Activation of c-Jun N-terminal kinase 1 (JNK-1) after amino acid deficiency in HeLa cells

被引:10
作者
Aubel, C
Dehez, S
Chabanon, H
Seva, C
Ferrara, M
Brachet, P [1 ]
机构
[1] INRA, UR Nutr Cellulaire & Mol 238, F-63122 St Genes Champanelle, France
[2] CHU Rangueil, INSERM, U531, Grp Rech Biol & Pathol Digest, F-31054 Toulouse, France
关键词
signal transduction; mitogen-activated protein kinase; MAPK; nutrient starvation;
D O I
10.1016/S0898-6568(01)00159-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long-term amino acid starvation represents a form of metabolic stress which stimulates gene expression. Here we report that depriving HeLa cells for any one of a series of amino acids activates c-Jun N-terminal kinase-1 (JNK-1). In contrast, the other mitogen-activated protein kinases (MAPKs) ERK-1 and, to a lesser extent, p38 activities decreased under such conditions. In methionine- or leucine-deprived cells, JNK-1 activation occurred after 4 or 6 h, respectively, and reached a steady maximum of 5- to 7-fold over control cells afterwards. This activation was dependent on the amino acid concentration and it could be reversed by resupplying the complete medium. Limitation for all amino acids also augmented JNK-1 activity, whereas increased amino acid concentrations had an opposite effect. The free radical scavenging thiol antioxidant N-acetylcysteine (NAC) alleviated partially JNK-1 activation in amino acid-deprived cells. The data indicate that activation of JNK-1 by long-term amino acid deprivation may be mediated in part by oxidative stress. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:417 / 423
页数:7
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