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Brain Res ; 1026(2): 302-6, 2004 Nov 12.
Article in English | MEDLINE | ID: mdl-15488493

ABSTRACT

We investigated the role of the p38 mitogen-activated protein kinase (MAPK) pathway in heat-shock-induced neurite outgrowth of PC12 mutant cells in which nerve growth factor (NGF)-induced neurite outgrowth is impaired. When cultures of the PC12 mutant (PC12m3) cells were exposed to heat stress at 44 degrees C for 10 min, activity of p38 MAPK increased and neurite outgrowth was greatly enhanced. The neurite extension was inhibited by the p38 MAPK inhibitor BS203580. Longer heat treatment of PC12m3 cells provoked cell death, which was enhanced by SB203580. These findings suggest that heat-induced activation of p38 MAPK is responsible for the neurite outgrowth and survival of PC12m3 cells.


Subject(s)
Hot Temperature , Neurites/radiation effects , Shock , p38 Mitogen-Activated Protein Kinases/metabolism , Animals , Blotting, Western/methods , Cell Survival/drug effects , Enzyme Inhibitors/pharmacology , Imidazoles/pharmacology , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3/metabolism , Nerve Growth Factor/pharmacology , Neurites/drug effects , Neurites/physiology , PC12 Cells , Pyridines/pharmacology , Rats , Time Factors
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