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Neurobiol Dis. 2013 Aug;56:34-46. doi: 10.1016/j.nbd.2013.03.009. Epub 2013 Mar 28.

Calpains mediate axonal cytoskeleton disintegration during Wallerian degeneration.

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  • 1Department of Emergency Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. marekma@mail.med.upenn.edu

Abstract

In both the central nervous system (CNS) and peripheral nervous system (PNS), transected axons undergo Wallerian degeneration. Even though Augustus Waller first described this process after transection of axons in 1850, the molecular mechanisms may be shared, at least in part, by many human diseases. Early pathology includes failure of synaptic transmission, target denervation, and granular disintegration of the axonal cytoskeleton (GDC). The Ca(2+)-dependent protease calpains have been implicated in GDC but causality has not been established. To test the hypothesis that calpains play a causal role in axonal and synaptic degeneration in vivo, we studied transgenic mice that express human calpastatin (hCAST), the endogenous calpain inhibitor, in optic and sciatic nerve axons. Five days after optic nerve transection and 48 h after sciatic nerve transection, robust neurofilament proteolysis observed in wild-type controls was reduced in hCAST transgenic mice. Protection of the axonal cytoskeleton in sciatic nerves of hCAST mice was nearly complete 48 h post-transection. In addition, hCAST expression preserved the morphological integrity of neuromuscular junctions. However, compound muscle action potential amplitudes after nerve transection were similar in wild-type and hCAST mice. These results, in total, provide direct evidence that calpains are responsible for the morphological degeneration of the axon and synapse during Wallerian degeneration.

Copyright © 2013 Elsevier Inc. All rights reserved.

PMID:
23542511
[PubMed - indexed for MEDLINE]
PMCID:
PMC3721029
Free PMC Article

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