| Literature DB >> 27146011 |
Katleen Lemaire, Lieven Thorrez1, Frans Schuit1.
Abstract
Glucose homeostasis greatly depends on the match between fluctuating insulin demands and adjusted rates of insulin secretion, which is the function of pancreatic beta cells. Emerging evidence suggests that when neonatal beta cells mature, they acquire two faces of differentiated function: an expected "visible face" that depends on specific beta cell proteins needed for regulated insulin release, but also a "hidden face" that represses ubiquitous proteins to prevent inappropriate beta cell function such as elevated basal hormone secretion or insulin release triggered by exercise. This review highlights this novel concept, and we first propose that hidden faces may also be relevant for other specialized tissue functions, such as ketogenesis in the liver. Next, we discuss three scenarios in which aberrant gene expression causes abnormal glucose-induced insulin release and the epigenetic regulation of the hidden face in beta cells. We conclude with perspectives for new research, including beta cell replacement to cure diabetes.Entities:
Keywords: chronic metabolic disease; diabetes; disallowed genes; epigenetic; insulin; repressed genes
Mesh:
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Year: 2016 PMID: 27146011 DOI: 10.1146/annurev-nutr-071715-050808
Source DB: PubMed Journal: Annu Rev Nutr ISSN: 0199-9885 Impact factor: 11.848