Atrophy, oxidative switching and ultrastructural defects in skeletal muscle of the ataxia telangiectasia mouse model

J Cell Sci. 2019 Mar 4;132(5):jcs223008. doi: 10.1242/jcs.223008.

Abstract

Ataxia telangiectasia is a rare, multi system disease caused by ATM kinase deficiency. Atm-knockout mice recapitulate premature aging, immunodeficiency, cancer predisposition, growth retardation and motor defects, but not cerebellar neurodegeneration and ataxia. We explored whether Atm loss is responsible for skeletal muscle defects by investigating myofiber morphology, oxidative/glycolytic activity, myocyte ultrastructural architecture and neuromuscular junctions. Atm-knockout mice showed reduced muscle and fiber size. Atrophy, protein synthesis impairment and a switch from glycolytic to oxidative fibers were detected, along with an increase of in expression of slow and fast myosin types (Myh7, and Myh2 and Myh4, respectively) in tibialis anterior and solei muscles isolated from Atm-knockout mice. Transmission electron microscopy of tibialis anterior revealed misalignments of Z-lines and sarcomeres and mitochondria abnormalities that were associated with an increase in reactive oxygen species. Moreover, neuromuscular junctions appeared larger and more complex than those in Atm wild-type mice, but with preserved presynaptic terminals. In conclusion, we report for the first time that Atm-knockout mice have clear morphological skeletal muscle defects that will be relevant for the investigation of the oxidative stress response, motor alteration and the interplay with peripheral nervous system in ataxia telangiectasia.

Keywords: Atm; Atrophy; Myopathy; ROS; Skeletal muscle; Slow myosin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging, Premature / genetics*
  • Animals
  • Ataxia Telangiectasia / metabolism*
  • Ataxia Telangiectasia / physiopathology
  • Ataxia Telangiectasia Mutated Proteins / genetics*
  • Cells, Cultured
  • Disease Models, Animal
  • Genetic Predisposition to Disease
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microscopy, Electron, Transmission
  • Mitochondria / metabolism*
  • Mitochondria / ultrastructure
  • Muscle, Skeletal / abnormalities
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / ultrastructure
  • Neoplasms / genetics*
  • Reactive Oxygen Species / metabolism
  • Sarcomeres / ultrastructure

Substances

  • Reactive Oxygen Species
  • Ataxia Telangiectasia Mutated Proteins