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第三军医大学西南医院肾科
纸质出版日期:2011,
网络出版日期:2011-10-30,
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卓燕, 余荣杰, 赵洪雯, 等. 阿托伐他汀抑制ApoE-/-小鼠腹腔巨噬细胞LPS刺激下NF-κB p65核转位[J]. 陆军军医大学学报, 2011,33(20):2120-2123.
ZHUO YAN, YU RONGJIE, ZHOU HONGWEN, et al. Atorvastatin suppresses nuclear translocation of NF-κB p65 in LPS-induced abdominal macrophage of ApoE-/- mouse. [J]. Journal of army medical university, 2011, 33(20): 2120-2123.
卓燕, 余荣杰, 赵洪雯, 等. 阿托伐他汀抑制ApoE-/-小鼠腹腔巨噬细胞LPS刺激下NF-κB p65核转位[J]. 陆军军医大学学报, 2011,33(20):2120-2123. DOI:
ZHUO YAN, YU RONGJIE, ZHOU HONGWEN, et al. Atorvastatin suppresses nuclear translocation of NF-κB p65 in LPS-induced abdominal macrophage of ApoE-/- mouse. [J]. Journal of army medical university, 2011, 33(20): 2120-2123. DOI:
目的 观察阿托伐他汀对脂多糖(lipopolysaccharides,LPS)刺激载脂蛋白E基因缺陷(apolipoprotein E knockout,ApoE
-/-
)小鼠腹腔巨噬细胞NF-κB p65核转位的影响。 方法 采用LPS 10 ng/ml刺激分离纯化的ApoE
-/-
小鼠腹腔巨噬细胞,并给予1、5、10 μmol/L不同浓度的阿托伐他汀进行干预,免疫荧光染色结合激光共聚焦显微镜观察NF-κB p65核转位,Western blot法检测NF-κB p65核内表达,ELASA法检测细胞上清液IL-6水平。 结果 激光共聚焦及Western blot均观察到阴性对照组核内NF-κB p65表达较低,其平均荧光强度为(3.71±0.26);阳性对照组核内NF-κB p65表达较阴性对照组显著增高[(16.12±1.28)
P
<0.05
]
;不同剂量阿托伐他汀干预组细胞核内NF-κB p65表达呈剂量依耐性逐渐降低,其平均荧光强度分别为(10.95±0.71)、(7.61±0.73)、(4.56±0.39)
差异具有统计学意义(
P
<
0.05);同时可发现药物干预组细胞上清液IL-6分泌量也呈剂量依耐性逐渐降低(
P
<0.05)。 结论 阿托伐他汀能抑制ApoE
-/-
小鼠腹腔巨噬细胞LPS刺激下NF-κB p65核转位及其随后炎性介质IL-6分泌。
Objective To determine the effects of atorvastatin on the translocation of NF-κB p65 into the nuclear induced by LPS in abdominal macrophage isolated from apolipoprotein E knockout (ApoE
-/-
) mouse. Methods Abdominal macrophage were isolated and purified from ApoE
-/-
mouse
and then cultivated
and treated by atorvastatin (10 μmol/L)
LPS (10 ng/ml)
and atorvastatin (1
5 and 10 μmol/L) combined with LPS treatment. The nuclear translocation of NF-κB p65 was observed by laser scanning confocal microscopy and Western blotting
while the IL-6 levels in culture supernatants was measured by ELASA. Results Laser scanning confocal microscopy and Western blotting showed that TRITC-labeled NF-κB p65 was mainly located in the plasma of macrophage and mildly expressed in the nuclear in atorvastatin group (3.71±0.26)
but was mainly located in the nuclei and strongly expressed in LPS group (16.12±1.28
P
<
0.05). When macrophage were cultivated and induced by LPS and different concentrations atorvastatin
NF-κB p65 was expressed in the nuclear in a negative dose-dependent manner (10.95±0.71
7.61±0.73
and 4.56±0.39
respectively
P
<
0.05). At the same time
the IL-6 levels in culture supernatants was also reduced in a negative dose-dependent manner in atorvastatin intervention groups(
P
<
0.05). Conclusion Atorvastatin inhibits the nuclear translocation of NF-κB p65 and secretion of inflammatory mediators IL-6 in abdominal macrophage of ApoE
-/-
mouse induced by LPS.
阿托伐他汀脂多糖巨噬细胞NF-κB p65小鼠基因敲除
atorvastatinlipopolysaccharidesabdominal macrophageNF-κB p65miceknockout
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