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PLoS One ; 9(1): e86617, 2014.
Article in English | MEDLINE | ID: mdl-24466171

ABSTRACT

CCAAT-enhancer binding proteins are transcription factors that help to regulate a wide range of inflammatory mediators, as well as several key elements of energy metabolism. Because C/EBPs are expressed by rodent astrocytes and microglia, and because they are induced by pro-inflammatory cytokines that are chronically upregulated in the Alzheimer's disease (AD) cortex, we have investigated whether C/EBPs are expressed and upregulated in the AD cortex. Here, we demonstrate for the first time that C/EBPß can be detected by Western blots in AD and nondemented elderly (ND) cortex, and that it is significantly increased in AD cortical samples. In situ, C/EBPß localizes immunohistochemically to microglia. In microglia cultured from rapid autopsies of elderly patient's brains and in the BV-2 murine microglia cell line, we have shown that C/EBPß can be upregulated by C/EBP-inducing cytokines or lipopolysaccharide and exhibits nuclear translocation possibly indicating functional activity. Given the known co-regulatory role of C/EBPs in pivotal inflammatory mechanisms, many of which are present in AD, we propose that upregulation of C/EBPs in the AD brain could be an important orchestrator of pathogenic changes.


Subject(s)
Alzheimer Disease/metabolism , CCAAT-Enhancer-Binding Protein-beta/metabolism , Microglia/metabolism , Alzheimer Disease/genetics , Amyloid beta-Peptides/metabolism , Animals , Autopsy , Brain/metabolism , Brain/pathology , CCAAT-Enhancer-Binding Protein-beta/genetics , Cell Line , Cell Nucleus , Cells, Cultured , Frontal Lobe/metabolism , Frontal Lobe/pathology , Gene Expression , Humans , Immunohistochemistry , Mice , Protein Binding , Protein Transport
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