Mouse models for muscular dystrophies: an overview

Dis Model Mech. 2020 Feb 21;13(2):dmm043562. doi: 10.1242/dmm.043562.

Abstract

Muscular dystrophies (MDs) encompass a wide variety of inherited disorders that are characterized by loss of muscle tissue associated with a progressive reduction in muscle function. With a cure lacking for MDs, preclinical developments of therapeutic approaches depend on well-characterized animal models that recapitulate the specific pathology in patients. The mouse is the most widely and extensively used model for MDs, and it has played a key role in our understanding of the molecular mechanisms underlying MD pathogenesis. This has enabled the development of therapeutic strategies. Owing to advancements in genetic engineering, a wide variety of mouse models are available for the majority of MDs. Here, we summarize the characteristics of the most commonly used mouse models for a subset of highly studied MDs, collated into a table. Together with references to key publications describing these models, this brief but detailed overview would be useful for those interested in, or working with, mouse models of MD.

Keywords: Disease pathology; Mouse models; Muscular dystrophy.

Publication types

  • Review

MeSH terms

  • Animals
  • Disease Models, Animal*
  • Gene Targeting
  • Mice
  • Muscular Dystrophies / pathology*
  • Muscular Dystrophies / therapy