5-Hydroxytryptamine 4(a) Receptor Is Coupled to the Gα Subunit of Heterotrimeric G13 Protein
Serotonin (5-hydroxytryptamine (5-HT)) is an important neurotransmitter that regulates multiple events in the central nervous system. Many of the 5-HT functions are mediated via G protein-coupled receptors that are coupled to multiple heterotrimeric G proteins, including Gs, Gi, and Gq subfamilies (...
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Published in | The Journal of biological chemistry Vol. 277; no. 23; pp. 20812 - 20819 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
07.06.2002
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Online Access | Get full text |
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Summary: | Serotonin (5-hydroxytryptamine (5-HT)) is an important neurotransmitter that regulates multiple events in the central nervous system. Many of the 5-HT functions are mediated via G protein-coupled receptors that are coupled to multiple heterotrimeric G proteins, including Gs, Gi, and Gq subfamilies (Martin, G. R., Eglen, R. M., Hamblin, M. W., Hoyer, D., and Yocca, F. (1998)Trends Pharmacol. Sci. 19, 2–4). Here we show for the first time that the 5-hydroxytryptamine 4(a) receptor (5-HT4(a)) is coupled not only to heterotrimeric Gs but also to G13 protein, as assessed both by biochemical and functional assays. Using reconstitution of 5-HT4(a) receptor with different G proteins in Spodoptera frugiperda (Sf.9) cells, we have proved that agonist stimulation of receptor-induced guanosine 5′-(3-O-thio)triphosphate binding to Gα13protein. We then determined that expression of 5-HT4(a)receptor in mammalian cells induced constitutive- as well as agonist-promoted activation of a transcription factor, serum response element, through the activation of Gα13 and RhoA. Finally, we have determined that expression of 5-HT4(a)receptor in neuroblastoma × glioma NIE-115 cells cause RhoA-dependent neurite retraction and cell rounding under basal conditions and after agonist stimulation. These data suggest that by activating 5-HT4(a) receptor-G13 pathway, serotonin plays a prominent role in regulating neuronal architecture in addition to its classical role in neurotransmission. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M112216200 |