首页> 外文期刊>Journal of Huazhong University of Science and Technology >Role of Activator Protein-1 in the Transcription of InterIeukin-5 Gene Regulated by Protein Kinase C Signal in Asthmatic Human T Lymphocytes
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Role of Activator Protein-1 in the Transcription of InterIeukin-5 Gene Regulated by Protein Kinase C Signal in Asthmatic Human T Lymphocytes

机译:激活蛋白-1在哮喘人T淋巴细胞中蛋白激酶C信号调控的InterIeukin-5基因转录中的作用

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In order to explore the role of activator protein-1 (AP-1) in the transcription of interleu-kin-5 (IL-5) gene regulated by protein kinase C (PKC) signal in peripheral blood T lymphocytes from asthmatic patient, T lymphocytes were isolated and purified from peripheral blood of each asthmatic patient. The T lymphocytes were randomly divided into 4 groups: group A (blank control), group B (treated with PKC agonist phorbol 12-myristate 13-acetate (PMA)), Group C (treated with PMA and AP-1 cis-element decoy oligodeoxynucleotides (decoy ODNs)), and group D (treated with PMA and AP-1 mutant decoy ODNs). The ODNs were transfected into the T cells of group C and D by cation liposome respectively. Reverse transcription-polymerase chain reaction (RT-PCR) was employed to assess IL-5 mRNA expression, and electrophoretic mobility shift assays (EMSA) for the activation of AP-1. The results showed that the activation of AP-1 (88 003. 58 +- 1 626. 57) and the expression of IL-5 mRNA (0. 8300 +- 0. 0294) in T lymphocytes stimulated with PMA were significantly higher than these in blank control (20 888. 47 +- 1103. 56 and 0. 3050 +- 0. 0208, respectively, P < 0. 01), while the indexes (23 219. 83 +- 1 024. 86 and 0. 3425 +- 0. 0171 respectively) of T lymphocytes stimulated with PMA and AP-1 decoy ODNs were significantly inhibited, as compared with group B (P < 0. 01). The indexes (87 107. 41 ± 1 342. 92 and 0. 8225 ± 0. 0222, respectively) in T lymphocytes stimulated with PMA and AP-1 mutant decoy ODNs did not exhibit significant changes, as compared with group B (P > 0. 05). The significant positive correlation was found between the activation of AP-1 and the expression of IL-5 mRNA (P < 0. 01). It was concluded that AP-1 might participate in the signal transduction of PKC-triggered transcription of IL-5 gene in asthmatic T lymphocytes. This suggests the activation of PKC/AP-1 signal transduction cascade of T lymphocytes may play an important role in the pathogenesis of asthma.
机译:为了探讨激活蛋白-1(AP-1)在哮喘患者外周血T淋巴细胞中由蛋白激酶C(PKC)信号调节的白介素5(IL-5)基因转录中的作用从每位哮喘患者的外周血中分离并纯化了淋巴细胞。 T淋巴细胞随机分为4组:A组(空白对照组),B组(用PKC激动剂佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)处理),C组(用PMA和AP-1顺式诱饵治疗)寡脱氧核苷酸(诱饵ODN)和D组(用PMA和AP-1突变诱饵ODN处理)。将ODN分别通过阳离子脂质体转染到C和D组的T细胞中。逆转录-聚合酶链反应(RT-PCR)用于评估IL-5 mRNA的表达,电泳迁移率变动分析(EMSA)用于激活AP-1。结果表明,PMA刺激的T淋巴细胞中AP-1的激活(88 003. 58 +-1 626. 57)和IL-5 mRNA的表达(0. 8300 +-0. 0294)显着高于PMA刺激的T淋巴细胞。它们分别在空白控件中(20 888. 47 +1103。56和0. 3050 +/- 0. 0208,P <0. 01),而索引(23 219. 83 +1.024。86和0。与B组相比,PMA和AP-1诱饵ODNs刺激的T淋巴细胞分别显着抑制了3425±0. 0171)(P <0. 01)。与B组相比,PMA和AP-1突变诱饵ODNs刺激的T淋巴细胞中的指标(分别为87107. 41±1342. 92和0. 8225±0. 0222)没有显示出明显的变化(P> 0. 05)。发现AP-1的激活与IL-5 mRNA的表达之间存在显着的正相关(P <0. 01)。结论是AP-1可能参与了哮喘T淋巴细胞中PKC触发的IL-5基因转录的信号转导。这提示T淋巴细胞PKC / AP-1信号转导级联的激活可能在哮喘发病中起重要作用。

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