| Literature DB >> 28235195 |
Chia-Wei Cheng1, Valentina Villani2, Roberta Buono3, Min Wei4, Sanjeev Kumar5, Omer H Yilmaz6, Pinchas Cohen4, Julie B Sneddon7, Laura Perin2, Valter D Longo8.
Abstract
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.Entities:
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Year: 2017 PMID: 28235195 PMCID: PMC5357144 DOI: 10.1016/j.cell.2017.01.040
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582