Document Type
Article
Publication Date
5-3-2023
Abstract
Calcium transfer into the mitochondrial matrix during sarcoplasmic reticulum (SR) Ca2+ release is essential to boost energy production in ventricular cardiomyocytes (VCMs) and match increased metabolic demand. Mitochondria from female hearts exhibit lower mito-[Ca2+] and produce less reactive oxygen species (ROS) compared to males, without change in respiration capacity. We hypothesized that in female VCMs, more efficient electron transport chain (ETC) organization into supercomplexes offsets the deficit in mito-Ca2+ accumulation, thereby reducing ROS production and stress-induced intracellular Ca2+ mishandling. Experiments using mitochondria-targeted biosensors confirmed lower mito-ROS and mito-[Ca2+] in female rat VCMs challenged with β-adrenergic agonist isoproterenol compared to males. Biochemical studies revealed decreased mitochondria Ca2+ uniporter expression and increased supercomplex assembly in rat and human female ventricular tissues vs male. Importantly, western blot analysis showed higher expression levels of COX7RP, an estrogen-dependent supercomplex assembly factor in female heart tissues vs males. Furthermore, COX7RP was decreased in hearts from aged and ovariectomized female rats. COX7RP overexpression in male VCMs increased mitochondrial supercomplexes, reduced mito-ROS and spontaneous SR Ca2+ release in response to ISO. Conversely, shRNA-mediated knockdown of COX7RP in female VCMs reduced supercomplexes and increased mito-ROS, promoting intracellular Ca2+ mishandling. Compared to males, mitochondria in female VCMs exhibit higher ETC subunit incorporation into supercomplexes, supporting more efficient electron transport. Such organization coupled to lower levels of mito-[Ca2+] limits mito-ROS under stress conditions and lowers propensity to pro-arrhythmic spontaneous SR Ca2+ release. We conclude that sexual dimorphism in mito-Ca2+ handling and ETC organization may contribute to cardioprotection in healthy premenopausal females.
Recommended Citation
Clements, Richard T; Terentyeva, Radmila; Hamilton, Shanna; Janssen, Paul M L; Roder, Karim; Martin, Benjamin Y; Perger, Fruzsina; Schneider, Timothy G; Nichtova, Zuzana; Das, Anindhya S; Veress, Roland; Lee, Beth S; Kim, Do-Gyoon; Koren, Gideon; Stratton, Matthew S; Csordás, György; Accornero, Federica; Belevych, Andriy E; Gyorke, Sandor; and Terentyev, Dmitry, "Sexual Dimorphism in Bidirectional Sr-Mitochondria Crosstalk in Ventricular Cardiomyocytes" (2023). Department of Pathology, Anatomy, and Cell Biology Faculty Papers. Paper 395.
https://jdc.jefferson.edu/pacbfp/395
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
37138037
Language
English
Comments
This article is the author's final published version in Basic Research in Cardiology, Volume 118, Issue 1, 2023, Article number 15.
The published version is available at https://doi.org/10.1007/s00395-023-00988-1.
Copyright © The Author(s) 2023
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