Calum Wilson
Mitochondrial ATP production provides long-range control of endothelial inositol trisphosphate–evoked calcium signaling
Wilson, Calum; Lee, Matthew D.; Heathcote, Helen; Zhang, Xun; Buckley, Charlotte; Girkin, John M.; Saunter, Christopher D.; McCarron, John G.
Authors
Matthew D. Lee
Helen Heathcote
Xun Zhang
Charlotte Buckley
Professor John Girkin j.m.girkin@durham.ac.uk
Professor
Christopher D. Saunter
John G. McCarron
Abstract
Endothelial cells are reported to be glycolytic and to minimally rely on mitochondria for ATP generation. Rather than providing energy, mitochondria in endothelial cells may act as signaling organelles that control cytosolic Ca2+ signaling or modify reactive oxygen species (ROS). To control Ca2+ signaling, these organelles are often observed close to influx and release sites and may be tethered near Ca2+ transporters. In this study, we used high-resolution, wide-field fluorescence imaging to investigate the regulation of Ca2+ signaling by mitochondria in large numbers of endothelial cells (~50 per field) in intact arteries from rats. We observed that mitochondria were mostly spherical or form short rod structures and were distributed widely throughout the cytoplasm. The density of these organelles did not increase near contact sites with smooth muscle cells. However, local inositol trisphosphate (IP3)-mediated Ca2+ signaling predominated near these contact sites and required polarized mitochondria. Of note, mitochondrial control of Ca2+ signals occurred even when mitochondria were far from Ca2+ release sites. Indeed, the endothelial mitochondria were mobile and moved throughout the cytoplasm. Mitochondrial control of Ca2+ signaling was mediated by ATP production, which, when reduced by mitochondrial depolarization or ATP synthase inhibition, eliminated local IP3-mediated Ca2+ release events. ROS buffering did not significantly alter local Ca2+ release events. These results highlight the importance of mitochondrial ATP production in providing long-range control of endothelial signaling via IP3-evoked local Ca2+ release in intact endothelium.
Citation
Wilson, C., Lee, M. D., Heathcote, H., Zhang, X., Buckley, C., Girkin, J. M., Saunter, C. D., & McCarron, J. G. (2019). Mitochondrial ATP production provides long-range control of endothelial inositol trisphosphate–evoked calcium signaling. Journal of Biological Chemistry, 294(3), 758-758. https://doi.org/10.1074/jbc.ra118.005913
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 27, 2018 |
Online Publication Date | Nov 29, 2018 |
Publication Date | Jan 31, 2019 |
Deposit Date | Dec 5, 2018 |
Publicly Available Date | Jan 22, 2019 |
Journal | Journal of Biological Chemistry |
Print ISSN | 0021-9258 |
Electronic ISSN | 1083-351X |
Publisher | American Society for Biochemistry and Molecular Biology |
Peer Reviewed | Peer Reviewed |
Volume | 294 |
Issue | 3 |
Pages | 758-758 |
DOI | https://doi.org/10.1074/jbc.ra118.005913 |
Public URL | https://durham-repository.worktribe.com/output/1307699 |
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http://creativecommons.org/licenses/by/4.0/
Copyright Statement
This research was originally published in Wilson, Calum, Lee, Matthew D., Heathcote, Helen, Zhang, Xun, Buckley, Charlotte, Girkin, John M., Saunter, Christopher D. & McCarron, John G. (2019). Mitochondrial ATP production provides long-range control of endothelial inositol trisphosphate–evoked calcium signaling. Journal of Biological Chemistry 294(3): 737-758. Final version published open access under the terms of the Creative Commons CC-BY license.
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