Molecular and functional characterization of adipokinetic hormone receptor and its peptide ligands in Bombyx mori

被引:36
|
作者
Zhu, Chenggang [1 ]
Huang, Haishan [1 ]
Hua, Rongsheng [2 ]
Li, Guo [1 ]
Yang, Dong [1 ]
Luo, Jiansong [3 ]
Zhang, Cunxin [1 ]
Shi, Liangen [2 ]
Benovic, Jeffrey L. [3 ]
Zhou, Naiming [1 ]
机构
[1] Zhejiang Univ, Inst Biochem, Coll Life Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Anim Sci, Hangzhou 310029, Zhejiang, Peoples R China
[3] Thomas Jefferson Univ, Dept Biochem, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
来源
FEBS LETTERS | 2009年 / 583卷 / 09期
基金
中国国家自然科学基金;
关键词
Adipokinetic hormone; Signal transduction; Receptor; G protein; Internalization; Mitogen-activated protein kinase; Bombyx mori; ACTIVATED PROTEIN-KINASE; CORPORA CARDIACA; LOCUSTA-MIGRATORIA; MANDUCA-SEXTA; FAT-BODY; FAMILY; IDENTIFICATION; MEMBER; NEUROPEPTIDE; MECHANISMS;
D O I
10.1016/j.febslet.2009.03.060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuropeptides of the adipokinetic hormone (AKH) family are among the best studied hormone peptides, but its signaling pathways remain to be elucidated. In this study, we molecularly characterized the signaling of Bombyx AKH receptor (AKHR) and its peptide ligands in HEK293 cells. In HEK293 cells stably expressing AKHR, AKH1 stimulation not only led to a ligand concentration dependent mobilization of intracellular Ca2+ and cAMP accumulation, but also elicited transient activation of extracellular signal-regulated kinase 1/2 (ERK1/2) pathway. We observed that AKH receptor was rapidly internalized after AKH1 stimulation. We further demonstrated that AKH2 exhibited high activities in cAMP accumulation and ERK1/2 activation on AKHR comparable to AKH1, whereas AKH3 was much less effective. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1463 / 1468
页数:6
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