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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.
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页码:83 / 93
页数:11
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