在部分肝切除(PH)后4小时内注射的视黄酸(RA)抑制了再生肝脏中的DNA合成。这种抑制伴随着细胞凋亡,原位末端标记和DNA片段凝胶电泳证明了这一点。特征性DNA片段在注射后4小时明显,在8小时达到最大值。Northern印迹分析显示,PH后2小时,RA在15和30分钟时抑制c-fos和c-jun的表达,同时视黄酸受体γ(RARγ)和RARβ上调。分别在PH后4小时和8小时注射RA可增加转谷氨酰胺酶II的mRNA水平和活性。在注射RA的大鼠中,作为DNA合成限速酶的胸苷酸合成酶和胸苷激酶的mRNA水平降低。在已被认为参与细胞凋亡过程的p53和p21WAF1/CIP1的表达中未观察到变化。这些结果表明,RA仅在肝再生的早期发挥抗增殖活性,伴随着c-fos和c-jun表达的抑制和细胞凋亡的诱导。