Age-dependent neuromuscular impairment in prion protein knockout mice

Muscle Nerve. 2016 Feb;53(2):269-79. doi: 10.1002/mus.24708. Epub 2015 Nov 26.

Abstract

Introduction: The cellular prion protein (PrP(C) ) is commonly recognized as the precursor of prions, the infectious agents of the fatal transmissible spongiform encephalopathies, or prion diseases. Despite extensive effort, the physiological role of PrP(C) is still ambiguous. Evidence has suggested that PrP(C) is involved in different cellular functions, including peripheral nerve integrity and skeletal muscle physiology.

Methods: We analyzed the age-dependent influence of PrP(C) on treadmill test-based aerobic exercise capacity and on a series of morphological and metabolic parameters using wild-type and genetically modified mice of different ages expressing, or knockout (KO) for, PrP(C) .

Results: We found that aged PrP-KO mice displayed a reduction in treadmill performance compared with PrP-expressing animals, which was associated with peripheral nerve demyelination and alterations of skeletal muscle fiber type.

Conclusion: PrP-KO mice have an age-dependent impairment of aerobic performance as a consequence of specific peripheral nerve and muscle alterations.

Keywords: demyelination; prion protein; sciatic nerve; skeletal muscle; treadmill.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / genetics
  • Adenosine Triphosphatases / metabolism
  • Aging*
  • Animals
  • Citrate (si)-Synthase / metabolism
  • Disease Models, Animal
  • Exercise Test
  • Gene Expression Regulation / genetics
  • Lactic Acid / blood
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Motor Activity / genetics
  • Muscle Fibers, Skeletal / metabolism
  • Muscle Fibers, Skeletal / pathology
  • Muscle Strength / genetics
  • Muscle, Skeletal / physiopathology
  • Myosin Heavy Chains / metabolism
  • Neural Conduction / genetics
  • Neuromuscular Diseases / blood
  • Neuromuscular Diseases / genetics*
  • Neuromuscular Diseases / pathology
  • Neuromuscular Diseases / physiopathology
  • Prions / genetics
  • Prions / metabolism*
  • Sciatic Nerve / pathology
  • Succinate Dehydrogenase / metabolism

Substances

  • Prions
  • Lactic Acid
  • Succinate Dehydrogenase
  • Citrate (si)-Synthase
  • Adenosine Triphosphatases
  • Myosin Heavy Chains