Fiche publication
Date publication
septembre 2018
Journal
Diabetes, obesity & metabolism
Auteurs
Membres identifiés du Cancéropôle Est :
Pr RICCI Roméo
Tous les auteurs :
Mészáros G, Pasquier A, Vivot K, Goginashvili A, Ricci R
Lien Pubmed
Résumé
Regulated insulin secretion from pancreatic β-cells is a major process maintaining glucose homeostasis in mammals. Enhancing insulin release in response to chronic nutrient overload and obesity-related insulin resistance (pre-diabetes) requires several adaptive cellular mechanisms maintaining β-cell health under such stresses. Once these mechanisms are overwhelmed, β-cell failure occurs leading to full-blown Type 2 Diabetes (T2D). Nutrient-dependent macroautophagy represents one such adaptive mechanism in β-cells. While macroautophagy levels are high and protective in β-cells in pre-diabetes, they decrease at later stages contributing to β-cell failure. However, mechanisms compromising macroautophagy in β-cells remain poorly understood. In this review, we discuss how recently discovered signalling cascades that emanate from the limiting membrane of lysosomes contribute to changes in macroautophagy flux in physiology and disease. In particular, these mechanisms are put into context with β-cell function highlighting most recently described links between nutrient-dependent lysosomal signalling pathways and insulin secretion. Understanding these mechanisms in response to metabolic stress might pave the way for development of more tailored treatment strategies aimed at preserving β-cell health.
Mots clés
AMPK, lysosomal degradation of insulin granules, lysosome, mTORC1, macroautophagy, pancreatic β-cell, protein kinase D1
Référence
Diabetes Obes Metab. 2018 Sep;20 Suppl 2:104-115
