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Brain-resident microglia predominate over infiltrating myeloid cells in activation, phagocytosis and interaction with T-lymphocytes in the MPTP mouse model of Parkinson disease
被引:93
作者:
Depboylu, Candan
[1
,2
]
Stricker, Sarah
[3
,4
]
Ghobril, Jean-Pierre
[1
,2
]
Oertel, Wolfgang H.
[1
,2
]
Priller, Josef
[3
,4
]
Hoeglinger, Guenter U.
[1
,2
,5
,6
]
机构:
[1] Univ Marburg, Dept Neurol, D-35043 Marburg, Germany
[2] Univ Marburg, Lab Expt Neurol, D-35043 Marburg, Germany
[3] Charite, Dept Neuropsychiat, D-13353 Berlin, Germany
[4] Charite, Lab Mol Psychiat, D-13353 Berlin, Germany
[5] Tech Univ Munich, Dept Neurol, Munich, Germany
[6] German Ctr Neurodegenerat Dis, Munich, Germany
关键词:
Microglia;
Phagocyte;
Lymphocyte;
Antigen presentation;
MPTP;
Parkinson disease;
CENTRAL-NERVOUS-SYSTEM;
FOCAL CEREBRAL-ISCHEMIA;
MARROW CHIMERIC MICE;
SUBSTANTIA-NIGRA;
DOPAMINERGIC-NEURONS;
GLIAL-CELLS;
HEMATOGENOUS MACROPHAGES;
REACTIVE MICROGLIA;
HUMAN NEUROMELANIN;
IN-VIVO;
D O I:
10.1016/j.expneurol.2012.08.020
中图分类号:
Q189 [神经科学];
学科分类号:
071006 [神经生物学];
摘要:
Parkinson disease (PD) is characterized by dopaminergic neurodegeneration in the substantia nigra (SN). Recent evidence suggests that innate and adaptive immune responses can influence dopaminergic cell death in animal models of PD. However, the precise role of mononuclear phagocytes, key players in damaged tissue clearance and cross-talk with cells of adaptive immune system, remains open in PD. Mononuclear phagocytes in the brain occur as brain-resident microglia and as brain-infiltrating myeloid cells. To elucidate their differential contribution in the uptake of dopaminergic cell debris and antigen presentation capacity, we labeled nigral dopaminergic neurons retrogradely with inert rhodamine-conjugated latex retrobeads before inducing their degeneration by subchronic 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) administration. We used green fluorescent protein (GFP)-expressing bone marrow chimeric mice to differentiate brain-infiltrating from brain-resident myeloid cells. We found that half of both endogenous (GFP-) and exogenous (GFP+) microglia (Iba1+) in the SN incorporated the tracer from degenerating dopaminergic neurons Id after MPTP intoxication. In absolute numbers, endogenous microglia were much more activated to macrophages compared to exogenous myeloid cells at Id after MPTP. Mainly the endogenous, tracer-phagocytosing microglia expressed the major histocompatibility complex (MHC) class II molecule for antigen presentation. Additionally, T-lymphocytes (Iba1-/GFP+/CD3+), which infiltrate the MPTP-lesioned SN, were mainly in direct contact with MHCII + endogenous microglia. Our data suggest that brain-resident microglia are predominantly implicated in the removal of dopaminergic cell debris and the cross-talk with infiltrating T-lymphocytes in the SN in the MPTP mouse model of PD. (C) 2012 Elsevier Inc. All rights reserved.
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页码:183 / 191
页数:9
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