EGF family ligand-dependent phenotypic modulation of smooth muscle cells through EGF receptor

被引:41
作者
Yamanaka, Y
Hayashi, K
Komurasaki, T
Morimoto, S
Ogihara, T
Sobue, K
机构
[1] Osaka Univ, Grad Sch Med, Dept Neurosci D13, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Geriatr Med B6, Suita, Osaka 5650871, Japan
[3] Taisho Pharmaceut Co Ltd, Res Ctr, Omiya, Saitama 3308530, Japan
关键词
smooth muscle cell; phenotypic modulation; EGF family ligands; EGF-receptor family; ERK; p38MAPK;
D O I
10.1006/bbrc.2001.4385
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
The phenotypic modulation of smooth muscle cells (SMCs) is closely associated with the development and progression of various SMC diseases, We investigated the molecular mechanism of phenotypic modulation triggered by EGF family ligands using a primary culture system of differentiated SMCs. Among four EGF-receptor (EGFR) family members, the EGFR was solely activated by EGF, heparin-binding EGF (HB-EGF), transforming growth factor alpha (TGF alpha), epiregulin (ER), and betacellulin (BTC), resulting in induction of phenotypic modulation of SMCs, This effect was mediated through the coordinated activation of the extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (p38MAPK) pathways. These results suggest that EGF family ligand- and EGFR-triggered signaling pathways are critically involved in the phenotypic modulation of SMCs, (C) 2001 Academic Press.
引用
收藏
页码:373 / 377
页数:5
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