4.5 Article

Social interaction modulates the neuroinflammatory response to global cerebral ischemia in male mice

期刊

BRAIN RESEARCH
卷 1673, 期 -, 页码 86-94

出版社

ELSEVIER
DOI: 10.1016/j.brainres.2017.08.008

关键词

Social isolation; Global cerebral ischemia; Neuroinflammation

资金

  1. National Institute of Mental Health [MH107002]
  2. National Institute of Neurological Disorders and Stroke [NS092388]

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Social isolation is a risk factor for cardiovascular and cerebrovascular diseases, although the underlying mechanisms remain underspecified. Considering the potential of microglia to become sensitized by stressors and their role in neuroinflammation, we hypothesized that social isolation primes microglia, resulting in an exaggerated neuroimmune response to experimental cerebral ischemia. First, major histocompatibility complex II (MHC II) gene expression, an indicator of microglial priming, was compared between mice that were socially isolated or pair-housed. MHC II increased in the hippocampus and cortex of socially isolated mice, which is suggestive of isolation-induced microglial priming. In experiment 2, isolated and pair-housed mice underwent similar to 8 min of global cerebral ischemia. Hippocampal mRNA expression of tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) was significantly increased among both isolated and pair-housed ischemia groups relative to sham controls. Hippocampal expression of interleukin 1 beta (IL-1 beta and cortical INF-alpha, IL-1 beta and IL-6, were significantly increased 24-h postischemia in isolated mice, but not pair-housed mice, relative to controls. Ischemia-induced increases in microglial cell body area and percent area fraction of ionized calcium binding adaptor molecule 1 (Iba-1) positive staining were also observed in isolated, but not pair-housed mice, relative to controls. For experiment 3, brain sections from socially isolated and pair-housed mice underwent 15 min of oxygen glucose deprivation (OGD), an ex vivo model of cerebral ischemia. IL-6 gene expression was significantly elevated following OGD only in hippocampi from mice that had been socially isolated, indicating that isolation prior to ischemia is sufficient to modulate the neuroinflammatory response. Together, these data suggest microglial priming as a possible mechanism underlying the detrimental effects of social isolation on cerebral ischemia outcome. (C) 2017 Elsevier B.V. All rights reserved.

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