Sharma P M, Egawa K, Gustafson T A, Martin J L, Olefsky J M
Department of Medicine, University of California, San Diego, La Jolla 92093, USA.
Mol Cell Biol. 1997 Dec;17(12):7386-97. doi: 10.1128/MCB.17.12.7386.
Activated insulin receptor (IR) interacts with its substrates, IRS-1, IRS-2, and Shc via the NPXY motif centered at Y960. This interaction is important for IRS-1 phosphorylation. Studies using the yeast two-hybrid system and sequence identity analysis between IRS-1 and IRS-2 have identified two putative elements, the PTB and SAIN domains, between amino acids 108 and 516 of IRS-1 that are sufficient for receptor interaction. However, their precise function in mediating insulin's bioeffects is not understood. We expressed the PTB and SAIN domains of IRS-1 in HIRcB fibroblasts and 3T3-L1 adipocytes utilizing replication-defective adenoviral infection to investigate their role in insulin signalling. In both cell types, overexpression of either the PTB or the SAIN protein caused a significant decrease in insulin-induced tyrosine phosphorylation of IRS-1 and Shc proteins, IRS-1-associated phosphatidylinositol 3-kinase (PI 3-K) enzymatic activity, p70s6k activation, and p44 and p42 mitogen-activated protein kinase (MAPK) phosphorylation. However, epidermal growth factor-induced Shc and MAPK phosphorylation was unaffected by the overexpressed proteins. These findings were associated with a complete inhibition of insulin-stimulated cell cycle progression. In 3T3-L1 adipocytes, PTB or SAIN expression extinguished IRS-1 phosphorylation with a corresponding 90% decrease in IRS-1-associated PI 3-K activity. p70s6k is a downstream target of PI 3-K, and insulin-stimulated p70s6k was inhibited by PTB or SAIN expression. Interestingly, overexpression of either PTB or SAIN protein did not affect insulin-induced AKT activation or insulin-stimulated 2-deoxyglucose transport, even though both of these bioeffects are inhibited by wortmannin. Thus, interference with the IRS-1-IR interaction inhibits insulin-stimulated IRS-1 and Shc phosphorylation, PI 3-K enzymatic activity, p70s6k activation, MAPK phosphorylation and cell cycle progression. In 3T3-L1 adipocytes, interference with the IR-IRS-1 interaction did not cause inhibition of insulin-stimulated AKT activation or glucose transport. These results indicate a bifurcation or subcompartmentalization of the insulin signalling pathway whereby some targets of PI 3-K (i.e., p70s6k) are dependent on IRS-1-associated PI 3-K and other targets (i.e., AKT and glucose transport) are not. IR-IRS-1 interaction is not essential for insulin's effect on glucose transport, and alternate, or redundant, pathways exist in these cells.
活化的胰岛素受体(IR)通过以Y960为中心的NPXY基序与其底物IRS-1、IRS-2和Shc相互作用。这种相互作用对IRS-1磷酸化很重要。利用酵母双杂交系统以及IRS-1和IRS-2之间的序列同一性分析进行的研究,在IRS-1氨基酸108至516之间鉴定出两个假定元件,即PTB和SAIN结构域,它们足以实现受体相互作用。然而,它们在介导胰岛素生物效应中的精确功能尚不清楚。我们利用复制缺陷型腺病毒感染在HIRcB成纤维细胞和3T3-L1脂肪细胞中表达IRS-1的PTB和SAIN结构域,以研究它们在胰岛素信号传导中的作用。在这两种细胞类型中,PTB或SAIN蛋白的过表达均导致胰岛素诱导的IRS-1和Shc酪氨酸磷酸化、与IRS-1相关的磷脂酰肌醇3激酶(PI 3-K)酶活性、p70s6k活化以及p44和p42丝裂原活化蛋白激酶(MAPK)磷酸化显著降低。然而,表皮生长因子诱导的Shc和MAPK磷酸化不受过表达蛋白的影响。这些发现与胰岛素刺激的细胞周期进程的完全抑制相关。在3T3-L1脂肪细胞中,PTB或SAIN的表达消除了IRS-1磷酸化,同时与IRS-1相关的PI 3-K活性相应降低了90%。p70s6k是PI 3-K的下游靶点,胰岛素刺激的p70s6k被PTB或SAIN的表达所抑制。有趣的是,PTB或SAIN蛋白的过表达均不影响胰岛素诱导的AKT活化或胰岛素刺激的2-脱氧葡萄糖转运,尽管这两种生物效应均被渥曼青霉素抑制。因此,干扰IRS-1与IR的相互作用会抑制胰岛素刺激的IRS-1和Shc磷酸化、PI 3-K酶活性、p70s6k活化、MAPK磷酸化以及细胞周期进程。在3T3-L1脂肪细胞中,干扰IR与IRS-1的相互作用不会导致胰岛素刺激的AKT活化或葡萄糖转运受到抑制。这些结果表明胰岛素信号通路存在分支或亚区室化,即PI 3-K的一些靶点(如p70s6k)依赖于与IRS-1相关的PI 3-K,而其他靶点(如AKT和葡萄糖转运)则不依赖。IR与IRS-1的相互作用对于胰岛素对葡萄糖转运的作用并非必不可少,并且在这些细胞中存在替代或冗余途径。