4-hydroxynonenal signalling to apoptosis in isolated rat hepatocytes:: The role of PKC-δ

被引:24
作者
Castello, L
Marengo, B
Nitti, M
Froio, T
Domenicotti, C
Biasi, F
Leonarduzzi, G
Pronzato, MA
Marinari, UM
Poli, G
Chiarpotto, E
机构
[1] Univ Turin, Dept Clin & Biol Sci, I-10043 Orbassano, TO, Italy
[2] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
[3] Univ Turin, CNR, Dept Clin & Biol Sci, I-10043 Orbassano, TO, Italy
[4] Gaslini Inst, Genoa, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2005年 / 1737卷 / 2-3期
关键词
4-hydroxy-2,3-nonenal (HNE); protein kinase C; Jun N-terminal kinase; apoptosis;
D O I
10.1016/j.bbalip.2005.10.003
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
4-Hydroxynonenal, a significant aldehyde end product of membrane lipid peroxidation with numerous biochemical activities, has consistently been detected in various human diseases. Concentrations actually detectable in vivo (0.1 - 5 mu M) have been shown to up-regulate different genes and modulate various enzyme activities. In connection with the latter aspect, we show here that, in isolated rat hepatocytes, I PM 4-hydroxyrionenal selectively activates protein kinase C-6, involved in apoptosis of many cell types; it also induces very early activation of Jun N-terminal kinase, in parallel increasing activator protein-l DNA-bulding activity in a tune-dependent manner and triggering apoptosis after only 120 min treatment. These phenomena are likely protein kinase C-8-dependent, being significantly reduced or annulled by cell co-treatment with rottlerin, a selective inhibitor of protein kinase C-6. We suggest that 4-hydroxynonenal may induce apoptosis through activation of protein kinase C-6 and of Jun N-terminal kinase, and consequent up-regulation of activator protein-1 DNA binding. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 93
页数:11
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