The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy

<jats:title>Abstract</jats:title><jats:p>Duchenne muscular dystrophy (DMD) is an X-linked, lethal muscle degenerative disease caused by loss of dystrophin protein. DMD has no cure and few treatment options. Preclinical efforts to identify potential DMD therapeutics have been hampered by lack of a small animal model that recapitulates key features of the human disease. While the dystrophin-deficient <jats:italic>mdx</jats:italic> mouse on the C57BL/10 genetic background (B10.<jats:italic>mdx</jats:italic>) is mildly affected, a more severe muscle disease is observed when the <jats:italic>mdx</jats:italic> mutation is crossed onto the DBA/2J genetic background (D2.<jats:italic>mdx</jats:italic>). In this study, the functional and histological progression of the D2.<jats:italic>mdx</jats:italic> skeletal muscle pathology was evaluated to determine the distinguishing features of disease. Data herein details the muscular weakness and wasting exhibited by D2.<jats:italic>mdx</jats:italic> skeletal muscle, as well as severe histopathological features, which include the rapid progression of fibrosis and calcifications in the diaphragm and progressive fibrosis accumulation in limb muscles. Furthermore, a timeline of D2.<jats:italic>mdx</jats:italic> progression is provided that details distinct stages of disease progression. These data support the D2.<jats:italic>mdx</jats:italic> as a superior small animal model for DMD, as compared to the B10.<jats:italic>mdx</jats:italic> model. The insights provided in this report should facilitate the design of preclinical evaluations for potential DMD therapeutics.</jats:p>