共 55 条
Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia
被引:95
作者:

Bae, Keun-Ryung
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机构:
DGIST, Dept Brain Sci, Taegu, South Korea DGIST, Dept Brain Sci, Taegu, South Korea

Shim, Hyun-Jung
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h-index: 0
机构:
DGIST, Dept Brain Sci, Taegu, South Korea DGIST, Dept Brain Sci, Taegu, South Korea

Balu, Deebika
论文数: 0 引用数: 0
h-index: 0
机构:
Michigan State Univ, Dept Neurol & Ophthalmol, E Lansing, MI 48824 USA DGIST, Dept Brain Sci, Taegu, South Korea

Kim, Sang Ryong
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机构:
DGIST, Dept Brain Sci, Taegu, South Korea DGIST, Dept Brain Sci, Taegu, South Korea

Yu, Seong-Woon
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h-index: 0
机构:
DGIST, Dept Brain Sci, Taegu, South Korea DGIST, Dept Brain Sci, Taegu, South Korea
机构:
[1] DGIST, Dept Brain Sci, Taegu, South Korea
[2] Michigan State Univ, Dept Neurol & Ophthalmol, E Lansing, MI 48824 USA
关键词:
Translocator protein 18 kDa;
Microglia;
Neuroinflammation;
NF-kappa B;
Neurodegeneration;
PERIPHERAL BENZODIAZEPINE-RECEPTOR;
IN-VIVO;
MACROPHAGE ACTIVATION;
DOPAMINERGIC-NEURONS;
PARKINSONS-DISEASE;
MULTIPLE-SCLEROSIS;
NEUROTOXICITY;
EXPRESSION;
LIGANDS;
BINDING;
D O I:
10.1007/s11481-014-9540-6
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Translocator protein 18 kDa (TSPO) is a mitochondrial outer membrane protein. Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that TSPO is a negative regulator of neuroinflammation in microglia. Over-expression of TSPO decreased production of pro-inflammatory cytokines upon lipopolysaccharide treatment while TSPO knock-down had the opposite effect. Anti-inflammatory activity of TSPO is also supported by increased expression of alternatively activated M2 stage-related genes. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism. We also provide the evidence that the repressive activity of TSPO is at least partially mediated by the attenuation of NF-kappa B activation. Neurodegenerative diseases are characterized by loss of specific subsets of neurons at the particular anatomical regions of the central nervous system. Cause of neuronal death is still largely unknown, but it is becoming clear that neuroinflammation plays a significant role in the pathophysiology of neurodegenerative diseases. Understanding the mechanisms underlying the inhibitory effects of TSPO on neuroinflammation can contribute to the therapeutic design for neurodegenerative diseases.
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页码:424 / 437
页数:14
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