Shao Q, Arakaki N, Ohnishi T, Nakamura O, Daikuhara Y
Department of Biochemistry, Kagoshima University Dental School.
J Biochem. 1996 May;119(5):940-6. doi: 10.1093/oxfordjournals.jbchem.a021333.
Hepatocyte growth factor (HGF)/scatter factor is known to be the most potent mitogen for hepatocytes. In this paper, we report that lipogenesis in primary cultured rat hepatocytes treated with 10 ng/ml of recombinant human HGF (rhHGF) for 24 h was stimulated, as measured by the incorporation of 3H2O into long-chain fatty acids, to more than twice as much as the control. Insulin (0.1 microM) was more effective than rhHGF but rhHGF did not show an additive or synergistic effect when added to insulin. We also showed that treatment with rhHGF increased the activities of glucose-6-phosphate dehydrogenase (G6PDH) and malic enzyme, key enzymes which supply NADPH for lipogenesis, and acetyl-CoA carboxylase, the rate-limiting enzyme of lipogenesis. The increase in G6PDH and acetyl-CoA carboxylase activities was accompanied by increases in the levels of mRNA for the enzymes. These results suggest that HGF is involved in liver regeneration not only by stimulation of cell proliferation but also by acceleration of differentiation of hepatocytes.
肝细胞生长因子(HGF)/分散因子是已知对肝细胞最有效的促有丝分裂原。在本文中,我们报道,用10 ng/ml重组人HGF(rhHGF)处理原代培养的大鼠肝细胞24小时后,通过3H2O掺入长链脂肪酸来测定,脂肪生成受到刺激,比对照增加了两倍多。胰岛素(0.1 microM)比rhHGF更有效,但当与胰岛素一起添加时,rhHGF未显示出相加或协同作用。我们还表明,用rhHGF处理可增加葡萄糖-6-磷酸脱氢酶(G6PDH)和苹果酸酶的活性,这两种关键酶为脂肪生成提供NADPH,以及脂肪生成的限速酶乙酰辅酶A羧化酶。G6PDH和乙酰辅酶A羧化酶活性的增加伴随着这些酶的mRNA水平的增加。这些结果表明,HGF不仅通过刺激细胞增殖参与肝脏再生,还通过加速肝细胞分化参与肝脏再生。