Crosstalk of EGF-directed MAPK signalling pathways and its potential role on EGF-induced cell proliferation and COX-2 expression in human mesenchymal stem cells

被引:22
|
作者
Sabri, Abdullah [2 ]
Ziaee, Abed-Ali [2 ]
Ostad, Seyed Nasser
Alimoghadam, Kamran [3 ]
Ghahremani, Mohammad Hossein [1 ]
机构
[1] Univ Tehran Med Sci, Fac Pharm, Dept Pharmacol Toxicol, Tehran 141556451, Iran
[2] Univ Tehran, Inst Biochem & Biophys, Tehran 141556451, Iran
[3] Univ Tehran Med Sci, Shariati Hosp, Hematol Oncol & BMT Res Ctr, Tehran, Iran
关键词
mesenchymal stem cells; epidermal growth factor; ERK; AKT; JNK; p38; COX-2; ACTIVATED PROTEIN-KINASE; EPIDERMAL-GROWTH-FACTOR; CYCLOOXYGENASE-2; EXPRESSION; P38; RECEPTOR; DIFFERENTIATION; TRANSDUCTION; ASTROCYTES; EXPANSION; ALPHA;
D O I
10.1002/cbf.1720
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
Epidermal growth factor (EGF) promotes proliferation in human mesenchymal stem cells (hMSCs) during in vitro propagation. In this study, we investigated the effects of PI3K/AKT, ERK1/2, P38 and JNK on EGF signalling in hMSCs. The effects of EGF on MAPKs and PI3K/AKT crosstalk were investigated by immunoblotting; cyclooxygenase-2 (COX-2) expression was studied by real-time RT-PCR; and cell proliferation was evaluated by methylthiazolyl tetrazolium bromide assay. Our results showed that EGF immediately activated all four pathways, induced proliferation and increased COX-2 expression. Interestingly, inhibition of PI3K/AKT-enhanced EGF-stimulated ERK1/2 activity, and inhibition of ERK1/2 and JNK reduced AKT phosphorylation. Furthermore, EGF-induced proliferation as well as EGF-augmented COX2 expression was hindered by ERK1/2 and p38 inhibitors. The results of this study provide evidences to be used in extended proliferation of hMSCs for cell therapy. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:64 / 70
页数:7
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