Premium
Mapping and kinetics of microglia/neuron cell‐to‐cell contacts in the 6‐OHDA murine model of Parkinson's disease
Author(s) -
VirgoneCarlotta Angélique,
Uhlrich Josselin,
Akram Muhammad Numan,
Ressnikoff Denis,
Chrétien Fabrice,
Domenget Chantal,
Gherardi Romain,
Despars Geneviève,
Jurdic Pierre,
Honnorat Jérôme,
Nataf Serge,
Touret Monique
Publication year - 2013
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.22546
Subject(s) - microglia , neurodegeneration , biology , neuroscience , substantia nigra , neuroinflammation , neuron , parkinson's disease , neuroglia , cx3cr1 , microbiology and biotechnology , dopaminergic , immunology , pathology , inflammation , central nervous system , disease , medicine , dopamine , chemokine , chemokine receptor
As neuroinflammatory processes are involved in the pathogenesis of Parkinson's disease (PD), we provide several key data describing the time‐course of microglial accumulation in relation with behavioral alterations and neurodegeneration in a murine model of PD induced by intrastriatal injection of 6‐hydroxydopamine (6‐OHDA). Our study argues for a major role of microglia which accumulation is somehow early and transient in spite of the neuronal loss progression. Moreover, we observed less 6‐OHDA‐induced neurodegeneration associated with less inflammatory reaction in DAP‐12 Knock‐In mice. The direct cell‐to‐cell contacts that may support physical interactions between microglia and altered dopaminergic neurons are ill‐defined, while it is currently hypothesized that microglia support an immune‐mediated amplification of neurodegeneration by establishing a molecular cross talk with neurons. Indeed, we sought to map microglia/neuron appositions in substantia nigra (SN) of 6‐OHDA injected C57Bl/6 mice and CX3CR1/ GFP/+ mice. Confocal immunofluorescence analyses followed by 3D reconstitutions reveal close appositions between the soma of TH+ neurons and microglial cell bodies and ramifications. Interestingly, some microglial ramifications penetrated TH + somas and about 40% of GFP + microglial cells in the injured SN harbored TH + intracytoplasmic inclusions. These results suggest a direct cross talk between neurons and microglia that may exert a microphagocytic activity toward TH+ neurons. Altogether, these results obtained in a murine PD model may participate in the understanding of microglial cells' function in neurodegenerative diseases. GLIA 2013;61:1645–1658