Leibiger B, Leibiger I B, Moede T, Kemper S, Kulkarni R N, Kahn C R, de Vargas L M, Berggren P O
The Rolf Luft Center for Diabetes Research, Department of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Mol Cell. 2001 Mar;7(3):559-70. doi: 10.1016/s1097-2765(01)00203-9.
Insulin signaling is mediated by a complex network of diverging and converging pathways, with alternative proteins and isoforms at almost every step in the process. We show here that insulin activates the transcription of its own gene and that of the beta cell glucokinase gene (betaGK) by different mechanisms. Whereas insulin gene transcription is promoted by signaling through insulin receptor A type (Ex11-), PI3K class Ia, and p70s6k, insulin stimulates the betaGK gene by signaling via insulin receptor B type (Ex11+), PI3K class II-like activity, and PKB (c-Akt). Our data provide evidence for selectivity in insulin action via the two isoforms of the insulin receptor, the molecular basis being preferential signaling through different PI3K and protein kinases.
胰岛素信号传导由一个复杂的发散和汇聚途径网络介导,在此过程的几乎每一步都有替代蛋白和异构体。我们在此表明,胰岛素通过不同机制激活其自身基因以及β细胞葡萄糖激酶基因(βGK)的转录。胰岛素基因转录通过胰岛素A型受体(Ex11-)、I a类PI3K和p70s6k信号传导来促进,而胰岛素通过胰岛素B型受体(Ex11+)、II类PI3K样活性和PKB(c-Akt)信号传导来刺激βGK基因。我们的数据为胰岛素通过胰岛素受体的两种异构体发挥作用的选择性提供了证据,其分子基础是通过不同的PI3K和蛋白激酶进行优先信号传导。