Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate
Identifieur interne : 001024 ( Ncbi/Checkpoint ); précédent : 001023; suivant : 001025Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate
Auteurs : Marie-Hélène Canron [France] ; Martine Perret [France] ; Anne Vital [France] ; Erwan Bézard [France] ; Benjamin Dehay [France]Source :
- Scientific Reports [ 2045-2322 ] ; 2012.
English descriptors
- KwdEn :
- Aging (metabolism), Aging (pathology), Alzheimer Disease (metabolism), Alzheimer Disease (pathology), Amyloid beta-Peptides (chemistry), Amyloid beta-Peptides (metabolism), Animals, Brain (metabolism), Brain (pathology), Brain Mapping, Cheirogaleidae, Disease Models, Animal, Female, Immunohistochemistry, Male, Parkinson Disease (metabolism), Parkinson Disease (pathology), Phosphorylation, Protein Folding, alpha-Synuclein (chemistry), alpha-Synuclein (metabolism).
- MESH :
- chemical , chemistry : Amyloid beta-Peptides, alpha-Synuclein.
- metabolism : Aging, Alzheimer Disease, Amyloid beta-Peptides, Brain, Parkinson Disease, alpha-Synuclein.
- pathology : Aging, Alzheimer Disease, Brain, Parkinson Disease.
- Animals, Brain Mapping, Cheirogaleidae, Disease Models, Animal, Female, Immunohistochemistry, Male, Phosphorylation, Protein Folding.
Abstract
Since age-dependent deposition of Aβ-amyloid has been reported in the
Url:
DOI: 10.1038/srep00910
PubMed: 23205271
PubMed Central: 3510464
Affiliations:
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Links to Exploration step
PMC:3510464Le document en format XML
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<series><title level="j">Scientific Reports</title>
<idno type="eISSN">2045-2322</idno>
<imprint><date when="2012">2012</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aging (metabolism)</term>
<term>Aging (pathology)</term>
<term>Alzheimer Disease (metabolism)</term>
<term>Alzheimer Disease (pathology)</term>
<term>Amyloid beta-Peptides (chemistry)</term>
<term>Amyloid beta-Peptides (metabolism)</term>
<term>Animals</term>
<term>Brain (metabolism)</term>
<term>Brain (pathology)</term>
<term>Brain Mapping</term>
<term>Cheirogaleidae</term>
<term>Disease Models, Animal</term>
<term>Female</term>
<term>Immunohistochemistry</term>
<term>Male</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (pathology)</term>
<term>Phosphorylation</term>
<term>Protein Folding</term>
<term>alpha-Synuclein (chemistry)</term>
<term>alpha-Synuclein (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Amyloid beta-Peptides</term>
<term>alpha-Synuclein</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Aging</term>
<term>Alzheimer Disease</term>
<term>Amyloid beta-Peptides</term>
<term>Brain</term>
<term>Parkinson Disease</term>
<term>alpha-Synuclein</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Aging</term>
<term>Alzheimer Disease</term>
<term>Brain</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Brain Mapping</term>
<term>Cheirogaleidae</term>
<term>Disease Models, Animal</term>
<term>Female</term>
<term>Immunohistochemistry</term>
<term>Male</term>
<term>Phosphorylation</term>
<term>Protein Folding</term>
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<front><div type="abstract" xml:lang="en"><p>Since age-dependent deposition of Aβ-amyloid has been reported in the <italic>Microcebus</italic>
<italic>murinus</italic>
, we posited that this animal could as well be a model of age-related synucleinopathy. We characterized the distribution of Aβ-amyloid, α-synuclein and two of its modified forms in the brain of <italic>Microcebus</italic>
<italic>murinus</italic>
aged from 1.5 to 10 years. Intracytoplasmic α-synuclein aggregates were observed only in aged animals in different brain regions, which were also phospho-Ser129 and nitrated α-synuclein immunoreactive. Age-dependent α-synuclein aggregation occurs spontaneously in mouse lemur primates. <italic>Microcebus murinus</italic>
may provide a model to study age-associated α-synucleinopathy and for testing putative therapeutic interventions for both Alzheimer's and Parkinson's diseases.</p>
</div>
</front>
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