Analysis of the Impact of CD200 on Phagocytosis
Autor: | Anthony Lyons, Janis Noonan, Veronica A. Campbell, Orla Fitzpatrick, Aedín M. Minogue, Marina A. Lynch, Raasay S. Jones |
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Rok vydání: | 2016 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty Neurology Phagocytosis Increased Phagocytosis Neuroscience (miscellaneous) Biology Hippocampus Interferon-gamma 03 medical and health sciences Cellular and Molecular Neuroscience 0302 clinical medicine Antigens CD Lysosome medicine Animals Rats Wistar Receptor PI3K/AKT/mTOR pathway Amyloid beta-Peptides Microglia Macrophage Activation Toll-Like Receptor 2 Cell biology 030104 developmental biology medicine.anatomical_structure Immunology Lysosomes 030217 neurology & neurosurgery Function (biology) |
Zdroj: | Molecular Neurobiology. 54:5730-5739 |
ISSN: | 1559-1182 0893-7648 |
DOI: | 10.1007/s12035-016-0223-6 |
Popis: | One factor that impacts on microglial activation is the interaction between the ubiquitously expressed CD200 and CD200R, which is expressed only on microglia in the brain. Decreased signalling through CD200R, when CD200 expression is reduced, results in microglial activation and may, at least in part, explain the increased cell activity that is observed with age, in models of Alzheimer's and Parkinson's disease as well as in the human diseases. There is evidence of increased microglial activation in CD200-deficient mice, and isolated microglia prepared from these mice are more reactive to inflammatory stimuli like Toll-like receptor 2 and 4 agonists, and interferon-γ. Here, we examined the impact of CD200 deficiency on amyloid-β (Aβ)-induced changes in microglia and report, perhaps unexpectedly, that the effect of Aβ was attenuated in microglia prepared from CD200-deficient mice. The evidence indicates that this is a consequence of increased phagocytosis, associated with increased lysosomal activity in CD200-deficient microglia. The data suggest that mTOR-related signalling is decreased in these cells and that inhibiting mTOR by rapamycin increases phagocytosis. Thus, while the findings to date have emphasized the anti-inflammatory effects of CD200-CD200R interaction, the present evidence indicates a previously unreported impact on lysosomal function. |
Databáze: | OpenAIRE |
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