Papers

Peer-reviewed
Sep, 2015

Critical role of JSAP1 and JLP in axonal transport in the cerebellar Purkinje cells of mice

FEBS LETTERS
  • Tokiharu Sato
  • ,
  • Momoe Ishikawa
  • ,
  • Toru Yoshihara
  • ,
  • Ryota Nakazato
  • ,
  • Haruhiro Higashida
  • ,
  • Masahide Asano
  • ,
  • Katsuji Yoshioka

Volume
589
Number
19
First page
2805
Last page
2811
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.febslet.2015.08.024
Publisher
ELSEVIER SCIENCE BV

JNK/stress-activated protein kinase-associated protein 1 (JSAP1) and JNK-associated leucine zipper protein (JLP) are structurally related scaffolding proteins that are highly expressed in the brain. Here, we found that JSAP1 and JLP play functionally redundant and essential roles in mouse cerebellar Purldnje cell (PC) survival. Mice containing PCs with deletions in both JSAP1 and JLP exhibited PC axonal dystrophy, followed by gradual, progressive neuronal loss. Kinesin-1 cargoes accumulated selectively in the swollen axons of Jsap1/Jlp-deficient PCs. In addition, autophagy inactivation in these mice markedly accelerated PC degeneration. These findings suggest that JSAP1 and JLP play critical roles in kinesin-1-dependent axonal transport, which prevents brain neuronal degeneration. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Link information
DOI
https://doi.org/10.1016/j.febslet.2015.08.024
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26320416
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000362619700022&DestApp=WOS_CPL
ID information
  • DOI : 10.1016/j.febslet.2015.08.024
  • ISSN : 0014-5793
  • eISSN : 1873-3468
  • Pubmed ID : 26320416
  • Web of Science ID : WOS:000362619700022

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