ShanghaiTech University Knowledge Management System
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 (IF:6.9[JCR-2023],7.6[5-Year]) |
ISSN | 1671-4083 |
卷号 | 40期号:9页码:1157-1167 |
发表状态 | 已发表 |
DOI | 10.1038/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 | 正在获取...
|
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. |
条目包含的文件 | ||||||
文件名称/大小 | 文献类型 | 版本类型 | 开放类型 | 使用许可 |
修改评论
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。