生物
内分泌学
内科学
2型糖尿病
胰岛素
糖尿病
重编程
胰岛
葡萄糖稳态
小岛
再生(生物学)
细胞生物学
胰岛素抵抗
细胞
医学
遗传学
作者
Chia‐Wei Cheng,Valentina Villani,Roberta Buono,Min Wei,Sanjeev Kumar,Ömer Yılmaz,Pinchas Cohen,Julie B. Sneddon,Laura Perin,Valter D. Longo
出处
期刊:Cell
[Cell Press]
日期:2017-02-01
卷期号:168 (5): 775-788.e12
被引量:322
标识
DOI:10.1016/j.cell.2017.01.040
摘要
Stem-cell-based therapies can potentially reverse organ dysfunction and diseases, but the removal of impaired tissue and activation of a program leading to organ regeneration pose major challenges. In mice, a 4-day fasting mimicking diet (FMD) induces a stepwise expression of Sox17 and Pdx-1, followed by Ngn3-driven generation of insulin-producing β cells, resembling that observed during pancreatic development. FMD cycles restore insulin secretion and glucose homeostasis in both type 2 and type 1 diabetes mouse models. In human type 1 diabetes pancreatic islets, fasting conditions reduce PKA and mTOR activity and induce Sox2 and Ngn3 expression and insulin production. The effects of the FMD are reversed by IGF-1 treatment and recapitulated by PKA and mTOR inhibition. These results indicate that a FMD promotes the reprogramming of pancreatic cells to restore insulin generation in islets from T1D patients and reverse both T1D and T2D phenotypes in mouse models.PaperClip/cms/asset/f90d7b73-e7d3-4ef8-91a9-9bec91d305c3/mmc2.mp3Loading ...(mp3, 2.35 MB) Download audio
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