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STAT1 Mediates Oroxylin A Inhibition of iNOS and Pro-Inflammatory Cytokines Expression in Microglial BV-2 Cells
被引:36
作者:
Liu, Po-Wen
[1
]
Chen, Mei-Fang
[3
,4
,5
]
Tsai, Andy Po-Yi
[1
]
Lee, Tony J. F.
[1
,2
,3
,6
]
机构:
[1] Tzu Chi Univ, Inst Pharmacol & Toxicol, Hualien, Taiwan
[2] Tzu Chi Univ, Dept Life Sci, Hualien, Taiwan
[3] Tzu Chi Univ, Coll Life Sci, Ctr Vasc Med, Hualien, Taiwan
[4] Buddhist Tzu Chi Gen Hosp, Dept Res, Hualien, Taiwan
[5] Tzu Chi Coll Technol, Hualien, Taiwan
[6] So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
来源:
PLOS ONE
|
2012年
/
7卷
/
12期
关键词:
NITRIC-OXIDE-SYNTHASE;
FACTOR-KAPPA-B;
15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2);
ACTIVATED MACROPHAGES;
MEMORY IMPAIRMENT;
GENE-EXPRESSION;
UP-REGULATION;
LIPOPOLYSACCHARIDE;
MECHANISMS;
DISEASE;
D O I:
10.1371/journal.pone.0050363
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Microglia-mediated inflammation is implicated in pathogenesis of neurodegenerative diseases. Oroxylin A, a flavonoid isolated from Scutellariae baicalensis, has been shown to ameliorate microglia activation-mediated neurodegeneration in vivo. The molecular mechanism underlying the inhibitory effects of oroxylin A on microglia activation, however, remains unknown. In the present study, effects of oroxylin A co-treated with lipopolysaccharide (LPS, 100 ng/ml) on LPS-induced activation of cultured microglial BV-2 cells were examined. Nitric oxide (NO) production was determined by Greiss method. Expression of inducible nitric oxide synthase (iNOS), interleukin (IL)-1 beta and IL-6 was assessed using real-time RT-PCR or Western blot analysis. Furthermore, activation of the nuclear factor kappa B (NF kappa B) and the signal transducer and activator of transcription 1 (STAT1) was examined by Western blot analysis and transcription factor DNA-binding activity assay. Our results indicated that oroxylin A (10-100 mu M) in a concentration-dependent manner inhibited LPS-induced NO production via blocking iNOS expression at both mRNA and protein levels without affecting the degradation rate of iNOS mRNA. Moreover, oroxylin A significantly attenuated LPS-induced late expression (20 hours after LPS challenge) of IL-1 beta and IL-6. Furthermore, oroxylin A significantly suppressed LPS-induced JAK2-mediated STAT1 phosphorylation without affecting LPS-induced NF kappa B-p65 nuclear translocation or NF kappa B-p65 DNA-binding activity. This is consistent with the finding that AG490, a specific JAK2 inhibitor, significantly inhibited LPS-induced STAT1 phosphorylation with almost completely diminished iNOS expression. These results suggest that oroxylin A, via suppressing STAT1 phosphorylation, inhibits LPS-induced expression of pro-inflammatory genes in BV-2 microglial cells. Citation: Liu P-W, Chen M-F, Tsai AP-Y, Lee TJF (2012) STAT1 Mediates Oroxylin A Inhibition of iNOS and Pro-Inflammatory Cytokines Expression in Microglial BV-2 Cells. PLoS ONE 7(12): e50363. doi:10.1371/journal.pone.0050363
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