Litcius/Paper detail

Muscle-specific Ryanodine receptor 1 properties underlie limb-girdle muscular dystrophy 2B/R2 progression

Aldo Meizoso‐Huesca, C. R. Lamboley, James R. Krycer, Mark P. Hodson, James E. Hudson, Bradley S. Launikonis

2025Nature Communications9 citationsDOIOpen Access PDF

Abstract

Ryanodine receptor 1 Ca2+ leak is a signal in skeletal muscle, but chronic leak can underlie pathology. Here we show that in healthy male mouse, limb-girdle muscle presents higher sympathetic input, elevated ryanodine receptor 1 basal phosphorylation, Ca2+ leak and mitochondrial Ca2+ content compared to distal leg muscles. These regional differences are consistent with heat generation in resting muscle to maintain core temperature. The dysferlin-null mouse develops severe pathology in the limb-girdle but not leg muscles. Absence of dysferlin disrupts dihydropyridine receptors’ inhibitory control over ryanodine receptor 1 leak, synergistically increasing leak through the already phosphorylated channel of limb-girdle muscle. This alters Ca2+ handling and distribution leading to reactive oxygen species production prior to disease onset. With age, oxidation of Ca2+ -handling proteins in dysferlin-null limb-girdle muscle alters basal Ca2+ movements. Our results show that muscle-specific pathology in dysferlin-null mice is linked to increased ryanodine receptor 1 Ca2+ leak. In this study by Meizoso-Huesca et al. regional skeletal muscle differences in ryanodine receptor Ca2+ leak were found. Without dysferlin, this raised leak is not tolerated long-term and leads to limbgirdle muscular dystrophy in mice.

Topics & Concepts

Ryanodine receptorLimb-girdle muscular dystrophyMuscular dystrophyAnatomyBiologyMedicineReceptorGeneticsMutationGeneAdipose Tissue and MetabolismMuscle Physiology and DisordersExercise and Physiological Responses