Effects of MAP kinase cascade inhibitors on the MKK5/ERK5 pathway

被引:225
作者
Mody, N
Leitch, J
Armstrong, C
Dixon, J
Cohen, P
机构
[1] Univ Dundee, Sch Life Sci, MRC, Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Sch Life Sci, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
基金
英国医学研究理事会;
关键词
mitogen-activated protein kinase; mitogen-activated protein kinase kinase 5; extracellular signal-regulated kinase 5; BMK1; PD184352;
D O I
10.1016/S0014-5793(01)02651-5
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
Antibodies that recognise the active phosphorylated forms of mitogen-activated protein kinase (MAPK) kinase 5 (MKK5) and extracellular signal-regulated kinase 5 (ERK5) in untransfected cells have been exploited to show that the epidermal growth factor (EGF)-induced activation of MKK5 and ERK5 occurs subsequent to the activation of ERK1 and ERK2 in HeLa cells. The drugs U0126 and PD184352, which prevent the activation of MKK1 (and hence the activation of ERK1/ERK2), also prevent the activation of MKK5, although higher concentrations are required. Our studies define physiological targets of the MKK5/ERK5 pathway as proteins whose phosphorylation is largely prevented by 10 muM PD184352, but unaffected by 2 muM PD184352. Surprisingly, 2 muM PD184352 prolongs the activation of MKK5 and ERK5 induced by EGF or H2O2, indicating negative control of the MKK5/ERK5 pathway by the classical MAPK cascade. Our results also indicate that ERK5 is not a significant activator of MAPK-activated protein kinase-1/RSK in HeLa cells. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:21 / 24
页数:4
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