1. Mitochondrial clearance of calcium facilitated by MICU2 controls insulin secretion
- Author
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David G. Nicholls, Anya Wernersson, Vamsi K. Mootha, Peter Spégel, Kimberli J. Kamer, H. Barnard, Elaine Cowan, Neelanjan Vishnu, Annika Bagge, Alexander Hamilton, Malin Fex, Anders Tengholm, Hindrik Mulder, and Y. Sancak
- Subjects
0301 basic medicine ,Male ,Voltage-dependent calcium channels ,chemistry.chemical_element ,030209 endocrinology & metabolism ,Mitochondrial calcium uniporter ,Calcium ,Mitochondrion ,Bioenergetics ,03 medical and health sciences ,Mice ,0302 clinical medicine ,Insulin-Secreting Cells ,Insulin Secretion ,Animals ,Humans ,Uniporter ,Inner mitochondrial membrane ,Molecular Biology ,Internal medicine ,Mice, Knockout ,Calcium-Binding Proteins ,Cell Biology ,Hyperpolarization (biology) ,RC31-1245 ,Cell biology ,Mitochondria ,Rats ,Cytosol ,030104 developmental biology ,HEK293 Cells ,chemistry ,Cell culture ,Gene Knockdown Techniques ,Stimulus-secretion coupling ,Mitochondrial Membranes ,Original Article ,Female ,Calcium Channels ,Intracellular ,Knockout mice - Abstract
Objective Transport of Ca2+ into pancreatic β cell mitochondria facilitates nutrient-mediated insulin secretion. However, the underlying mechanism is unclear. Recent establishment of the molecular identity of the mitochondrial Ca2+ uniporter (MCU) and associated proteins allows modification of mitochondrial Ca2+ transport in intact cells. We examined the consequences of deficiency of the accessory protein MICU2 in rat and human insulin-secreting cells and mouse islets. Methods siRNA silencing of Micu2 in the INS-1 832/13 and EndoC-βH1 cell lines was performed; Micu2−/− mice were also studied. Insulin secretion and mechanistic analyses utilizing live confocal imaging to assess mitochondrial function and intracellular Ca2+ dynamics were performed. Results Silencing of Micu2 abrogated GSIS in the INS-1 832/13 and EndoC-βH1 cells. The Micu2−/− mice also displayed attenuated GSIS. Mitochondrial Ca2+ uptake declined in MICU2-deficient INS-1 832/13 and EndoC-βH1 cells in response to high glucose and high K+. MICU2 silencing in INS-1 832/13 cells, presumably through its effects on mitochondrial Ca2+ uptake, perturbed mitochondrial function illustrated by absent mitochondrial membrane hyperpolarization and lowering of the ATP/ADP ratio in response to elevated glucose. Despite the loss of mitochondrial Ca2+ uptake, cytosolic Ca2+ was lower in siMICU2-treated INS-1 832/13 cells in response to high K+. It was hypothesized that Ca2+ accumulated in the submembrane compartment in MICU2-deficient cells, resulting in desensitization of voltage-dependent Ca2+ channels, lowering total cytosolic Ca2+. Upon high K+ stimulation, MICU2-silenced cells showed higher and prolonged increases in submembrane Ca2+ levels. Conclusions MICU2 plays a critical role in β cell mitochondrial Ca2+ uptake. β cell mitochondria sequestered Ca2+ from the submembrane compartment, preventing desensitization of voltage-dependent Ca2+ channels and facilitating GSIS., Graphical abstract Image 1, Highlights • MICU2 deficiency impairs glucose-stimulated insulin secretion. • MICU2 deficiency abrogates mitochondrial calcium uptake. • Depolarization-evoked cytosolic calcium increases are lower in MICU2-deficient cells. • Mitochondria clear calcium from the subplasma membrane region, maintaining calcium influx.
- Published
- 2021