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Effects of histamine and its antagonists on murine T-cells and bone marrow-derived dendritic cells

机译:组胺及其拮抗剂对小鼠T细胞和骨髓源性树突状细胞的影响

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Abstract: We determined the effects of histamine and its antagonists on the surface marker expression of dendritic cells (DCs) and the influence of lipopolysaccharide (LPS), histamine, and histamine receptor antagonists on DCs and T-cells. The bone marrow was extracted from the femurs and tibiae of 6- to 8-week-old female Balb/c mice and cultured in medium containing penicillin, streptomycin, L-glutamine, fetal calf serum, or granulocyte macrophage colony-stimulating factor (GM-CSF) alone or with interleukin (IL)-4. The cells received three different doses of LPS and histamine, plus three different doses of descarboethoxyloratadine (DCL). We assayed the supernatant for various cytokines. The spleen cells of DO11.10 mice?were examined by flow cytometry, which included labeling and sorting CD4+ T-cells, as well as coculture of DCs and T-cells with ovalbumin (OVA)323–339 peptide. Histamine or histamine plus DCL did not affect the expression of major histocompatibility complex class II, CD11c, CD11b, CD86, and CD80. However, GM-CSF increased the expression of all markers except CD80. Histamine increased interferon-γ production in GM-CSF + IL-4-cultured cells; it also enhanced IL-10 production, but suppressed IL-12 production in LPS-stimulated DCs with no DCL. Cimetidine inhibited IL-10 production and restored IL-12 secretion in LPS-treated DCs. LPS increased IL-10 and decreased IL-12 levels. GM-CSF + IL-4-generated DCs had a stronger stimulatory effect on DO11.10 T-cell proliferation than GM-CSF-generated DCs. Inducible costimulator ligand expression was higher in GM-CSF + IL-4- than in GM-CSF-generated DC groups after 2 days of coculture, but decreased 4 days later. IL-13 production was higher in bone marrow DCs generated with GM-CSF than in those generated with GM-CSF + IL-4. OVA-pulsed DCs and OVA-plus-DCL DCs showed increased IL-12 levels. OVA plus LPS increased both IL-10 and interferon-α. Although histamine or histamine receptor-1 antagonists did not influence DC LPS-driven maturation, they influenced cytokine production. LPS and GM-CSF influenced surface marker expression and cytokine production.
机译:摘要:我们确定了组胺及其拮抗剂对树突状细胞(DCs)表面标志物表达的影响,以及脂多糖(LPS),组胺和组胺受体拮抗剂对DC和T细胞的影响。从6至8周龄的Balb / c雌性小鼠的股骨和胫骨中提取骨髓,并在含有青霉素,链霉素,L-谷氨酰胺,胎牛血清或粒细胞巨噬细胞集落刺激因子(GM)的培养基中培养-CSF)或与白介素(IL)-4结合使用。细胞接受三种不同剂量的LPS和组胺,以及三种不同剂量的去甲乙氧基氯雷他定(DCL)。我们分析了上清液中的各种细胞因子。通过流式细胞术检查DO11.10小鼠的脾细胞,包括标记和分选CD4 + T细胞,以及DC和T细胞与卵清蛋白(OVA)323-339肽的共培养。组胺或组胺加DCL不会影响II型主要组织相容性复合物CD11c,CD11b,CD86和CD80的表达。但是,GM-CSF增加了除CD80外所有标记的表达。组胺可增加GM-CSF + IL-4培养细胞中干扰素-γ的产生;它也增强了IL-10的产生,但在没有DCL的LPS刺激的DC中抑制了IL-12的产生。西咪替丁抑制LPS处理的DC中IL-10的产生并恢复IL-12的分泌。 LPS增加IL-10并降低IL-12水平。 GM-CSF + IL-4生成的DC对DO11.10 T细胞增殖的刺激作用强于GM-CSF生成的DC。共培养2天后,GM-CSF + IL-4-诱导型共刺激素配体表达高于GM-CSF产生的DC组,但4天后降低。用GM-CSF产生的骨髓DC中IL-13的产生要高于用GM-CSF + IL-4产生的DC。 OVA脉冲DC和OVA加DCL DC显示IL-12水平升高。 OVA加LPS可增加IL-10和干扰素-α。尽管组胺或组胺受体1拮抗剂不影响DC LPS驱动的成熟,但它们影响细胞因子的产生。 LPS和GM-CSF影响了表面标志物的表达和细胞因子的产生。

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