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纸质出版:2016
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丁长钰,龙宇鹏,杨永军,郑江.氯喹通过上调泛素-蛋白酶体相关分子表达抑制LPS活化巨噬细胞的实验研究[J].陆军军医大学学报(原第三军医大学学报),2016,38(10):1111-1115.
Ding Changyu,Long Yupeng,Yang Yongjun,Zheng Jiang.Chloroquine inhibits LPS-induced macrophage activation through up-regulation of ubiquitin-proteasome system related molecules[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(10):1111-1115.
丁长钰,龙宇鹏,杨永军,郑江.氯喹通过上调泛素-蛋白酶体相关分子表达抑制LPS活化巨噬细胞的实验研究[J].陆军军医大学学报(原第三军医大学学报),2016,38(10):1111-1115. DOI:
Ding Changyu,Long Yupeng,Yang Yongjun,Zheng Jiang.Chloroquine inhibits LPS-induced macrophage activation through up-regulation of ubiquitin-proteasome system related molecules[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(10):1111-1115. DOI:
目的 观察氯喹(chloroquine
CQ)对脂多糖/内毒素(lipopolysaccharide/endotoxin
LPS)刺激的巨噬细胞中泛素-蛋白酶体系统(ubiquitin-proteasome system
UPS)相关分子A20、TRIM33和USP28表达的影响。 方法 应用LPS刺激小鼠Raw264.7细胞,荧光定量PCR检测酸化抑制剂CQ对LPS诱导锌指蛋白A20、泛素连接酶TRIM33和泛素特异性蛋白酶USP28的mRNA表达,Western blot检测CQ对LPS诱导A20和TRIM33的蛋白表达。应用siRNA转染技术沉默A20,荧光定量PCR检测CQ对LPS诱导炎性细胞因子TNF的mRNA表达。 结果 与LPS对照组比较,经CQ预处理的Raw264.7细胞中,A20、TRIM33、USP28的mRNA表达均显著上调[(3.197±0.013) vs (1.292±0.009)
(1.627±0.113) vs (0.797±0.083)
(1.387±0.144) vs (0.742±0.061)
P0.05],A20和TRIM33的蛋白表达也同样上调。采用siRNA干扰A20基因表达,则CQ预处理组细胞中LPS诱导的TNF-α mRNA表达显著上调[(7.650±0.113) vs (4.145±0.120)
P0.01]。 结论 CQ可显著上调LPS活化的巨噬细胞中泛素化相关分子A20、TRIM33和USP28的表达,而干扰A20基因表达可显著上调LPS活化Raw264.7细胞中TNF-α的mRNA表达,提示泛素-蛋白酶体系统及其相关分子参与CQ抑制LPS-TLR4信号通路的活化。
Objective To determine the effect of chloroquine (CQ) on the expression of ubiquitin-proteasome system (UPS)-related molecules A20
TRIM33 and USP28 in LPS-stimulated Raw264.7 cells and the role of A20 in CQ-pretreated activated Raw264.7 cells. Methods The mRNA expression levels of zine finger protein A20
E3 ubiquitin ligase TRIM33 and ubiquitin-specific protease USP28 in CQ-pretreated LPS-activated Raw264.7 cells were measured by real-time PCR
and Western blotting was used to detect these protein expressions. siRNA transfection was used to silence A20
and TNF-α mRNA expression in CQ-pretreated LPS-activated Raw264.7 cells was tested by real-time PCR. Results The mRNA expression levels of A20
TRIM33 and USP28 in CQ-pretreated activated Raw264.7 cells were significantly increased compared with LPS treatment only (3.197±0.013 vs 1.292±0.009
1.627±0.113 vs 0.797±0.083
1.387±0.144 vs 0.742±0.061
P0.05). The protein expression levels of A20 and TRIM33 in CQ-treated cells were significantly increased. TNF-α mRNA expression was up-regulated in CQ-pretreated cells after siRNA interference of A20 (7.650±0.113 vs 4.145±0.120
P0.01). Conclusion CQ effectively enhances the mRNA and protein expression levels of A20
TRIM33 and USP28 in LPS-activated macrophages
and mRNA expression of TNF-α is significantly increased in LPS-activated Raw264.7 cells upon interference with A20
which indicates that UPS may play a role in the inhibitory effect of CQ on activating LPS-TLR4 signaling pathway.
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