Bernuau D, Moreau A, Tournier I, Legres L, Feldmann G
Laboratoire de Biologie Cellulaire, INSERM U 327, Faculté de Médecine Xavier-Bichat, Paris, France.
Liver. 1993 Apr;13(2):102-9. doi: 10.1111/j.1600-0676.1993.tb00614.x.
Nuclear protooncogene and alpha-fetoprotein gene expression is stimulated in hepatocytes during liver regeneration and by various growth factors in vitro. Metabolic adaptation of hepatocytes has been implicated in such gene reprogrammation. We examine here whether induction of an acute inflammation, a physiological situation of important metabolic adjustments, also triggers activation of nuclear oncogenes and of the AFP gene in rat liver. C-fos, c-jun and c-myc mRNA accumulated on Northern blots between 4-12 h of inflammation and the steady-state level of two small alpha-fetoprotein transcripts characteristic of the adult liver increased at 4 h and 24 h of inflammation. In situ hybridization showed accumulation of the mRNA of the four genes studied in all hepatocytes, without any zonal lobular heterogeneity. 3H-histoautoradiography and mitotic counts indicated an inhibition of DNA synthesis and mitosis, prolonged for at least 48 h after inflammation. Thus acute inflammation triggers the activation of nuclear protooncogenes and alpha-feto-protein gene in hepatocytes, but this activation is not followed by passage into the replicative cycle.
在肝脏再生过程中以及体外多种生长因子作用下,肝细胞中的核原癌基因和甲胎蛋白基因表达会受到刺激。肝细胞的代谢适应与这种基因重编程有关。我们在此研究急性炎症(一种重要代谢调整的生理状况)的诱导是否也会触发大鼠肝脏中核癌基因和甲胎蛋白基因的激活。在炎症发生4 - 12小时之间,C - fos、c - jun和c - myc mRNA在Northern印迹上积累,并且在炎症发生4小时和24小时时,成年肝脏特有的两种小甲胎蛋白转录本的稳态水平升高。原位杂交显示所研究的四个基因的mRNA在所有肝细胞中积累,没有任何小叶带区的异质性。3H - 组织放射自显影和有丝分裂计数表明DNA合成和有丝分裂受到抑制,在炎症后至少持续48小时。因此,急性炎症会触发肝细胞中核原癌基因和甲胎蛋白基因的激活,但这种激活之后不会进入复制周期。