Region‐Specific Targets of p42/p44MAPK Signaling in Rat Brain

• Published in: Journal of neurochemistry 1998-02, Vol.70 (2), p.558-571
• Main Authors: Bhat, Ratan V., Engber, Thomas M., Finn, James P., Koury, Elizabeth J., Contreras, Patricia C., Miller, Matthew S., Dionne, Craig A., Walton, Kevin M.
• Format: Article
• Language: English
• Subjects: Anatomy; Animals; Biological and medical sciences; Brain - physiology; Calcium-Calmodulin-Dependent Protein Kinases - antagonists & inhibitors; Calcium-Calmodulin-Dependent Protein Kinases - metabolism; Cell Nucleus - physiology; Central nervous system; Cerebral Cortex - physiology; Cyclic AMP response element binding protein; Cytoplasm - metabolism; c‐Fos; Electroshock; Elk1; Enzyme Inhibitors - pharmacology; Erk2; Flavonoids - pharmacology; Fundamental and applied biological sciences. Psychology; Hippocampus; Hippocampus - physiology; MAP Kinase Kinase 1; Microtubule-Associated Proteins - metabolism; Microtubule‐associated protein 2; Mitogen-Activated Protein Kinase 1 - metabolism; Mitogen-Activated Protein Kinase 3; Mitogen-Activated Protein Kinase Kinases; Mitogen-Activated Protein Kinases; Mitogen‐activated protein kinase; Neuronal function; Organ Specificity; Phosphorylation; Protein-Serine-Threonine Kinases - metabolism; Protein-Tyrosine Kinases - metabolism; Proto-Oncogene Proteins c-fos - biosynthesis; Rats; Rats, Sprague-Dawley; Signal transduction; Signal Transduction - physiology; Vertebrates: nervous system and sense organs
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1046/j.1471-4159.1998.70020558.x

: In vitro studies indicate that p42/p44MAPK phosphorylate both nuclear and cytoplasmic proteins. However, the functional targets of p42/p44MAPK activation in vivo remain unclear. To address this question, we localized activated p42/p44MAPK in hippocampus and cortex and determined their signaling effects after electroconvulsive shock treatment (ECT) in rats. Phosphorylated p42/p44MAPK content increased in the cytoplasm of hippocampal neurons in response to ECT. Consistent with this cytoplasmic localization, inhibition of ECT‐induced p42/p44MAPK activation by the extracellular signal‐regulated kinase kinase inhibitor PD098059 blocked phosphorylation of the cytoplasmic protein microtubule‐associated protein 2c (MAP2c), but failed to inhibit the induction of the nuclear protein c‐Fos in response to ECT. In contrast to hippocampal neurons, cortical neurons exhibited an increase in amount of phosphorylated p42/p44MAPK in both the nucleus and cytoplasm after ECT. Accordingly, PD098059 blocked the induction of Fos‐like immunoreactivity in the nuclei of cortical neurons as well as MAP2c phosphorylation in the cytoplasm. Our data indicate that both nuclear and cytoplasmic substrates can be activated by p42/p44MAPK in vivo. However, the functional targets of p42/p44MAPK signaling depend on the precise location of p42/p44MAPK within different subcellular compartments of brain regions. These results indicate unique functional pathways of p42/p44MAPK‐mediated signal transduction within different brain regions in vivo.