Literature DB >> 22886465

Differential distribution and activation of microglia in the brain of male C57BL/6J mice.

Ting-Ting Yang1, Chingju Lin, Chao-Tien Hsu, Tzu-Feng Wang, Fang-Yi Ke, Yu-Min Kuo.   

Abstract

Upon certain stimuli, microglia undergo different degrees of transformation in order to maintain homeostasis of the CNS. However, chronic microglia activation has been suggested to play an active role in the pathogenesis of neurodegenerative diseases. The density of microglia and the degree of microglia activation vary among brain regions; such differences may underlie the brain region-specific characteristics of neurodegenerative diseases. In this study, we aim to characterize the temporal and spatial profiles of microglia activation induced by peripheral inflammation in male C57BL/6J mice. Our results showed that, on average, microglia densities were highest in the cortex, followed by the limbic area, basal nuclei, diencephalon, brainstem and cerebellum. Among the 22 examined brain nuclei/regions, the substantia nigra had the highest microglia density. Microglia morphological changes were evident within 3 h after a single intraperitoneal lipopolysaccharides injection, with the highest degree of changes also in the substantia nigra. The lipopolysaccharide-induced microglia activation, determined by maximal cell size, was positively correlated with density of microglia and levels of TNFα receptor 1; it was not correlated with original microglia cell size or integrity of blood-brain barrier. The differential response of microglia also cannot be explained by different types of neurotransmitters. Our works suggest that the high density of microglia and the high levels of TNFα receptor 1 in the substantia nigra make this brain region the most susceptible area to systemic immunological insults.

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Year:  2012        PMID: 22886465     DOI: 10.1007/s00429-012-0446-x

Source DB:  PubMed          Journal:  Brain Struct Funct        ISSN: 1863-2653            Impact factor:   3.270


  32 in total

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Review 2.  From development to dysfunction: microglia and the complement cascade in CNS homeostasis.

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4.  Loss of Brain Norepinephrine Elicits Neuroinflammation-Mediated Oxidative Injury and Selective Caudo-Rostral Neurodegeneration.

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5.  Local Cues Establish and Maintain Region-Specific Phenotypes of Basal Ganglia Microglia.

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Review 6.  Neuroinflammation in the normal aging hippocampus.

Authors:  R M Barrientos; M M Kitt; L R Watkins; S F Maier
Journal:  Neuroscience       Date:  2015-03-12       Impact factor: 3.590

7.  Co-Culture of Neurons and Microglia.

Authors:  Pamela J Roqué; Lucio G Costa
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8.  Substance P enhances microglial density in the substantia nigra through neurokinin-1 receptor/NADPH oxidase-mediated chemotaxis in mice.

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Journal:  Clin Sci (Lond)       Date:  2015-06-22       Impact factor: 6.124

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Journal:  Neurotoxicology       Date:  2016-08-16       Impact factor: 4.294

Review 10.  Neuroinflammatory challenges compromise neuronal function in the aging brain: Postoperative cognitive delirium and Alzheimer's disease.

Authors:  Giuseppe P Cortese; Corinna Burger
Journal:  Behav Brain Res       Date:  2016-08-17       Impact factor: 3.332

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