Premium
Altered levels and distribution of microtubule‐associated proteins before disease onset in a mouse model of amyotrophic lateral sclerosis
Author(s) -
Farah C. Abi,
Nguyen M. D.,
Julien J. P.,
Leclerc N.
Publication year - 2003
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2003.01505.x
Subject(s) - amyotrophic lateral sclerosis , sod1 , neurodegeneration , microtubule , microtubule associated protein , biology , axoplasmic transport , tau protein , gene isoform , spinal cord , cytoskeleton , microbiology and biotechnology , kinesin , alzheimer's disease , neuroscience , pathology , biochemistry , disease , medicine , gene , cell
Alterations of the axonal transport and microtubule network are potential causes of motor neurodegeneration in mice expressing a mutant form of the superoxide dismutase 1 (SOD1 G37R ) linked to amyotrophic lateral sclerosis (ALS). In the present study, we investigated the biology of microtubule‐associated proteins (MAPs), responsible for the formation and stabilization of microtubules, in SOD1 G37R mice. Our results show that the protein levels of MAP2, MAP1A, tau 100 kDa and tau 68 kDa species decrease significantly as early as 5 months before onset of symptoms in the spinal cord of SOD1 G37R mice, whereas decrease in levels of tau 52–55 kDa species is most often noted with the manifestation of the clinical symptoms. Interestingly, there was no change in the protein levels of MAPs in the brain of SOD1 G37R mice, a CNS organ spared by the mutant SOD1 toxicity. Remarkably, as early as 5 months before disease onset, the binding affinities of MAP1A, MAP2 and tau isoforms to the cytoskeleton decreased in spinal cord of SOD1 G37R mice. This change correlated with a hyperphosphorylation of the soluble tau 52–55 kDa species at epitopes recognized by the antibodies AT8 and PHF‐1. Finally, a shift in the distribution of MAP2 from the cytosol to the membrane is detected in SOD1 G37R mice at the same stage. Thus, alterations in the integrity of microtubules are early events of the neurodegenerative processes in SOD1 G37R mice.