Autophagy protects pancreatic beta cell mass and function in the setting of a high-fat and high-glucose diet

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作者
Qingfeng Sheng
Xiangwei Xiao
Krishna Prasadan
Congde Chen
Yungching Ming
Joseph Fusco
Nupur N. Gangopadhyay
David Ricks
George K. Gittes
机构
[1] Division of Pediatric Surgery,
[2] Children’s Hospital of Pittsburgh,undefined
[3] University of Pittsburgh School of Medicine,undefined
[4] Department of General Surgery,undefined
[5] Shanghai Children’s Hospital,undefined
[6] Shanghai Jiao Tong University,undefined
[7] No. 355,undefined
[8] Luding Rd,undefined
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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.
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