Rodrigues Michele A, Gomes Dawidson A, Andrade Viviane A, Leite M Fatima, Nathanson Michael H
Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520-8019, USA.
Hepatology. 2008 Nov;48(5):1621-31. doi: 10.1002/hep.22424.
Insulin is an hepatic mitogen that promotes liver regeneration. Actions of insulin are mediated by the insulin receptor, which is a receptor tyrosine kinase. It is currently thought that signaling via the insulin receptor occurs at the plasma membrane, where it binds to insulin. Here we report that insulin induces calcium oscillations in isolated rat hepatocytes, and that these calcium signals depend upon activation of phospholipase C and the inositol 1,4,5-trisphosphate receptor, but not upon extracellular calcium. Furthermore, insulin-induced calcium signals occur in the nucleus, and are temporally associated with selective depletion of nuclear phosphatidylinositol bisphosphate and translocation of the insulin receptor to the nucleus. These findings suggest that the insulin receptor translocates to the nucleus to initiate nuclear, inositol 1,4,5-trisphosphate-mediated calcium signals in rat hepatocytes. This novel signaling mechanism may be responsible for insulin's effects on liver growth and regeneration.
胰岛素是一种促进肝脏再生的肝有丝分裂原。胰岛素的作用由胰岛素受体介导,胰岛素受体是一种受体酪氨酸激酶。目前认为,通过胰岛素受体的信号传导发生在质膜上,胰岛素在质膜上与之结合。在此我们报告,胰岛素可诱导分离的大鼠肝细胞中的钙振荡,并且这些钙信号依赖于磷脂酶C和肌醇1,4,5-三磷酸受体的激活,而不依赖于细胞外钙。此外,胰岛素诱导的钙信号出现在细胞核中,并且在时间上与核磷脂酰肌醇二磷酸的选择性消耗以及胰岛素受体向细胞核的转位相关。这些发现表明,胰岛素受体转位至细胞核以启动大鼠肝细胞中由核内肌醇1,4,5-三磷酸介导的钙信号。这种新的信号传导机制可能是胰岛素对肝脏生长和再生产生作用的原因。