An inhibitor-mediated beta-cell dedifferentiation model reveals distinct roles for FoxO1 in glucagon repression and insulin maturation

• Main Authors: Tamara Casteels (Author), Yufeng Zhang (Author), Thomas Frogne (Author), Caterina Sturtzel (Author), Charles-Hugues Lardeau (Author), Ilke Sen (Author), Xiaocheng Liu (Author), Shangyu Hong (Author), Florian M. Pauler (Author), Thomas Penz (Author), Marlene Brandstetter (Author), Charlotte Barbieux (Author), Ekaterine Berishvili (Author), Thomas Heuser (Author), Christoph Bock (Author), Christian G. Riedel (Author), Dirk Meyer (Author), Martin Distel (Author), Jacob Hecksher-Sørensen (Author), Jin Li (Author), Stefan Kubicek (Author)
• Format: Book
• Published: Elsevier, 2021-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Objective: The loss of forkhead box protein O1 (FoxO1) signaling in response to metabolic stress contributes to the etiology of type II diabetes, causing the dedifferentiation of pancreatic beta cells to a cell type reminiscent of endocrine progenitors. Lack of methods to easily model this process i...