| Literature DB >> 10217284 |
K Hensley1, R A Floyd, N Y Zheng, R Nael, K A Robinson, X Nguyen, Q N Pye, C A Stewart, J Geddes, W R Markesbery, E Patel, G V Johnson, G Bing.
Abstract
The p38 mitogen-activated protein kinase is a stress-activated enzyme responsible for transducing inflammatory signals and initiating apoptosis. In the Alzheimer's disease (AD) brain, increased levels of phosphorylated (active) p38 were detected relative to age-matched normal brain. Intense phospho-p38 immunoreactivity was associated with neuritic plaques, neuropil threads, and neurofibrillary tangle-bearing neurons. The antibody against phosphorylated p38 recognized many of the same structures as an antibody against aberrantly phosphorylated, paired helical filament (PHF) tau, although PHF-positive tau did not cross-react with the phospho-p38 antibody. These findings suggest a neuroinflammatory mechanism in the AD brain, in which aberrant protein phosphorylation affects signal transduction elements, including the p38 kinase cascade, as well as cytoskeletal components.Entities:
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Year: 1999 PMID: 10217284 DOI: 10.1046/j.1471-4159.1999.0722053.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372