Enhanced activation of Akt and extracellular‐regulated kinase pathways by simultaneous occupancy of Gq‐coupled 5‐HT2A receptors and Gs‐coupled 5‐HT7A receptors in PC12 cells

• Published in: Journal of neurochemistry 2005-01, Vol.92 (1), p.72-82
• Main Authors: Johnson‐Farley, Nadine N., Kertesy, Sylvia B., Dubyak, George R., Cowen, Daniel S.
• Format: Article
• Language: English
• Subjects: 5‐HT2A receptor; 5‐HT7 receptor; Akt; Amphetamines - pharmacology; Animals; Biological and medical sciences; Enzyme Activation - drug effects; Enzyme Activation - physiology; Extracellular Signal-Regulated MAP Kinases - metabolism; extracellular signal‐regulated kinase; GTP-Binding Protein alpha Subunits, Gq-G11 - metabolism; GTP-Binding Protein alpha Subunits, Gq-G11 - pharmacology; GTP-Binding Protein alpha Subunits, Gs - metabolism; GTP-Binding Protein alpha Subunits, Gs - physiology; MAP Kinase Signaling System - drug effects; MAP Kinase Signaling System - physiology; Medical sciences; Neuropharmacology; PC12; PC12 Cells; Pharmacology. Drug treatments; Protein-Serine-Threonine Kinases - metabolism; Proto-Oncogene Proteins - metabolism; Proto-Oncogene Proteins c-akt; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease); Psychology. Psychoanalysis. Psychiatry; Psychopharmacology; Rats; Receptor, Serotonin, 5-HT2A - metabolism; Receptor, Serotonin, 5-HT2A - physiology; Receptors, Serotonin - metabolism; Receptors, Serotonin - physiology; serotonin (5‐HT); Serotonin - pharmacology; Serotonin 5-HT2 Receptor Agonists
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/j.1471-4159.2004.02832.x

The most commonly prescribed antidepressants, the serotonin (5‐HT) selective reuptake inhibitors, increase 5‐HT without targeting specific receptors. Yet, little is known about the interaction of multiple receptor subtypes expressed by individual neurons. Specifically, the effect of increases in cAMP induced by Gs‐coupled 5‐HT receptor subtypes on the signaling pathways modulated by other receptor subtypes has not been studied. We have, therefore, examined the activation of the extracellular‐regulated kinase (ERK) and Akt pathways by Gs‐coupled 5‐HT7A receptors and Gq‐coupled 5‐HT2A receptors, which are co‐expressed in discrete brain regions. Agonists for both receptors were found to activate ERK and Akt in transfected PC12 cells. 5‐HT2A receptor‐mediated activation of the two pathways was found to be Ca2+‐dependent. In contrast, 5‐HT7A receptor‐mediated activation of Akt required increases in both [cAMP] and intracellular [Ca2+], while activation of ERK was inhibited by Ca2+. The activation of ERK and Akt stimulated by simultaneous treatment of cells with 5‐HT2A and 5‐HT7A receptor agonists was found to be at least additive. Cell‐permeable cAMP analogs mimicked 5‐HT7A receptor agonists in enhancing 5‐HT2A receptor‐mediated activation of ERK and Akt. A role was identified for the cAMP–guanine exchange factor, Epac, in this augmentation of ERK, but not Akt, activation. Our finding of enhanced activation of neuroprotective Akt and ERK pathways by simultaneous occupancy of 5‐HT2A and 5‐HT7A receptors may also be relevant to the interaction of other neuronally expressed Gq‐ and Gs‐coupled receptors.