DEC1 regulates human β cell functional maturation and circadian rhythm
Year: 2025
Type: article
Abstract: Stem cell-derived islet (SC-islet) organoids offer hope for cell replacement therapy in diabetes, but their immature function remains a challenge. Mature islet function requires the β cell circadian clock, yet how the clock regulates maturation is unclear. Here, we show that a circadian transcription factor specific to maturing SC-β cells, DEC1, regulates insulin responsiveness to glucose. SC-islet organoids form normally from DEC1-ablated human pluripotent stem cells, but their insulin release capacity and glucose threshold fail to increase during in vitro culture and upon transplant. This deficit reflects the downregulation of maturity-linked effectors of glucose utilization and insulin exocytosis, blunting glycolytic and oxidative metabolism, and is rescued by increasing metabolic flux. Moreover, DEC1 is needed to boost SC-islet maturity by synchronizing circadian glucose-responsive insulin secretion rhythms and clock machinery. Thus, DEC1 links circadian rhythms to human β cell maturation, highlighting the essential role of circadian control in generating fully functional SC-islet organoids.
Source: Cell Reports
Authors: Sam Preza, Bliss Zheng, Zihan Gao, Akshaya Biju, Mai Liu, Zhihui Cheng, Matthew Choi, Juan R. Alvarez-Dominguez
Institution: University of Pennsylvania
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $5,620
Funders: Howard Hughes Medical Institute, University of Pennsylvania, JPB Foundation, Life Sciences Research Foundation, Human Islet Research Network, National Institutes of Health, Perelman School of Medicine, University of Pennsylvania, Diabetes Research Center, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, Institute for Diabetes, Obesity and Metabolism, Perelman School of Medicine, University of Pennsylvania, Division of Diabetes, Endocrinology, and Metabolic Diseases, JDRF
OpenAlex ID: W4417304355
