Kubota N, Tobe K, Terauchi Y, Eto K, Yamauchi T, Suzuki R, Tsubamoto Y, Komeda K, Nakano R, Miki H, Satoh S, Sekihara H, Sciacchitano S, Lesniak M, Aizawa S, Nagai R, Kimura S, Akanuma Y, Taylor S I, Kadowaki T
Department of Metabolic Disease, Graduate School of Medicine, University of Tokyo, Japan.
Diabetes. 2000 Nov;49(11):1880-9. doi: 10.2337/diabetes.49.11.1880.
To investigate the role of insulin receptor substrate (IRS)-2 in vivo, we generated IRS-2-deficient mice by gene targeting. Although homozygous IRS-2-deficient mice (IRS-2-/- mice) had a body weight similar to wild-type mice, they progressively developed type 2 diabetes at 10 weeks. IRS-2-/- mice showed insulin resistance and a defect in the insulin-stimulated signaling pathway in liver but not in skeletal muscle. Despite insulin resistance, the amount of beta-cells was reduced to 83% of that in wild-type mice, which was in marked contrast to the 85% increase in the amount of beta-cells in IRS-1-deficient mice (IRS-1-/- mice) to compensate for insulin resistance. Thus, IRS-2 plays a crucial role in the regulation of beta-cell mass. On the other hand, insulin secretion by the same number of cells in response to glucose measured ex vivo was significantly increased in IRS-2-/- mice compared with wild-type mice but was decreased in IRS-1-/- mice. These results suggest that IRS-1 and IRS-2 may play different roles in the regulation of beta-cell mass and the function of individual beta-cells.
为了研究胰岛素受体底物(IRS)-2在体内的作用,我们通过基因打靶技术培育出IRS-2基因缺陷小鼠。尽管纯合子IRS-2基因缺陷小鼠(IRS-2-/-小鼠)的体重与野生型小鼠相似,但它们在10周龄时逐渐发展为2型糖尿病。IRS-2-/-小鼠表现出胰岛素抵抗,且肝脏中胰岛素刺激的信号通路存在缺陷,但骨骼肌中没有。尽管存在胰岛素抵抗,但β细胞数量减少至野生型小鼠的83%,这与IRS-1基因缺陷小鼠(IRS-1-/-小鼠)中β细胞数量增加85%以代偿胰岛素抵抗形成显著对比。因此,IRS-2在β细胞量的调节中起关键作用。另一方面,与野生型小鼠相比,体外测量时IRS-2-/-小鼠中相同数量的细胞对葡萄糖刺激的胰岛素分泌显著增加,而IRS-1-/-小鼠中则减少。这些结果表明,IRS-1和IRS-2在β细胞量的调节以及单个β细胞的功能中可能发挥不同作用。