Literature DB >> 30833707

Ligand-induced activation of ERK1/2 signaling by constitutively active Gs-coupled 5-HT receptors.

Ping Liu1,2, Yu-Ling Yin1,2, Ting Wang1,2,3, Li Hou1, Xiao-Xi Wang1, Man Wang1, Guan-Guan Zhao1, Yi Shi1, H Eric Xu4,5,6,7, Yi Jiang8,9.   

Abstract

5-HT4R, 5-HT6R, and 5-HT7AR are three constitutively active Gs-coupled 5-HT receptors that have key roles in brain development, learning, memory, cognition, and other physiological processes in the central nervous system. In addition to Gs signaling cascade mediated by these three 5-HT receptors, the ERK1/2 signaling which is dependent on cyclic adenosine monophosphate (cAMP) production and protein kinase A (PKA) activation downstream of Gs signaling has also been widely studied. In this study, we investigated these two signaling pathways originating from the three Gs-coupled 5-HT receptors in AD293 cells. We found that the phosphorylation and activation of ERK1/2 are ligand-induced, in contrast to the constitutively active Gs signaling. This indicates that Gs signaling alone is not sufficient for ERK1/2 activation in these three 5-HT receptors. In addition to Gs, we found that β-arrestin and Fyn are essential for the activation of ERK1/2. Together, these results put forth a novel mechanism for ERK1/2 activation involving the cooperative action of Gs, β-arrestin, and Fyn.

Entities:  

Keywords:  5-HT; 5-HT4R; 5-HT6R; 5-HT7AR; ERK1/2; Fyn; Gs; Src; β-arrestin

Mesh:

Substances:

Year:  2019        PMID: 30833707      PMCID: PMC6786432          DOI: 10.1038/s41401-018-0204-6

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


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