Mitochondrial morphology regulates organellar Ca2+ uptake and changes cellular Ca2+ homeostasis. Issue 12 (5th September 2019)

• Record Type: Journal Article
• Authors: Kowaltowski, Alicia J.; Menezes‐Filho, Sergio L.; Assali, Essam A.; Gonçalves, Isabela G.; Cabral‐Costa, João Victor; Abreu, Phablo; Miller, Nathanael; Nolasco, Patricia; Laurindo, Francisco R. M.; Bruni‐Cardoso, Alexandre; Shirihai, Orian S.
• Is Part Of: FASEB journal. Volume 33:Issue 12(2019)
• Page Start: 13176
• Page End: 13188
• Publication Date: 2019-09-05
• Subjects: mitochondria -- calcium -- ER stress -- metabolism -- bioenergetics; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201901136R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Changes in mitochondrial size and shape have been implicated in several physiologic processes, but their role in mitochondrial Ca 2+ uptake regulation and overall cellular Ca 2+ homeostasis is largely unknown. Here we show that modulating mitochondrial dynamics toward increased fusion through expression of a dominant negative (DN) form of the fission protein [dynamin‐related protein 1 (DRP1)] markedly increased both mitochondrial Ca 2+ retention capacity and Ca 2+ uptake rates in permeabilized C2C12 cells. Similar results were seen using the pharmacological fusion‐promoting M1 molecule. Conversely, promoting a fission phenotype through the knockdown of the fusion protein mitofusin (MFN)‐2 strongly reduced the mitochondrial Ca 2+ uptake speed and capacity in these cells. These changes were not dependent on modifications in mitochondrial calcium uniporter expression, inner membrane potentials, or the mitochondrial permeability transition. Implications of mitochondrial morphology modulation on cellular calcium homeostasis were measured in intact cells; mitochondrial fission promoted lower basal cellular calcium levels and lower endoplasmic reticulum (ER) calcium stores, as indicated by depletion with thapsigargin. Indeed, mitochondrial fission was associated with ER stress. Additionally, the calcium‐replenishing process of store‐operated calcium entry was impaired in MFN2 knockdown cells, whereas DRP1‐DN‐promoted fusion resulted in faster cytosolic Ca 2+ increase rates. Overall, our results show a novel role for mitochondrial morphology in the regulation of mitochondrial Ca 2+ uptake, which impacts cellular Ca 2+ homeostasis.—Kowaltowski, A. J., Menezes‐Filho, S. L., Assali, E. A., Gonçalves, I. G., Cabral‐Costa, J. V., Abreu, P., Miller, N., Nolasco, P., Laurindo, F. R. M., Bruni‐Cardoso, A., Shirihai, O. Mitochondrial morphology regulates organellar Ca 2+ uptake and changes cellular Ca 2+ homeostasis. FASEB J. 33, 13176–13188 (2019). www.fasebj.org