Relaxin signalling in THP-1 cells uses a novel phosphotyrosine-dependent pathway

被引:16
作者
Anand-Ivell, Ravinder
Heng, Kee
Bartsch, Olaf
Ivell, Richard [1 ]
机构
[1] Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA 5005, Australia
[2] Univ Hamburg, Inst Hormone & Fertil Res, D-20251 Hamburg, Germany
关键词
relaxin; tyrphostin; LGR7; adenylate cyclase; protein kinase A; PROTEIN-KINASE-C; CYCLIC ADENOSINE-3'; 5'-MONOPHOSPHATE; ADENYLYL-CYCLASE; RECEPTORS; IDENTIFICATION; INHIBITION; ACTIVATION; 3-KINASE; PHOSPHODIESTERASE; RELAXIN-3/INSL7;
D O I
10.1016/j.mce.2007.04.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The heterodimeric peptide hormone relaxin acts through the novel G-protein coupled receptor LGR7 to elicit the production of cAMP in the human monocyte cell line THP-1. The very small number of receptors on the cell surface, and the lack of response in cell membranes imply the involvement of a cytoplasmic signal amplification process. Here we show that this process comprises a novel and specific tyrosine kinase activity close to the receptor, and involves neither protein kinase A, mitogen-activated protein kinase, nor phosphoinositide-3 kinase activities as major upstream components. Furthermore, this novel involvement of a tyrosine kinase activity is cell-type dependent, being largely absent from LGR7-transfected HEK293T cells, and receptor-dependent; vasoactive intestinal peptide or isoproterenol signalling in the same cells does not require this tyrosine kinase activity. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 34 条
[1]   Relaxin activates the L-arginine nitric oxide pathway in vascular smooth muscle cells in culture [J].
Bani, D ;
Failli, P ;
Bello, MG ;
Thiemermann, C ;
Sacchi, TB ;
Bigazzi, M ;
Masini, E .
HYPERTENSION, 1998, 31 (06) :1240-1247
[2]   Phosphodiesterase 4 inhibition synergizes with relaxin signaling to promote decidualization of human endometrial stromal cells [J].
Bartsch, O ;
Bartlick, B ;
Ivell, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) :324-334
[3]  
Bartsch O, 2001, RELAXIN 2000, P309
[4]   Relaxin signalling links tyrosine phosphorylation to phosphodiesterase and adenylyl cyclase activity [J].
Bartsch, O ;
Bartlick, B ;
Ivell, R .
MOLECULAR HUMAN REPRODUCTION, 2001, 7 (09) :799-809
[5]   International union of pharmacology LVII: Recommendations for the nomenclature of receptors for relaxin family peptides [J].
Bathgate, RA ;
Ivell, R ;
Sanborn, BM ;
Sherwood, OD ;
Summers, RJ .
PHARMACOLOGICAL REVIEWS, 2006, 58 (01) :7-31
[6]   Evidence for inhibition by protein kinase A of receptor/Gαq phospholipase C (PLC) coupling by a mechanism not involving PLCβ2 [J].
Dodge, KL ;
Sanborn, BM .
ENDOCRINOLOGY, 1998, 139 (05) :2265-2271
[7]   Identification of the pregnancy hormone relaxin as glucocorticoid receptor agonist [J].
Dschietzig, T ;
Bartsch, C ;
Stangl, V ;
Baumann, G ;
Stangl, K .
FASEB JOURNAL, 2004, 18 (11) :1536-+
[8]   CYCLIC-AMP RESPONSE TO RECOMBINANT HUMAN RELAXIN BY CULTURED HUMAN ENDOMETRIAL CELLS - A SPECIFIC AND HIGH THROUGHPUT INVITRO BIOASSAY [J].
FEI, DTW ;
GROSS, MC ;
LOFGREN, JL ;
MORAWORMS, M ;
CHEN, AB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (01) :214-222
[9]   Relaxin stimulates leukocyte adhesion and migration through a relaxin receptor LGR7-dependent mechanism [J].
Figueiredo, KA ;
Mui, AL ;
Nelson, CC ;
Cox, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (06) :3030-3039
[10]   Relaxin family peptide receptors RXFP1 and RXFP2 modulate cAMP signaling by distinct mechanisms [J].
Halls, Michelle L. ;
Bathgate, Ross A. D. ;
Summers, Roger J. .
MOLECULAR PHARMACOLOGY, 2006, 70 (01) :214-226