Oxidative stress activates AMPK in cultured cells primarily by increasing cellular AMP and/or ADP

被引:125
作者
Auciello, F. Romana [1 ]
Ross, Fiona A. [1 ]
Ikematsu, Naoko [1 ]
Hardie, D. Grahame [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Cell Signalling & Immunol, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
AMP; ADP; AMP-activated protein kinase; Hydrogen peroxide; Oxidative stress; DEPENDENT PROTEIN-KINASE; TUMOR-SUPPRESSOR LKB1; UPSTREAM KINASE; ENERGY SENSOR; SIGNAL; PHOSPHORYLATION; MECHANISMS; CASCADE; TARGET; DRUGS;
D O I
10.1016/j.febslet.2014.07.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
AMPK is known to be activated by oxidative stress. Addition of glucose oxidase to cells generates H2O2 at a constant rate that is opposed by enzymic degradation, providing a good model for physiological oxidative stress. AMPK activation by glucose oxidase correlated with increases in cellular AMP:ATP and was greatly reduced in cells expressing an AMP-insensitive AMPK mutant, although a small degree of activation remained. The effects of increased AMP were partly due to inhibition of Thr172 dephosphorylation. These results suggest that changes in adenine nucleotides, rather than direct oxidative modification, are the major drivers of AMPK activation during oxidative stress. (C) 2014 The Authors. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:3361 / 3366
页数:6
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