首页> 美国卫生研究院文献>Journal of Toxicology >Proliferation and TH1/TH2 Cytokine Production in Human Peripheral Blood Mononuclear Cells after Treatment with Cypermethrin and Mancozeb In Vitro
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Proliferation and TH1/TH2 Cytokine Production in Human Peripheral Blood Mononuclear Cells after Treatment with Cypermethrin and Mancozeb In Vitro

机译:氯氰菊酯和Mancozeb体外处理后人外周血单个核细胞中增殖和TH1 / TH2细胞因子的产生

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摘要

In recent times, human cell-based assays are gaining attention in assessments of immunomodulatory effects of chemicals. In the study here, the possible effects of cypermethrin and mancozeb on lymphocyte proliferation and proinflammatory (tumor necrosis factor (TNF-) α) and immunoregulatory cytokine (interferon- (IFN-) γ, interleukins (IL) 2, 4, 6, and 10) formation in vitro were investigated. Human peripheral blood mononuclear cells (PBMC) were isolated and exposed for 6 hr to noncytotoxic doses (0.45–30 µM) of cypermethrin or mancozeb in the presence of activating rat S9 fraction. Cultures were then further incubated for 48 or 72 hr in fresh medium containing phytohemagglutinin (10 µg/mL) to assess, respectively, effects on cell proliferation (BrdU-ELISA method) and cytokine formation (flow cytometric bead immunoassays). Mancozeb induced dose-dependent increases in lymphocyte proliferation, inhibition of production of TNFα and the TH2 cytokines IL-6 and IL-10, and an increase in IFNγ (TH1 cytokine) production (at least 2-fold compared to control); mancozeb also induced inhibition of IL-4 (TH2) and stimulated IL-2 (TH1) production, albeit only in dose-related manners for each. In contrast, cypermethrin exposure did not cause significant effects on proliferation or cytokine profiles. Further studies are needed to better understand the functional significance of our in vitro findings.
机译:近年来,基于人体细胞的测定法在评估化学物质的免疫调节作用方面受到关注。在这里的研究中,氯氰菊酯和代森锰锌对淋巴细胞增殖和促炎(肿瘤坏死因子(TNF-)α)和免疫调节细胞因子(干扰素-(IFN-)γ,白介素(IL)2、4、6和10)研究了体外形成。分离人类外周血单核细胞(PBMC),并在活化的大鼠S9组分存在下,将其暴露于非细胞毒性剂量(0.45–30μM)的氯氰菊酯或代森锰锌6分钟。然后将培养物在含有植物血凝素(10μg/ mL)的新鲜培养基中进一步孵育48或72小时,以分别评估对细胞增殖的影响(BrdU-ELISA方法)和细胞因子的形成(流式细胞术珠粒免疫测定)。 Mancozeb诱导剂量依赖性增加淋巴细胞增殖,抑制TNFα和TH2细胞因子IL-6和IL-10的产生,以及增加IFNγ(TH1细胞因子)的产生(与对照相比至少2倍);曼考布也诱导了IL-4(TH2)的抑制并刺激了IL-2(TH1)的产生,尽管每种都以剂量相关的方式进行。相反,氯氰菊酯的暴露对增殖或细胞因子的分布没有明显影响。需要进一步研究以更好地了解我们体外研究结果的功能意义。

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