Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Ann N Y Acad Sci. 2010 Jul;1201:79-83. doi: 10.1111/j.1749-6632.2010.05614.x.
Type 2 diabetes mellitus is characterized by insulin resistance and failure of pancreatic beta-cells producing insulin. Mitochondrial dysfunction may play a role in both processes of diabetes. Autophagy maintains cellular homeostasis through degradation and recycling of organelles such as mitochondria. As dysfunctional mitochondria are the main organelles removed by autophagy, we studied the role of autophagy in diabetes using mice with beta-cell-specific deletion of the Atg7 gene. Atg7-mutant mice showed reduction in beta-cell mass and pancreatic insulin content. Electron microscopy showed swollen mitochondria and other ultrastructural changes in autophagy-deficient beta-cells. Insulin secretory function ex vivo was also impaired. As a result, Atg7-mutant mice showed hypoinsulinemia and hyperglycemia. These results suggest that autophagy is necessary to maintain structure, mass, and function of beta-cells. Besides its effect on beta-cells, autophagy may affect insulin sensitivity because mitochondrial dysfunction has been implicated in insulin resistance and autophagy is involved in the maintenance of the organelles. Furthermore, since aging is associated with impaired glucose tolerance, decline of autophagic activity may be involved in age-associated reduction of glucose tolerance.
2 型糖尿病的特征为胰岛素抵抗和胰腺β细胞产生胰岛素的功能衰竭。线粒体功能障碍可能在糖尿病的这两个过程中都发挥作用。自噬通过降解和回收细胞器(如线粒体)来维持细胞内稳态。由于功能失调的线粒体是自噬主要清除的细胞器,我们使用胰岛β细胞特异性敲除 Atg7 基因的小鼠来研究自噬在糖尿病中的作用。Atg7 突变小鼠的β细胞数量和胰腺胰岛素含量减少。电镜显示自噬缺陷的β细胞中线粒体肿胀和其他超微结构改变。体外胰岛素分泌功能也受损。因此,Atg7 突变小鼠出现胰岛素血症和高血糖。这些结果表明自噬对于维持β细胞的结构、质量和功能是必需的。除了对β细胞的作用外,自噬可能影响胰岛素敏感性,因为线粒体功能障碍与胰岛素抵抗有关,而自噬参与细胞器的维持。此外,由于衰老与葡萄糖耐量受损相关,自噬活性的下降可能与年龄相关的葡萄糖耐量降低有关。