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Oxidized Low-Density Lipoprotein Induces Matrix Metalloproteinase-9 Expression via a p42/p44 and JNK-Dependent AP-1 Pathway in Brain Astrocytes
被引:54
作者:
Wang, Hui-Hsin
[1
]
Hsieh, Hsi-Lung
[2
]
Wu, Cheng-Ying
[1
]
Sun, Chi-Chin
[3
]
Yang, Chuen-Mao
[1
]
机构:
[1] Chang Gung Univ, Dept Pharmacol, Tao Yuan, Taiwan
[2] Chang Gung Inst Technol, Div Basic Med Sci, Dept Nursing, Tao Yuan, Taiwan
[3] Chang Gung Mem Hosp, Dept Ophthalmol, Chilung, Taiwan
来源:
关键词:
oxLDL;
MMP-9;
JNK1/2;
ERK1/2;
PI3K/Akt;
ACTIVATED PROTEIN-KINASE;
SMOOTH-MUSCLE-CELLS;
RAT MESANGIAL CELLS;
N-TERMINAL KINASE;
FACTOR-KAPPA-B;
C-JUN;
TRANSCRIPTION FACTORS;
SIGNALING PATHWAYS;
ENDOTHELIAL-CELLS;
REGULATED KINASE;
D O I:
10.1002/glia.20732
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Upregulation of matrix metalloproteinases (MMPs), especially MMP-9, by oxidized low-density lipoprotein (oxLDL) is implicated in many inflammatory diseases including brain injury. However, the signaling mechanisms underlying oxLDL-induced MMP-9 expression in astrocytes largely remain unknown. Here we report that oxLDL induces expression of proMMP-9 via a MAPK-dependent AP-1 activation in rat brain astrocyte (RBA)-1 cells. Results revealed by gelatin zymography, RT-PCR, and Western blotting analyses showed that oxLDL-induced proMMP-9 gene expression was mediated through Akt, JNK1/2, and p42/p44 MAPK phosphorylation in RBA-1. cells. These responses were attenuated by inhibitors of PI3K (LY294002), JNK (SP600125), and p42/p44 MAPK (PD98059), or transfection with dominant negative mutants and short hairpin RNA. Moreover, we demonstrated that AP-1 (i.e., c-Fos/c-Jun) is crucial for oxLDL-induced proMMP-9 expression which was attenuated by pretreatment with AP-1 inhibitor (curcumin). The regulation of MMP-9 gene transcription by AP-1 was confirmed by oxLDL-stimulated MMP-9 luciferase activity which was totally lost in cells transfected with the AP-1. binding site-mutated MMP-9 promoter construct (mt-AP1-MMP-9). These results suggested that oxLDL-induced proMMP-9 expression is mediated through PI3K/Akt, JNK1/2, and p42/p44 MAPK leading to AP-1 activation. Understanding the regulatory mechanisms underlying oxLDL-induced MMP-9 expression in astrocytes might provide a new therapeutic strategy of brain injuries and diseases. (C) 2008 Wiley-Liss, Inc.
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页码:24 / 38
页数:15
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