Glucocorticoid adrenal steroids and glucocorticoid-inducible kinase isoforms in the regulation of GluR6 expression

• Published in: The Journal of physiology 2005-06, Vol.565 (2), p.391-401
• Main Authors: Strutz‐Seebohm, Nathalie, Seebohm, Guiscard, Shumilina, Ekaterina, Mack, Andreas F., Wagner, Hans‐Joachim, Lampert, Angelika, Grahammer, Florian, Henke, Guido, Just, Lothar, Skutella, Thomas, Hollmann, Michael, Lang, Florian
• Format: Article
• Language: English
• Subjects: Animals; Cells, Cultured; Dexamethasone - pharmacology; Female; Gene Expression Regulation, Developmental - drug effects; Gene Expression Regulation, Developmental - physiology; Glucocorticoids - pharmacology; GluK2 Kainate Receptor; Hippocampus - cytology; Hippocampus - embryology; Immediate-Early Proteins; Isoenzymes - metabolism; Male; Mice; Mice, Inbred C57BL; Molecular and Genomic Physiology; Neurons - cytology; Neurons - physiology; Nuclear Proteins - metabolism; Oocytes; Patch-Clamp Techniques; Pregnancy; Protein Serine-Threonine Kinases - metabolism; Receptors, Kainic Acid - genetics; Receptors, Kainic Acid - metabolism; Up-Regulation - drug effects; Up-Regulation - physiology; Xenopus laevis
• ISSN: 0022-3751; 1469-7793
• DOI: 10.1113/jphysiol.2004.079624

Generation of memory is enhanced during stress, an effect attributed to stimulation of neuronal learning by adrenal glucocorticoids. The glucocorticoid-dependent genes include the serum- and glucocorticoid-inducible kinase SGK1. SGK1 is activated through the phosphatidylinositol 3 kinase (PI3-kinase) pathway by growth factors such as insulin-like growth factor-1 (IGF1) or tumour growth factor β (TGF-β). Previously, a fourfold higher expression of SGK1 has been observed in fast-learning rats as compared with slow-learning rats. The mechanisms linking glucocorticoids or SGK1 with neuronal function have, however, remained elusive. We show here that treatment of mice with the glucocorticoid dexamethasone (238 μg day −1 for 8–20 days) enhances hippocampal expression of GluR6. Immunohistochemistry reveals significantly enhanced GluR6 protein abundance at neurones but not at astrocytes in mice. Immunohistochemistry and patch clamp on hippocampal neurones in primary culture reveal upregulation of GluR6 protein abundance and kainate-induced currents following treatment with dexamethasone (1 μ m ) and TGF-β (1 μ m ). In Xenopus oocytes expressing rat GluR6, coexpression of SGK1 strongly increases glutamate-induced current at least partially by increasing the abundance of GluR6 protein in the plasma membrane. The related kinases SGK2 and SGK3 similarly stimulate GluR6, but are less effective than SGK1. The observations point to a novel mechanism regulating GluR6 which contributes to the regulation of neuronal function by glucocorticoids.