Journal
NEUROSCIENCE
Volume 187, Issue -, Pages 93-102Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2011.04.048
Keywords
NF-kappa B; phosphorylation; status epilepticus; neuronal damage; neuronal survival
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Funding
- National Research Foundation of Korea [2009-0064347, 2010K000808, 2009-0093812]
- National Research Foundation of Korea [2009-0064347] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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Although nuclear factor-kappa B (NF-kappa B) is essential for neuron survival and its activation may protect neuron against oxidative-stresses or ischemia-induced neurodegeneration, NF-kappa B activation can contribute to inflammatory reaction and apoptotic cell death after brain injury and stroke. However, there are little data concerning the specific pattern of NF-kappa B phosphorylations in neuronal damage/survival induced by status epilepticus (SE). In the present study, NF-kappa B phosphorylation showed the cellular specific pattern in responses to SE. p52-S865, p52-Ser869, p65-Ser276, p65-Ser311, p65-Ser468, and p65-Ser529 NF-kappa B phosphorylation was significantly decreased in the CA1 and CA3 pyramidal cells vulnerable to SE, although neuronal specific nuclear antigen immunoreactivity was strongly detected. In contrast, p65-Ser536 NF-kappa B phosphorylation was enhanced in these neurons accompanied by TUNEL- and Fluoro-Jade B 244signals. These findings serve as the first comprehensive description of the cellular specific distribution of NF-kappa B phosphorylation in response to pilocarpine-induced SE in the rat hippocampus, and suggest that enhancement in p65-Ser536 NF-kappa B phosphorylation may be closely relevant to neuronal vulnerability to SE, while others may be involved in neuronal survival. (C) 2011 Published by Elsevier Ltd on behalf of IBRO.
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