Reynolds B, Laynes R, Ogmundsdóttir M H, Boyd C A R, Goberdhan D C I
Department of Physiology, Anatomy and Genetics, Le Gros Clark Building, University of Oxford, South Parks Road, Oxford OX1 3QX, U.K.
Biochem Soc Trans. 2007 Nov;35(Pt 5):1215-7. doi: 10.1042/BST0351215.
The IIS (insulin/IGF (insulin-like growth factor) signalling) cascade has an important role in regulating normal development and physiology, as evidenced by its effects in a host of major human diseases including cancer, Type 2 diabetes and neurodegeneration. Recently, it has become clear that multiple types of local nutrient-sensing mechanisms have an impact on cellular insulin-sensitivity through the downstream kinase TOR (target of rapamycin). In vivo analysis in flies has surprisingly highlighted PATs (proton-assisted amino acid transporters) as having a uniquely potent role in regulating IIS/TOR activity and growth, potentially via a novel signalling mechanism. Other molecules such as the heterodimeric amino acid transporter, CD98, which provides the principal route for cellular uptake of leucine, an amino acid implicated in regulating TOR, also appear to have important effects. As our understanding of how nutrient sensing has an impact on IIS/TOR increases, novel targets to modulate aberrant IIS in disease are likely to emerge, which could complement current strategies designed to block kinases in this pathway.
胰岛素/胰岛素样生长因子(IGF)信号传导级联在调节正常发育和生理过程中起着重要作用,这一点在包括癌症、2型糖尿病和神经退行性疾病在内的许多主要人类疾病中都有体现。最近,很明显多种类型的局部营养感应机制通过下游激酶雷帕霉素靶蛋白(TOR)对细胞胰岛素敏感性产生影响。果蝇体内分析令人惊讶地突出了质子辅助氨基酸转运蛋白(PATs)在调节胰岛素/胰岛素样生长因子信号传导(IIS)/TOR活性和生长方面具有独特的强大作用,这可能是通过一种新的信号传导机制实现的。其他分子,如异二聚体氨基酸转运蛋白CD98,它是细胞摄取亮氨酸(一种与调节TOR有关的氨基酸)的主要途径,似乎也有重要作用。随着我们对营养感应如何影响IIS/TOR的理解不断加深,调节疾病中异常IIS的新靶点可能会出现,这可以补充目前旨在阻断该途径中激酶的策略。