Division of Pediatric Surgery, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15224, USA.
Department of General Surgery, Shanghai Children's Hospital, Shanghai Jiao Tong University, No. 355, Luding Rd, Shanghai, 200062, China.
Sci Rep. 2017 Nov 27;7(1):16348. doi: 10.1038/s41598-017-16485-0.
Autophagy is a major regulator of pancreatic beta cell homeostasis. Altered autophagic activity has been implicated in the beta cells of patients with type 2 diabetes, and in the beta cells of obese diabetic rodents. Here, we show that autophagy was induced in beta cells by either a high-fat diet or a combined high-fat and high-glucose diet, but not by high-glucose alone. However, a high-glucose intake alone did increase beta cell mass and insulin secretion moderately. Depletion of Atg7, a necessary component of the autophagy pathway, in beta cells by pancreatic intra-ductal AAV8-shAtg7 infusion in C57BL/6 mice, resulted in decreased beta cell mass, impaired glucose tolerance, defective insulin secretion, and increased apoptosis when a combined high-fat and high-glucose diet was given, seemingly due to suppression of autophagy. Taken together, our findings suggest that the autophagy pathway may act as a protective mechanism in pancreatic beta cells during a high-calorie diet.
自噬是胰腺β细胞稳态的主要调节者。改变自噬活性与 2 型糖尿病患者的β细胞以及肥胖型糖尿病啮齿动物的β细胞有关。在这里,我们发现高脂肪饮食或高脂肪和高葡萄糖饮食均可诱导β细胞发生自噬,但单独的高葡萄糖则不能。然而,单独的高葡萄糖摄入确实适度增加了β细胞的质量和胰岛素分泌。在 C57BL/6 小鼠的胰腺内导管 AAV8-shAtg7 输注中,通过β细胞耗竭自噬途径的必需成分 Atg7,当给予高脂肪和高葡萄糖饮食时,β细胞质量减少、葡萄糖耐量受损、胰岛素分泌缺陷和细胞凋亡增加,这似乎是由于自噬受到抑制。总之,我们的研究结果表明,自噬途径在高热量饮食期间可能作为胰腺β细胞的一种保护机制。