Junctional membrane Ca<sup>2+</sup> dynamics in human muscle fibers are altered by malignant hyperthermia causative RyR mutation.
basic_science · Level V
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- Record sourced from PubMed, PMID 30038012.
- Also identified by DOI 10.1073/pnas.1800490115 and PMC identifier 6094124.
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Abstract
We used the nanometer-wide tubules of the transverse tubular (t)-system of human skeletal muscle fibers as sensitive sensors for the quantitative monitoring of the Ca<sup>2+</sup>-handling properties in the narrow junctional cytoplasmic space sandwiched between the tubular membrane and the sarcoplasmic reticulum cisternae in single muscle fibers. The t-system sealed with a Ca<sup>2+</sup>-sensitive dye trapped in it is sensitive to changes in ryanodine receptor (RyR) Ca<sup>2+</sup> leak, the store operated calcium entry flux, plasma membrane Ca pump, and sodium-calcium exchanger activities, thus making the sealed t-system a nanodomain Ca<sup>2+</sup> sensor of Ca<sup>2+</sup> dynamics in the junctional space. The sensor was used to assess the basal Ca<sup>2+</sup>-handling properties of human muscle fibers obtained by needle biopsy from control subjects and from people with a malignant hyperthermia (MH) causative RyR variant. Using this approach we show that the muscle fibers from MH-susceptible individuals display leakier RyRs and a greater capacity to extrude Ca<sup>2+</sup> across the t-system membrane compared with fibers from controls. This study provides a quantitative way to assess the effect of RyR variants on junctional membrane Ca<sup>2+</sup> handling under defined ionic conditions.
Medical subject headings
- Calcium
- Intercellular Junctions
- Malignant Hyperthermia
- Ryanodine Receptor Calcium Release Channel
- Sarcoplasmic Reticulum