The Lundberg Laboratory for Diabetes Research, Department of Molecular and Clinical Medicine, The Sahlgrenska Academy at University of Gothenburg, 413 45 Gothenburg, Sweden.
Mol Cell Endocrinol. 2012 May 15;355(1):96-105. doi: 10.1016/j.mce.2012.01.024. Epub 2012 Feb 8.
Rapamycin is an immunosuppressive agent used after organ transplantation, but its molecular effects on glucose metabolism needs further evaluation. We explored rapamycin effects on glucose uptake and insulin signalling proteins in adipocytes obtained via subcutaneous (n=62) and omental (n=10) fat biopsies in human donors. At therapeutic concentration (0.01 μM) rapamycin reduced basal and insulin-stimulated glucose uptake by 20-30%, after short-term (15 min) or long-term (20 h) culture of subcutaneous (n=23 and n=10) and omental adipocytes (n=6 and n=7). Rapamycin reduced PKB Ser473 and AS160 Thr642 phosphorylation, and IRS2 protein levels in subcutaneous adipocytes. Additionally, it reduced mTOR-raptor, mTOR-rictor and mTOR-Sin1 interactions, suggesting decreased mTORC1 and mTORC2 formation. Rapamycin also reduced IR Tyr1146 and IRS1 Ser307/Ser616/Ser636 phosphorylation, whereas no effects were observed on the insulin stimulated IRS1-Tyr and TSC2 Thr1462 phosphorylation. This is the first study to show that rapamycin reduces glucose uptake in human adipocytes through impaired insulin signalling and this may contribute to the development of insulin resistance associated with rapamycin therapy.
雷帕霉素是一种在器官移植后使用的免疫抑制剂,但它对葡萄糖代谢的分子作用需要进一步评估。我们探讨了雷帕霉素对人类供体皮下(n=62)和网膜(n=10)脂肪活检中获得的脂肪细胞中葡萄糖摄取和胰岛素信号蛋白的影响。在治疗浓度(0.01 μM)下,雷帕霉素在短期(15 分钟)或长期(20 小时)培养皮下(n=23 和 n=10)和网膜脂肪细胞(n=6 和 n=7)后,减少了基础和胰岛素刺激的葡萄糖摄取 20-30%。雷帕霉素减少了皮下脂肪细胞中 PKB Ser473 和 AS160 Thr642 的磷酸化和 IRS2 蛋白水平。此外,它还减少了 mTOR-raptor、mTOR-rictor 和 mTOR-Sin1 的相互作用,表明 mTORC1 和 mTORC2 的形成减少。雷帕霉素还减少了 IR Tyr1146 和 IRS1 Ser307/Ser616/Ser636 的磷酸化,而对胰岛素刺激的 IRS1-Tyr 和 TSC2 Thr1462 的磷酸化没有影响。这是第一项表明雷帕霉素通过损害胰岛素信号降低人脂肪细胞中葡萄糖摄取的研究,这可能导致与雷帕霉素治疗相关的胰岛素抵抗的发展。