Substance P-induced activation of p42/44 mitogen-activated protein kinase associated with cell proliferation in human tracheal smooth muscle cells

被引:29
作者
Yang, CM
Hsiao, LD
Chien, CS
Lin, CC
Luo, SF
Wang, CC
机构
[1] Chang Gung Univ, Coll Med, Dept Physiol & Pharmacol, Tao Yuan, Taiwan
[2] Chang Gung Univ, Dept Internal Med, Tao Yuan, Taiwan
关键词
cell proliferation; MAPK; protein kinase C; substance P; tyrosine kinase;
D O I
10.1016/S0898-6568(02)00039-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Substance P (SP) released from sensory nerve endings in the airways induces several responses including cell proliferation. However, the mechanisms were not completely understood in tracheal smooth muscle cells (TSMCs). We therefore investigated the effect of SP on cell proliferation and activation of p42/p44 mitogen-activated protein kinase (MAPK) in these cells. SP stimulated [H-3]thymidine incorporation and p42/p44 MAPK phosphorylation in a time- and concentration-dependent manner in TSMCs. Both DNA synthesis and phosphorylation of MAPK in response to SP were attenuated by pretreatment with pertussis toxin, genistein, D609, U73122, staurosporine, removal of Ca2+ by BAPTA/AM plus EGTA, PD98059, and SB202190. Furthermore, overexpression of dominant negative mutants, H-Ras-15A and Raf-N4, significantly suppressed p42/p44 MAPK activation induced by SP and PDGF-BB. These results conclude that the mitogenic effect of SP was mediated through the activation of Ras/Raf/MEK/MAPK pathway, which was modulated by PC-PLC, PI-PLC, Ca2+, and PKC in cultured human TSMCs. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:913 / 923
页数:11
相关论文
共 49 条
[21]   A DIVERGENCE IN THE MAP KINASE REGULATORY NETWORK DEFINED BY MEK KINASE AND RAF [J].
LANGECARTER, CA ;
PLEIMAN, CM ;
GARDNER, AM ;
BLUMER, KJ ;
JOHNSON, GL .
SCIENCE, 1993, 260 (5106) :315-319
[22]   Mechanisms of thrombin-induced MAPK activation associated with cell proliferation in human cultured tracheal smooth muscle cells [J].
Lin, CC ;
Shyr, MH ;
Chien, CS ;
Wang, CC ;
Chiu, CT ;
Hsiao, LD ;
Yang, CM .
CELLULAR SIGNALLING, 2001, 13 (04) :257-267
[23]   Linkage of G protein-coupled receptors to the MAPK signaling pathway through PI 3-kinase gamma [J].
LopezIlasaca, M ;
Crespo, P ;
Pellici, PG ;
Gutkind, JS ;
Wetzker, R .
SCIENCE, 1997, 275 (5298) :394-397
[24]   SUBSTANCE-P ACTIVATION OF RHEUMATOID SYNOVIOCYTES - NEURAL PATHWAY IN PATHOGENESIS OF ARTHRITIS [J].
LOTZ, M ;
CARSON, DA ;
VAUGHAN, JH .
SCIENCE, 1987, 235 (4791) :893-895
[25]   A SUBSTANCE-P ANTAGONIST INHIBITS VAGALLY INDUCED INCREASE IN VASCULAR-PERMEABILITY AND BRONCHIAL SMOOTH-MUSCLE CONTRACTION IN THE GUINEA-PIG [J].
LUNDBERG, JM ;
SARIA, A ;
BRODIN, E ;
ROSELL, S ;
FOLKERS, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (04) :1120-1124
[26]  
Lundberg JM, 1996, PHARMACOL REV, V48, P113
[27]  
Luo WH, 1996, CANCER RES, V56, P4983
[28]   TACHYKININ RECEPTORS AND TACHYKININ RECEPTOR ANTAGONISTS [J].
MAGGI, CA ;
PATACCHINI, R ;
ROVERO, P ;
GIACHETTI, A .
JOURNAL OF AUTONOMIC PHARMACOLOGY, 1993, 13 (01) :23-93
[29]   RAS TARGET PROTEINS IN EUKARYOTIC CELLS [J].
MARSHALL, MS .
FASEB JOURNAL, 1995, 9 (13) :1311-1318
[30]  
NEIBER K, 1992, J ALLERGY CLIN IMMUN, V90, P646