[放线共生放线杆菌脂多糖诱导兔不同器官单核细胞/巨噬细胞产生细胞因子的差异表达]

[Different expression of cytokines induced by Actinobacillus actinomycetemcomitans lipopolysaccharide in monocytes/macrophages from different organs of rabbits].

作者信息

Huang Min, Li Hou-xuan, Luo Lan, Chen Shuai, Li Yan-fen, Yan Fu-hua

机构信息

Fujian Medical University, Fuzhou, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2013 Mar;48(3):155-60.

DOI:
Abstract

OBJECTIVE

To investigate the expression of cytokines induced by Actinobacillus actinomycetemcomitans lipopolysaccharide (Aa-LPS) in monocytes/macrophages from different organs of rabbits.

METHODS

The peripheral mononuclear cells (Mo), alveolar macrophages (AM), peritoneal macrophages (PM) and Kupffer cells (KC) from five New Zealand rabbits were isolated respectively. Then the cells from different organs were stimulated with Escherichia coli (Ec)-LPS or Aa-LPS at the dose of 1 mg/L. After culture for 24 hours, the expression of tumor necrosis factor-α (TNF-α), interleukin (IL)6, IL-1β, IL-8 mRNA and protein were determined by real-time PCR and enzyme-linked immunosorbent assay respectively.

RESULTS

The monocytes/macrophages challenged by Ec-LPS or Aa-LPS expressed more cytokines both in mRNA and protein levels compared with the controls (P < 0.05). Among them, AM displayed the highest respond when encount with Aa-LPS, with the TNF-α, IL-6, IL-1β, IL-8 mRNA relative levels were (0.4719 ± 0.0171), (2.7895 ± 0.0669), (5.1527 ± 0.1190), (3.6785 ± 0.1836) and the proteins concentrations were (82.2 ± 5.4), (40.2 ± 2.0), (50 308.3 ± 445.0), (35 305.3 ± 1480.9) ng/L respectively. And the inducibility of Aa-LPS was stronger than that of Ec-LPS (P < 0.05). Meanwhile the cells from different organs showed discrepant response when exposed to Aa-LPS (P < 0.05). The results showed their abilities to secrete cytokines were in the sequence of AM > Mo > KC > PM.

CONCLUSIONS

Aa-LPS influenced the expression of cytokines in monocytes/macrophages from different organs of rabbits.

摘要

目的

研究伴放线放线杆菌脂多糖(Aa-LPS)诱导的细胞因子在兔不同器官单核细胞/巨噬细胞中的表达。

方法

分别分离5只新西兰兔的外周血单个核细胞(Mo)、肺泡巨噬细胞(AM)、腹腔巨噬细胞(PM)和库普弗细胞(KC)。然后用1mg/L剂量的大肠杆菌(Ec)-LPS或Aa-LPS刺激来自不同器官的细胞。培养24小时后,分别采用实时荧光定量PCR和酶联免疫吸附测定法检测肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6、IL-1β、IL-8 mRNA和蛋白的表达。

结果

与对照组相比,经Ec-LPS或Aa-LPS刺激的单核细胞/巨噬细胞在mRNA和蛋白水平上均表达更多的细胞因子(P<0.05)。其中,AM在接触Aa-LPS时反应最强,TNF-α、IL-6、IL-1β、IL-8 mRNA相对水平分别为(0.4719±0.0171)、(2.7895±0.0669)、(5.1527±0.1190)、(3.6785±0.1836),蛋白浓度分别为(82.2±5.4)、(40.2±2.0)、(50 308.3±445.0)、(35 305.3±1480.9)ng/L。且Aa-LPS的诱导能力强于Ec-LPS(P<0.05)。同时,不同器官的细胞在接触Aa-LPS时表现出不同的反应(P<0.05)。结果显示它们分泌细胞因子的能力顺序为AM>Mo>KC>PM。

结论

Aa-LPS影响兔不同器官单核细胞/巨噬细胞中细胞因子的表达。

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