Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein

Neuron. 2002 May 16;34(4):521-33. doi: 10.1016/s0896-6273(02)00682-7.

Abstract

alpha-Synucleinopathies are neurodegenerative disorders that range pathologically from the demise of select groups of nuclei to pervasive degeneration throughout the neuraxis. Although mounting evidence suggests that alpha-synuclein lesions lead to neurodegeneration, this remains controversial. To explore this issue, we generated transgenic mice expressing wild-type and A53T human alpha-synuclein in CNS neurons. Mice expressing mutant, but not wild-type, alpha-synuclein developed a severe and complex motor impairment leading to paralysis and death. These animals developed age-dependent intracytoplasmic neuronal alpha-synuclein inclusions paralleling disease onset, and the alpha-synuclein inclusions recapitulated features of human counterparts. Moreover, immunoelectron microscopy revealed that the alpha-synuclein inclusions contained 10-16 nm wide fibrils similar to human pathological inclusions. These mice demonstrate that A53T alpha-synuclein leads to the formation of toxic filamentous alpha-synuclein neuronal inclusions that cause neurodegeneration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Axons / metabolism
  • Axons / pathology
  • Axons / ultrastructure
  • Behavior, Animal / physiology
  • Brain / metabolism*
  • Brain / pathology
  • Brain / ultrastructure
  • Disease Models, Animal
  • Female
  • Gene Expression Regulation / physiology
  • Humans
  • Inclusion Bodies / metabolism*
  • Inclusion Bodies / pathology
  • Inclusion Bodies / ultrastructure
  • Male
  • Mice
  • Mice, Transgenic
  • Microscopy, Electron
  • Movement Disorders / genetics*
  • Movement Disorders / metabolism
  • Movement Disorders / pathology
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Nerve Tissue Proteins / ultrastructure
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / pathology
  • Neurons / metabolism*
  • Neurons / pathology
  • Neurons / ultrastructure
  • Phenotype
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / ultrastructure
  • Solubility
  • Spinal Cord / metabolism*
  • Spinal Cord / pathology
  • Spinal Cord / ultrastructure
  • Synucleins
  • Wallerian Degeneration / genetics
  • Wallerian Degeneration / metabolism
  • Wallerian Degeneration / pathology
  • alpha-Synuclein

Substances

  • Nerve Tissue Proteins
  • Recombinant Fusion Proteins
  • SNCA protein, human
  • Snca protein, mouse
  • Synucleins
  • alpha-Synuclein