Calpain-mediated cleavage of collapsin response mediator protein(CRMP)-2 during neurite degeneration in mice

Ekatherina Touma, Satoko Kato, Koji Fukui, Tatsuro Koike

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

Axon or dendrite degeneration involves activation of the ubiquitin-proteasome system, failure to maintain neuritic ATP levels, microtubule fragmentation and a mitochondrial permeability transition that occur independently of the somal death programs. To gain further insight into the neurite degeneration mechanims we have compared two-dimensional gel electrophoresis patterns of neurite proteins from suprior cervical ganglia during degeneration caused by nerve growth factor (NGF) deprivation. We show here that collapsin response mediator protein (CRMP)-2 and CMRP-4 protein patterns were altered during beading formation, an early hallmark of neurite degeneration, prior to neurite fragmentation, the final stage of degeneration. Western blotting using a monoclonal antibody against CRMP-2 shows that the native form (64 kDa) was cleaved to generate a truncated form (58 kDa). No cleavage of CRMP-2 or -4 occurred in NGF-deprived neurites from Wlds (Wallerian degeneration slow) mutant mice in which neurite degeneration is markedly delayed. Using different protease inhibitors, purified calpain 1 protein and calpain 1-specific siRNA, we have demonstrated that CRMP-2 is a substrate for calpain 1. Indeed, caplain activity was activated at an early phase of neuronal degeneration in cerebellar granule neurons, and down-regulation of caplain 1 expression suppressed CRMP-2 cleavage. Furthermore, this cleavage occurred after vinblastine treatment or in vitro Wallerian degeneration, suggesting that it represents a common step in the process of dying neurites. CRMP-2 and -4 play a pivotal role in axonal growth and transport, and the C-terminus region of CRMP-2 is essential for its binding to kinesin-1. Hence, this cleavage will render them dysfunctional and subject to autophagic processing associated with beading formation, as evidenced by the finding that the truncated form was localized in the beadings.

Original languageEnglish
Pages (from-to)3368-3381
Number of pages14
JournalEuropean Journal of Neuroscience
Volume26
Issue number12
DOIs
Publication statusPublished - 2007 Dec
Externally publishedYes

Keywords

  • Axon
  • Beading
  • Calpain
  • NGF
  • Proteomics
  • Sympathetic ganglia

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Calpain-mediated cleavage of collapsin response mediator protein(CRMP)-2 during neurite degeneration in mice. / Touma, Ekatherina; Kato, Satoko; Fukui, Koji; Koike, Tatsuro.

In: European Journal of Neuroscience, Vol. 26, No. 12, 12.2007, p. 3368-3381.

Research output: Contribution to journalArticle

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