de Juan C, Sánchez A, Nakamura T, Fabregat I, Benito M
Departamento de Bioquímica y Biología Molecular, Centro Mixto C.S.I.C./U.C.M., Facultad de Farmacia, Ciudad Universitaria, Madrid, Spain.
Biochem Biophys Res Commun. 1994 Nov 15;204(3):1364-70. doi: 10.1006/bbrc.1994.2614.
Hepatocyte growth factor (HGF) is a potent mitogen for primary cultured fetal hepatocytes. In the present study, we have analyzed the c-met/HGF receptor expression in fetal hepatocytes and its modulation by growth factors and hormones. 20-day old fetal liver showed a barely expression of c-met mRNA levels. However, when fetal hepatocytes were incubated in the presence of HGF, a 10-fold increase in c-met mRNA levels was observed 30 min after addition of the factor. This HGF-induced effect on c-met expression was transient, losing its up-regulatory effect after 24 hours and returning to the initial levels at 48 hours. Transforming growth factor-beta, a negative regulator of fetal liver growth, increased c-met mRNA levels 48 hours after the addition of the factor, whereas glucocorticoids had a negative effect.
肝细胞生长因子(HGF)是原代培养的胎儿肝细胞的一种强效促有丝分裂剂。在本研究中,我们分析了胎儿肝细胞中c-met/HGF受体的表达及其受生长因子和激素的调节情况。20日龄的胎儿肝脏c-met mRNA水平几乎不表达。然而,当胎儿肝细胞在HGF存在的情况下孵育时,在添加该因子30分钟后观察到c-met mRNA水平增加了10倍。这种HGF诱导的对c-met表达的作用是短暂的,在24小时后失去上调作用,并在48小时回到初始水平。转化生长因子-β是胎儿肝脏生长的负调节因子,在添加该因子48小时后增加c-met mRNA水平,而糖皮质激素则有负面影响。