Year: 2020
Type: article
Abstract: Summary The orosomucoid-like proteins (Ormdl1-3) are emerging as the critical regulators of sphingolipid homeostasis, inflammation and ER stress. However, their roles in β-cells and obesity remain unknown. Here, we showed that islets isolated from overweight/obese human donors displayed marginally reduced ORMDL1-2 expression while ORMDL3 expression was significantly reduced as compared to islets from lean donors. In contrast, Ormdl3 expression was significantly upregulated in the islets of leptin-deficient obese (ob/ob) mice compared to lean mice. We identified that the difference in expression of Ormdl3 between mouse and human islets was leptin-dependent, as treatment of ob / ob mice with leptin significantly reduced Ormld3 expression. Furthermore, Ormdl1-3 were significantly upregulated upon chemically-induced ER stress, but they showed differential responsiveness to cytokines in a β-cell line. Knockdown of Ormdl3 substantially increased expression of apoptotic markers, which was rescued by a pharmacological inhibitor of ceramide synthase. Taken together we demonstrate leptin-dependent regulation of Ormdl3 expression in ob/ob islets, highlight the possible importance of β-cell stress conditions in differential Ormdl expression and identify a critical role for Ormdl3 in β-cell survival.
Source: iScience
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,000
Awards: G1006252648, G1500003935, G194065125, G2200747520, G2225492, G3122074085, G4700428050, G5124069177, G5520316217, G5604692135, G6148957032, Graduate Training in Molecular Biosciences, Beta cell endoplasmic reticulum stress and its crosstalk with immune system in ty, Role of inhibitory G protein signaling in regulating beta-cell function and survival in the type 1 diabetic state, G9000048659, G9000059835, G9000298918, G924093365
OpenAlex ID: W3038058327
