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[流感病毒感染肺炎小鼠中与自然杀伤细胞介导的细胞毒性相关基因的筛选及两种中药抗病毒方剂的调控]

[Screening for genes associated with natural killer cell mediated cytotoxicity in pneumonia mice infected with influenza virus and regulation of two herbal anti-virus formulas].

作者信息

Lu Na-na, Liu Qi, Gu Li-gang, Zhou Xu-peng, Wu Jun, Qiu Ze-Ji, Zhang Hong-chun, Chao En-xiang, Zhang Yi

机构信息

Laboratory of Chinese Medicine on Viral Disease, Beijing University of Chinese Medicine, Basic Medical College, China.

出版信息

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2013 Jun;25(6):322-6. doi: 10.3760/cma.j.issn.2095-4352.2013.06.002.

Abstract

OBJECTIVE

To investigate the regulation of two herbal anti-virus formulas on gene expression profile associated with natural killer cell (NK cell) mediated cytotoxicity in pneumonia mice infected with influenza virus.

METHODS

According to random number table, 90 ICR mice were divided into nine groups with 10 mice in each group: normal group (N), model group (M), oseltamivir group (control group, C), low-dose, medium-dose and high-dose Shufeng Xuanfei formula groups (SL, SM, SH groups), and low-dose, medium-dose and high-dose Jiebiao Qingli formula groups (JL, JM, JH groups). The model of pneumonia was reproduced by nasal dropping influenza virus A (FM1) in mice. N group was given isotonic saline 0.05 ml in nasal drops. After 2 hours of model-building, C group was received 11.375 mg×kg⁻¹×d⁻¹ oseltamivir phosphate. Shufeng Xuanfei formula (mainly honeysuckle, forsythia and radix isatidis, etc.) with 3.76, 1.88 and 0.94 g×kg⁻¹×d were administrated to SH, SM and SL groups by gastric irrigation respectively. Jiebiao Qingli formula (mainly ephedra, gypsum, glycyrrhiza glabra, etc.) with 4.36, 2.18 and 1.09 g×kg⁻¹×d⁻¹ were administrated to JH, JM and JL groups by gastric irrigation respectively. In N and M groups, normal saline was administrated with gastric perfusion. Each group was in equal dose of 0.2 ml daily over a 4-day period. Total RNA in lung tissue of mice were extracted in each group, then gene chips were used to screen these RNA samples. Some genes involved NK cell mediated cytotoxicity were selected, with "I" representing of signal intensity. These candidate genes were verified by real-time fluorescent quantitation polymerase chain reaction (PCR) and Western blotting.

RESULTS

In the pathway of NK cell mediated cytotoxicity, M group up-regulated 43 genes expression, and 36, 29, 22, 21, 20 and 10 genes showed down-regulation in SM, JM, SL, JH, SH and JL groups, respectively. Apart from gene co-expression network in SH, SL, JH, JM and JL, SM also expressed other differential genes which SH, SL, JH, JM and JL did not. So medium-does Shufeng Xuanfei formula had the most significant regulation in gene expression of NK cell mediated cytotoxicity. By real-time PCR and Western blotting experiments showed that compared with the M group, mRNA and protein expression of tumor necrosis factor-α (TNF-α) in these two formula groups were significantly down-regulated, especially prominent in SM group and JM group (TNF-α mRNA: 1.07 ± 0.19, 1.19 ± 0.14 vs. 3.20 ± 0.56, both P<0.01).

CONCLUSIONS

Influenza viral replication in host cell, which means influenza antigens exposure in infected cells as target cells. NK cells recognize and exert cell mediated cytotoxic function against influenza antigens. Genes associated with NK cell mediated cytotoxicity in influenza infection were up-regulated. Shufeng Xuanfei and Jiebiao Qingli formulas could down-regulate these genes. The mechanism of down-regulated genes is that the number of influenza infected cells and NK cells activation decreases in treatment with two formulas.

摘要

目的

探讨两种中药抗病毒方剂对感染流感病毒的肺炎小鼠中与自然杀伤细胞(NK细胞)介导的细胞毒性相关基因表达谱的调控作用。

方法

将90只ICR小鼠按随机数字表法分为9组,每组10只:正常组(N)、模型组(M)、奥司他韦组(对照组,C)、疏风宣肺方低剂量、中剂量、高剂量组(SL、SM、SH组),解表清里方低剂量、中剂量、高剂量组(JL、JM、JH组)。采用滴鼻甲型流感病毒(FM1)复制小鼠肺炎模型。N组滴鼻给予0.05 ml等渗盐水。造模2小时后,C组给予11.375 mg×kg⁻¹×d⁻¹磷酸奥司他韦。SH、SM、SL组分别灌胃给予3.76、1.88、0.94 g×kg⁻¹×d的疏风宣肺方(主要含金银花、连翘、板蓝根等)。JH、JM、JL组分别灌胃给予4.36、2.18及1.09 g×kg⁻¹×d⁻¹的解表清里方(主要含麻黄、石膏、甘草等)。N组和M组灌胃给予生理盐水。每组每日等剂量0.2 ml,连续给药4天。提取各组小鼠肺组织总RNA,然后用基因芯片筛选这些RNA样本。选择一些参与NK细胞介导细胞毒性的基因,用“I”表示信号强度。这些候选基因通过实时荧光定量聚合酶链反应(PCR)和蛋白质印迹法进行验证。

结果

在NK细胞介导的细胞毒性途径中,M组43个基因表达上调,SM、JM、SL、JH、SH、JL组分别有36、29、22、21、20和10个基因表达下调。除SH、SL、JH、JM、JL组的基因共表达网络外,SM组还表达了SH、SL、JH、JM、JL组未表达的其他差异基因。因此,中剂量疏风宣肺方对NK细胞介导的细胞毒性基因表达调控作用最显著。实时PCR和蛋白质印迹实验表明,与M组相比,这两个方剂组肿瘤坏死因子-α(TNF-α)的mRNA和蛋白表达均显著下调,尤以SM组和JM组明显(TNF-α mRNA:1.07±0.19、1.19±0.14 vs. 3.20±0.56,均P<0.01)。

结论

流感病毒在宿主细胞内复制,意味着感染细胞中流感抗原作为靶细胞暴露。NK细胞识别并对流感抗原发挥细胞介导的细胞毒性作用。流感感染中与NK细胞介导的细胞毒性相关的基因上调。疏风宣肺方和解表清里方均可下调这些基因。下调基因的机制是两个方剂治疗后流感感染细胞数量及NK细胞活化减少。

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