4.5 Article

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3

期刊

HUMAN MOLECULAR GENETICS
卷 18, 期 5, 页码 942-955

出版社

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddn422

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资金

  1. RIKEN BSI,
  2. Ministry of Education, Culture, Sports, Science and Technology, NIBIO
  3. Japan Foundation for Neuroscience and Mental Health
  4. Ministry of Health, Labor and Welfare of Japan
  5. Ministry of Health, Labour and Welfare of Japan

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Mutations in the superoxide dismutase 1 (sod1) gene cause familial amyotrophic lateral sclerosis (FALS), likely due to the toxic properties of misfolded mutant SOD1 protein. Here we demonstrated that, starting from the pre-onset stage of FALS, misfolded SOD1 species associates specifically with kinesin-associated protein 3 (KAP3) in the ventral white matter of SOD1(G93A)-transgenic mouse spinal cord. KAP3 is a kinesin-2 subunit responsible for binding to cargos including choline acetyltransferase (ChAT). Motor axons in SOD1(G93A)-Tg mice also showed a reduction in ChAT transport from the pre-onset stage. By employing a novel FALS modeling system using NG108-15 cells, we showed that microtubule-dependent release of acetylcholine was significantly impaired by misfolded SOD1 species. Furthermore, such impairment was able to be normalized by KAP3 overexpression. KAP3 was incorporated into SOD1 aggregates in human FALS cases as well. These results suggest that KAP3 sequestration by misfolded SOD1 species and the resultant inhibition of ChAT transport play a role in the dysfunction of ALS.

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