HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Early axonal loss accompanied by impaired endocytosis, abnormal axonal transport, and decreased microtubule stability occur in the model of Krabbe's disease.

Abstract
In Krabbe's disease (KD), a leukodystrophy caused by β-galactosylceramidase deficiency, demyelination and a myelin-independent axonopathy contributes to the severe neuropathology. Beyond axonopathy, we show that in Twitcher mice, a model of KD, a decreased number of axons both in the PNS and in the CNS, and of neurons in dorsal root ganglia (DRG), occurred before the onset of demyelination. Despite the early axonal loss, and although in vitro Twitcher neurites degenerated over time, Twitcher DRG neurons displayed an initial neurite overgrowth and, following sciatic nerve injury, Twitcher axons were regeneration-competent, at a time point where axonopathy was already ongoing. Psychosine, the toxic substrate that accumulates in KD, induced lipid raft clustering. At the mechanistic level, TrkA recruitment to lipid rafts was dysregulated in Twitcher neurons, and defective activation of the ERK1/2 and AKT pathways was identified. Besides defective recruitment of signaling molecules to lipid rafts, the early steps of endocytosis and the transport of endocytic and synaptic vesicles were impaired in Twitcher DRG neurons. Defects in axonal transport, specifically in the retrograde component, correlated with decreased levels of dynein, abnormal levels of post-translational tubulin modifications and decreased microtubule stability. The identification of the axonal defects that precede demyelination in KD, together with the finding that Twitcher axons are regeneration-competent when axonopathy is already installed, opens new windows of action to effectively correct the neuropathology that characterizes this disorder.
AuthorsCarla Andreia Teixeira, Catarina Oliveira Miranda, Vera Filipe Sousa, Telma Emanuela Santos, Ana Rita Malheiro, Melani Solomon, Gustavo H Maegawa, Pedro Brites, Mónica Mendes Sousa
JournalNeurobiology of disease (Neurobiol Dis) Vol. 66 Pg. 92-103 (Jun 2014) ISSN: 1095-953X [Electronic] United States
PMID24607884 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 Elsevier Inc. All rights reserved.
Chemical References
  • Tubulin
  • Dyneins
Topics
  • Animals
  • Axonal Transport (physiology)
  • Axons (pathology, physiology)
  • Cells, Cultured
  • Disease Models, Animal
  • Dyneins (metabolism)
  • Endocytosis (physiology)
  • Female
  • Ganglia, Spinal (pathology, physiopathology)
  • Leukodystrophy, Globoid Cell (pathology, physiopathology)
  • Male
  • Membrane Microdomains (pathology, physiology)
  • Mice
  • Mice, Neurologic Mutants
  • Microtubules (metabolism)
  • Motor Neurons (pathology, physiology)
  • Neurites (pathology, physiology)
  • Neurons (pathology, physiology)
  • Sciatic Nerve (injuries, pathology, physiopathology)
  • Synaptic Vesicles (pathology, physiology)
  • Transport Vesicles (pathology, physiology)
  • Tubulin (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: