Exercise reduces activation of microglia isolated from hippocampus and brain of aged mice

被引:106
作者
Kohman, Rachel A. [1 ,2 ]
Bhattacharya, Tushar K. [1 ]
Wojcik, Elzbieta [1 ]
Rhodes, Justin S. [1 ]
机构
[1] Univ Illinois, Beckman Inst, Dept Psychol, Urbana, IL 61801 USA
[2] Univ N Carolina, Dept Psychol, Wilmington, NC 28403 USA
关键词
Exercise; Hippocampus; Aging; Microglia; MHC II; CD86; CD206; LONG-TERM POTENTIATION; INNATE IMMUNE-SYSTEM; ADULT-MOUSE BRAIN; ALZHEIMERS-DISEASE; SICKNESS BEHAVIOR; EXPRESSION; NEUROGENESIS; REGIONS; INFLAMMATION; PHENOTYPE;
D O I
10.1186/1742-2094-10-114
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Aging is associated with low-grade neuroinflammation that includes basal increases in proinflammatory cytokines and expression of inflammatory markers on microglia. Exercise can reduce neuroinflammation following infection in aged animals, but whether exercise modulates basal changes in microglia activation is unknown. Therefore, we evaluated changes in basal microglia activation in cells isolated from the hippocampus and remaining brain following running-wheel access. Methods: Adult (4 months) and aged (22 months) male and female BALB/c mice were housed with or without running wheels for 10 weeks. Microglia were isolated from the hippocampus or remaining brain. Flow cytometry was used to determine microglia (CD11b+ and CD45(low)) that co-labeled with CD86, CD206, and MHC II. Results: Aged mice showed a greater proportion of CD86 and MHC II positive microglia. In aged females, access to a running wheel decreased proportion of CD86+ and MHC II+ microglia in the hippocampus whereas aged males in the running group showed a decrease in the proportion of CD86+ microglia in the brain and an increase in the proportion of MHC II+ microglia in hippocampus and brain. Conclusion: Overall, these data indicate that running-wheel access modulates microglia activation, but these effects vary by age, sex, and brain region.
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页数:9
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共 42 条
[31]   Efficient isolation of live microglia with preserved phenotypes from adult mouse brain [J].
Nikodemova, Maria ;
Watters, Jyoti J. .
JOURNAL OF NEUROINFLAMMATION, 2012, 9
[32]   Microglia Phenotype Diversity [J].
Olah, M. ;
Biber, K. ;
Vinet, J. ;
Boddeke, H. W. G. M. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2011, 10 (01) :108-118
[33]   ALTERED ANTIGEN EXPRESSION OF MICROGLIA IN THE AGED RODENT CNS [J].
PERRY, VH ;
MATYSZAK, MK ;
FEARN, S .
GLIA, 1993, 7 (01) :60-67
[34]   Differential expression of inflammatory mediators in rat microglia cultured from different brain regions [J].
Ren, LQ ;
Lubrich, B ;
Biber, K ;
Gebicke-Haerter, PJ .
MOLECULAR BRAIN RESEARCH, 1999, 65 (02) :198-205
[35]   Patterns of brain activity associated with variation in voluntary wheel-running behavior [J].
Rhodes, JS ;
Garland, T ;
Gammie, SC .
BEHAVIORAL NEUROSCIENCE, 2003, 117 (06) :1243-1256
[36]   Microglia derived from aging mice exhibit an altered inflammatory profile [J].
Sierra, Amanda ;
Gottfried-Blackmore, Andres C. ;
McEwen, Bruce S. ;
Bulloch, Karen .
GLIA, 2007, 55 (04) :412-424
[37]   The positive false discovery rate:: A Bayesian interpretation and the q-value [J].
Storey, JD .
ANNALS OF STATISTICS, 2003, 31 (06) :2013-2035
[38]   Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer's disease [J].
Streit, Wolfgang J. ;
Braak, Heiko ;
Xue, Qing-Shan ;
Bechmann, Ingo .
ACTA NEUROPATHOLOGICA, 2009, 118 (04) :475-485
[39]   Microglia: gatekeepers of central nervous system immunology [J].
Tambuyzer, Bart R. ;
Ponsaerts, Peter ;
Nouwen, Etienne J. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2009, 85 (03) :352-370
[40]   Chronic stress alters the density and morphology of microglia in a subset of stress-responsive brain regions [J].
Tynan, Ross J. ;
Naicker, Sundresan ;
Hinwood, Madeleine ;
Nalivaiko, Eugene ;
Buller, Kathryn M. ;
Pow, David V. ;
Day, Trevor A. ;
Walker, Frederick R. .
BRAIN BEHAVIOR AND IMMUNITY, 2010, 24 (07) :1058-1068