Ligand-induced activation of ERK1/2 signaling by constitutively active G(s)-coupled 5-HT receptors
2019-09
发表期刊ACTA PHARMACOLOGICA SINICA
ISSN1671-4083
卷号40期号:9页码:1157-1167
发表状态已发表
DOI10.1038/s41401-018-0204-6
摘要

5-HT4R, 5-HT6R, and 5-HT7AR are three constitutively active G(s)-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 G(s) 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 G(s) signaling has also been widely studied. In this study, we investigated these two signaling pathways originating from the three G(s)-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 G(s) signaling. This indicates that G(s) signaling alone is not sufficient for ERK1/2 activation in these three 5-HT receptors. In addition to G(s), we found that beta-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 G(s), beta-arrestin, and Fyn.

关键词5-HT4R 5-HT6R 5-HT7AR 5-HT ERK1/2 G(s) beta-arrestin Fyn Src
收录类别SCI ; SCIE
资助项目Ministry of Science and Technology of China[XDB08020303]
WOS研究方向Chemistry ; Pharmacology & Pharmacy
WOS类目Chemistry, Multidisciplinary ; Pharmacology & Pharmacy
WOS记录号WOS:000484000100003
出版者NATURE PUBLISHING GROUP
WOS关键词G-PROTEIN ; BETA-ARRESTIN ; REGULATED KINASE ; SPLICE VARIANTS ; EXPRESSION ; PATHWAYS ; PARADIGMS ; MECHANISM ; MAPK ; SRC
原始文献类型Article
引用统计
文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/78889
专题生命科学与技术学院_硕士生
生命科学与技术学院_特聘教授组_徐华强组
通讯作者Xu, H. Eric; Jiang, Yi
作者单位
1.Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, VARI SIMM Ctr,Ctr Struct & Funct Drug Targets, Shanghai 201203, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
4.Van Andel Res Inst, Lab Struct Sci, Grand Rapids, MI 49503 USA
通讯作者单位生命科学与技术学院
推荐引用方式
GB/T 7714
Liu, Ping,Yin, Yu-ling,Wang, Ting,et al. Ligand-induced activation of ERK1/2 signaling by constitutively active G(s)-coupled 5-HT receptors[J]. ACTA PHARMACOLOGICA SINICA,2019,40(9):1157-1167.
APA Liu, Ping.,Yin, Yu-ling.,Wang, Ting.,Hou, Li.,Wang, Xiao-xi.,...&Jiang, Yi.(2019).Ligand-induced activation of ERK1/2 signaling by constitutively active G(s)-coupled 5-HT receptors.ACTA PHARMACOLOGICA SINICA,40(9),1157-1167.
MLA Liu, Ping,et al."Ligand-induced activation of ERK1/2 signaling by constitutively active G(s)-coupled 5-HT receptors".ACTA PHARMACOLOGICA SINICA 40.9(2019):1157-1167.
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