Dystrophin-deficient dogs with reduced myostatin have unequal muscle growth and greater joint contractures

• Published in: Skeletal muscle Vol. 6; no. 14; p. 14
• Main Authors: Kornegay, Joe N, Bogan, Daniel J, Bogan, Janet R, Dow, Jennifer L, Wang, Jiahui, Fan, Zheng, Liu, Naili, Warsing, Leigh C, Grange, Robert W, Ahn, Mihye, Balog-Alvarez, Cynthia J, Cotten, Steven W, Willis, Monte S, Brinkmeyer-Langford, Candice, Zhu, Hongtu, Palandra, Joe, Morris, Carl A, Styner, Martin A, Wagner, Kathryn R
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 04.04.2016; BioMed Central
• Subjects: Activin Receptors, Type II - metabolism; Animals; Animals, Genetically Modified; Biomechanical Phenomena; Care and treatment; Contracture - genetics; Contracture - metabolism; Contracture - pathology; Contracture - physiopathology; Disease Models, Animal; Dogs; Duchenne muscular dystrophy; Dystrophin; Dystrophin - deficiency; Dystrophin - genetics; Gait; Genetic aspects; Genetic Predisposition to Disease; Growth; Hybridization, Genetic; Joints - metabolism; Joints - pathology; Joints - physiopathology; Magnetic Resonance Imaging; Muscle Strength; Muscular Dystrophy, Animal - genetics; Muscular Dystrophy, Animal - metabolism; Muscular Dystrophy, Animal - pathology; Muscular Dystrophy, Animal - physiopathology; Myostatin; Myostatin - deficiency; Myostatin - genetics; PAX7 Transcription Factor - metabolism; Phenotype; Posture; Quadriceps Muscle - growth & development; Quadriceps Muscle - metabolism; Quadriceps Muscle - pathology; Satellite Cells, Skeletal Muscle - metabolism; Satellite Cells, Skeletal Muscle - pathology; Whippets; Dogs; Golden retriever muscular dystrophy (GRMD); Myostatin inhibition; Muscle hypertrophy; Contractures; Muscular dystrophy
• ISSN: 2044-5040; 2044-5040
• DOI: 10.1186/s13395-016-0085-7

Myostatin (Mstn) is a negative regulator of muscle growth whose inhibition promotes muscle growth and regeneration. Dystrophin-deficient mdx mice in which myostatin is knocked out or inhibited postnatally have a less severe phenotype with greater total mass and strength and less fibrosis and fatty replacement of muscles than mdx mice with wild-type myostatin expression. Dogs with golden retriever muscular dystrophy (GRMD) have previously been noted to have increased muscle mass and reduced fibrosis after systemic postnatal myostatin inhibition. Based partly on these results, myostatin inhibitors are in development for use in human muscular dystrophies. However, persisting concerns regarding the effects of long-term and profound myostatin inhibition will not be easily or imminently answered in clinical trials. To address these concerns, we developed a canine (GRippet) model by crossbreeding dystrophin-deficient GRMD dogs with Mstn-heterozygous (Mstn (+/-)) whippets. A total of four GRippets (dystrophic and Mstn (+/-)), three GRMD (dystrophic and Mstn wild-type) dogs, and three non-dystrophic controls from two litters were evaluated. Myostatin messenger ribonucleic acid (mRNA) and protein levels were downregulated in both GRMD and GRippet dogs. GRippets had more severe postural changes and larger (more restricted) maximal joint flexion angles, apparently due to further exaggeration of disproportionate effects on muscle size. Flexors such as the cranial sartorius were more hypertrophied on magnetic resonance imaging (MRI) in the GRippets, while extensors, including the quadriceps femoris, underwent greater atrophy. Myostatin protein levels negatively correlated with relative cranial sartorius muscle cross-sectional area on MRI, supporting a role in disproportionate muscle size. Activin receptor type IIB (ActRIIB) expression was higher in dystrophic versus control dogs, consistent with physiologic feedback between myostatin and ActRIIB. However, there was no differential expression between GRMD and GRippet dogs. Satellite cell exhaustion was not observed in GRippets up to 3 years of age. Partial myostatin loss may exaggerate selective muscle hypertrophy or atrophy/hypoplasia in GRMD dogs and worsen contractures. While muscle imbalance is not a feature of myostatin inhibition in mdx mice, findings in a larger animal model could translate to human experience with myostatin inhibitors.