Bioenergetic defects in muscle fibers of RYR1 mutant knock-in mice associated with malignant hyperthermia

• Published in: The Journal of biological chemistry Vol. 295; no. 45; pp. 15226 - 15235
• Main Authors: Chang, Leon, Liu, Xiaochen, Diggle, Christine P., Boyle, John P., Hopkins, Philip M., Shaw, Marie-Anne, Allen, Paul D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06.11.2020; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Bioenergetics; Female; Hyperthermia - genetics; Hyperthermia - metabolism; Male; malignant hyperthermia; Mice; mitochondrial metabolism; mouse; Muscle Fibers, Skeletal - metabolism; muscle physiology; ryanodine receptor; Ryanodine Receptor Calcium Release Channel - genetics; Ryanodine Receptor Calcium Release Channel - metabolism; muscle physiology; mouse; ryanodine receptor; bioenergetics; malignant hyperthermia; mitochondrial metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.RA120.013537

Mutations in the skeletal muscle ryanodine receptor gene (RYR1) can cause susceptibility to malignant hyperthermia (MH), a potentially lethal genetic condition triggered by volatile anesthetics. MH is associated with hypermetabolism, which has directed research interest into oxidative phosphorylation and muscle bioenergetics. The most common cause of MH in the United Kingdom is the c.7300G>A RYR1 variant, which is present in ∼16% of MH families. Our study focuses on the MH susceptible G2435R-RYR1 knock-in mouse model, which is the murine equivalent of the human c.7300G>A genotype. Using a combination of transcriptomics, protein expression, and functional analysis, we investigated adult muscle fiber bioenergetics in this mouse model. RNA-Seq data showed reduced expression of genes associated with mitochondria and fatty acid oxidation in RYR1 mutants when compared with WT controls. Mitochondrial function was assessed by measuring oxygen consumption rates in permeabilized muscle fibers. Comparisons between WT and homozygous G2435R-RYR1 mitochondria showed a significant increase in complex I–facilitated oxidative phosphorylation in mutant muscle. Furthermore, we observed a gene-dose-specific increase in reactive oxygen species production in G2435R-RYR1 muscle fibers. Collectively, these findings provide evidence of metabolic defects in G2435R-RYR1 knock-in mouse muscle under basal conditions. Differences in metabolic profile could be the result of differential gene expression in metabolic pathways, in conjunction with mitochondrial damage accumulated from chronic exposure to increased oxidative stress.