SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models

Am J Physiol Cell Physiol. 2015 May 1;308(9):C699-709. doi: 10.1152/ajpcell.00341.2014. Epub 2015 Feb 4.

Abstract

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle wasting secondary to repeated muscle damage and inadequate repair. Elevations in intracellular free Ca²⁺ have been implicated in disease progression, and sarcoplasmic/endoplasmic reticulum Ca²⁺-ATPase 1 (SERCA1) overexpression has been shown to ameliorate the dystrophic phenotype in mdx mice. The purpose of this study was to assess the effects of SERCA1 overexpression in the more severe mdx/Utr(-/-) mouse model of DMD. Mice overexpressing SERCA1 were crossed with mdx/Utr ± mice to generate mdx/Utr(-/-)/+SERCA1 mice and compared with wild-type (WT), WT/+SERCA1, mdx/+SERCA1, and genotype controls. Mice were assessed at ∼12 wk of age for changes in Ca²⁺ handling, muscle mass, quadriceps torque, markers of muscle damage, and response to repeated eccentric contractions. SERCA1-overexpressing mice had a two- to threefold increase in maximal sarcoplasmic reticulum Ca²⁺-ATPase activity compared with WT which was associated with normalization in body mass for both mdx/+SERCA1 and mdx/Utr(-/-)/+SERCA1. Torque deficit in the quadriceps after eccentric injury was 2.7-fold greater in mdx/Utr(-/-) vs. WT mice, but only 1.5-fold greater in mdx/Utr(-/-)/+SERCA1 vs. WT mice, an attenuation of 44%. Markers of muscle damage (% centrally nucleated fibers, necrotic area, and serum creatine kinase levels) were higher in both mdx and mdx/Utr(-/-) vs. WT, and all were attenuated by overexpression of SERCA1. These data indicate that SERCA1 overexpression ameliorates functional impairments and cellular markers of damage in a more severe mouse model of DMD. These findings support targeting intracellular Ca²⁺ control as a therapeutic approach for DMD.

Keywords: Duchenne muscular dystrophy; SERCA1; calcium; injury; mdx; mdx/Utr−/−.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / blood
  • Biomechanical Phenomena
  • Calcium Signaling
  • Creatine Kinase, MM Form / blood
  • Disease Models, Animal
  • Genotype
  • Hypertrophy
  • Mice, Inbred mdx
  • Mice, Transgenic
  • Muscle Contraction*
  • Muscle Strength*
  • Muscular Dystrophy, Duchenne / blood
  • Muscular Dystrophy, Duchenne / enzymology*
  • Muscular Dystrophy, Duchenne / genetics
  • Muscular Dystrophy, Duchenne / pathology
  • Muscular Dystrophy, Duchenne / physiopathology
  • Necrosis
  • Organ Size
  • Phenotype
  • Quadriceps Muscle / enzymology*
  • Quadriceps Muscle / pathology
  • Quadriceps Muscle / physiopathology
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / genetics
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism*
  • Severity of Illness Index
  • Torque
  • Up-Regulation
  • Utrophin / deficiency
  • Utrophin / genetics

Substances

  • Biomarkers
  • Utrophin
  • Creatine Kinase, MM Form
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases