Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Universityof Alabama at Birmingham Comprehensive Diabetes Center, AL 35294, USA.
Am J Physiol Endocrinol Metab. 2012 Jan 15;302(2):E201-8. doi: 10.1152/ajpendo.00497.2011. Epub 2011 Oct 25.
Elevated tissue levels of angiotensin II (ANG II) are associated with impairment of insulin actions in metabolic and cardiovascular tissues. ANG II-stimulated activation of mammalian target of rapamycin (mTOR)/p70 S6 kinase (p70S6K) in cardiovascular tissues is implicated in cardiac hypertrophy and vascular remodeling. However, the role of ANG II-stimulated mTOR/p70S6K in vascular endothelium is poorly understood. In the present study, we observed that ANG II stimulated p70S6K in bovine aortic endothelial cells. ANG II increased phosphorylation of insulin receptor substrate-1 (IRS-1) at Ser(636/639) and inhibited the insulin-stimulated phosphorylation of endothelial nitric oxide synthase (eNOS). An inhibitor of mTOR, rapamycin, attenuated the ANG II-stimulated phosphorylation of p70S6K and phosphorylation of IRS-1 (Ser(636/639)) and blocked the ability of ANG II to impair insulin-stimulated phosphorylation of eNOS, nitric oxide production, and mesenteric-arteriole vasodilation. Moreover, point mutations of IRS-1 at Ser(636/639) to Ala prevented the ANG II-mediated inhibition of insulin signaling. From these results, we conclude that activation of mTOR/p70S6K by ANG II in vascular endothelium may contribute to impairment of insulin-stimulated vasodilation through phosphorylation of IRS-1 at Ser(636/639). This ANG II-mediated impairment of vascular actions of insulin may help explain the role of ANG II as a link between insulin resistance and hypertension.
血管紧张素 II(ANG II)组织水平升高与代谢和心血管组织中胰岛素作用受损有关。在心血管组织中,ANG II 刺激哺乳动物雷帕霉素靶蛋白(mTOR)/p70 S6 激酶(p70S6K)的激活与心脏肥大和血管重塑有关。然而,ANG II 刺激的 mTOR/p70S6K 在血管内皮中的作用知之甚少。在本研究中,我们观察到 ANG II 刺激牛主动脉内皮细胞中的 p70S6K。ANG II 增加胰岛素受体底物-1(IRS-1)丝氨酸(636/639)的磷酸化,并抑制胰岛素刺激的内皮型一氧化氮合酶(eNOS)的磷酸化。mTOR 的抑制剂雷帕霉素减弱了 ANG II 刺激的 p70S6K 和 IRS-1(Ser636/639)磷酸化,并阻断了 ANG II 损害胰岛素刺激的 eNOS 磷酸化、一氧化氮产生和肠系膜小动脉舒张的能力。此外,IRS-1 丝氨酸(636/639)点突变至丙氨酸可防止 ANG II 介导的胰岛素信号抑制。从这些结果中,我们得出结论,ANG II 在血管内皮中激活 mTOR/p70S6K 可能通过 IRS-1 丝氨酸(636/639)的磷酸化导致胰岛素刺激的血管舒张受损。这种 ANG II 介导的胰岛素血管作用损害可能有助于解释 ANG II 作为胰岛素抵抗和高血压之间联系的作用。