Vitamin K-dependent carboxylation regulates Ca2+ flux and adaptation to metabolic stress in β cells
Vitamin K is a micronutrient necessary for γ-carboxylation of glutamic acids. This post-translational modification occurs in the endoplasmic reticulum (ER) and affects secreted proteins. Recent clinical studies implicate vitamin K in the pathophysiology of diabetes, but the underlying molecular mech...
Saved in:
Published in | Cell reports (Cambridge) Vol. 42; no. 5; p. 112500 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
30.05.2023
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Vitamin K is a micronutrient necessary for γ-carboxylation of glutamic acids. This post-translational modification occurs in the endoplasmic reticulum (ER) and affects secreted proteins. Recent clinical studies implicate vitamin K in the pathophysiology of diabetes, but the underlying molecular mechanism remains unknown. Here, we show that mouse β cells lacking γ-carboxylation fail to adapt their insulin secretion in the context of age-related insulin resistance or diet-induced β cell stress. In human islets, γ-carboxylase expression positively correlates with improved insulin secretion in response to glucose. We identify endoplasmic reticulum Gla protein (ERGP) as a γ-carboxylated ER-resident Ca2+-binding protein expressed in β cells. Mechanistically, γ-carboxylation of ERGP protects cells against Ca2+ overfilling by diminishing STIM1 and Orai1 interaction and restraining store-operated Ca2+ entry. These results reveal a critical role of vitamin K-dependent carboxylation in regulation of Ca2+ flux in β cells and in their capacity to adapt to metabolic stress.
[Display omitted]
•Vitamin K-dependent carboxylation regulates glucose-stimulated insulin secretion•ERGP is a γ-carboxylated protein controlling store-operated calcium entry•ERGP γ-carboxylation reduces STIM1 and Orai1 puncta formation•Decarboxylated ERGP causes calcium overfilling in β cells and hyperinsulinemia
Reduced vitamin K (VK) intake is associated with an increased risk of developing type 2 diabetes. Lacombe et al. demonstrate that VK-dependent carboxylation is necessary for β cell adaptation in mice fed a high-fat diet. The underlying mechanism involves ERGP, a carboxylated protein that regulates store-operated calcium entry in β cells. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 AUTHOR CONTRIBUTIONS J.L. and M.F. conceived the study, designed the experiments, and initiated the project. J.L., K.G., D.F. and M.F. collected and analyzed data. J.B., F.G., S.M.M., and S.H. collected data. A.V. and V.P. prepared islet cDNA from rats infused with glucose. M.F. and J.L. wrote the manuscript, and all authors commented and contributed to editing the final version. M.F. acts as the guarantor of this work and is responsible for data access. |
ISSN: | 2211-1247 2211-1247 |
DOI: | 10.1016/j.celrep.2023.112500 |