Ⅰ型鼠尾胶原三维培养模型对树突状细胞形态及分泌能力的影响  被引量:2

The Effects of T-dimensional Rat Tail Collagen Ⅰ Cultivation Model on Morphology and Cytokine Secretion Capacity of Dendritic Cells

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作  者:黄文竹 胡文慧 曾柱 

机构地区:[1]贵州医科大学生物与工程学院,贵州贵阳550004 [2]贵州医科大学生物与医学工程重点实验室,贵州贵阳550004

出  处:《贵州医科大学学报》2017年第9期993-997,1002,共6页Journal of Guizhou Medical University

基  金:国家自然科学基金(31260227;11162003;31771014;11762006);贵州省2011协同创新计划(2015-04);贵州省科技创新人才团队(2015-4021);教育部科学技术基金重点项目(210196);贵州省科技厅科技合作项目(LH-2016-7375);贵州医科大学博士启动基金(2014-024;2014-022)

摘  要:目的:通过构建Ⅰ型鼠尾胶原三维(3D)培养模型,探索细胞外力学微环境对DCs产生的影响。方法:取健康人外周血来源的CD14+单核细胞,利用重组人白介素-4(rh IL-4)和重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)共同诱导5 d,获得未成熟DCs(im DCs),再利用重组人干扰素-γ(rh IFN-γ)和脂多糖(LPS)诱导im DCs为成熟DCs(mDCs);再利用鼠尾肌腱提取Ⅰ型鼠尾胶原体外培养DCs;FITC-Annexin-V和碘化丙啶(PI)标记细胞,检测DCs的凋亡率;酶联免疫吸附测定法检测DC的白细胞介素-12(IL-12)、IL-18和IL-1β的分泌水平。结果:与对照组相比,3D力学环境处理后细胞形态发生改变,细胞早期凋亡率降低,IL-18和IL-1β的分泌能力发生下调(P<0.05)。结论:细胞外3D力学微环境能够调控DCs的免疫功能。Objective: To study the effects of extracellular mechanical microenvironment on dendriticcells (DCs) by establishing three-dimensional rat tail collagen I cultivation model. Methods: CD14+ peripheral blood mononuclear cells were induced to imDCs by recombinant human interleukin-4( rhIL- 4) and recombinant human granulocyte-macrophage colony-stimulating factor(rhGM-CSF) , and then induced to mDCs by recombinant human interferon γ(rhIFN-γ) and lipopolysaccharide (LPS) . Rat tail collagen I was extracted from rat tail tendon and then used to cultivate DCs in vitro. The cell apop- tosis were measured by FITC-Annexin-V and PI labeled cells. The cytokine production levels were measured by Elisa kit. Results: Compared with control group, the 3 D extracellular mechanical micro- environment could induce the morphological change, the ratio of early apoptosis were down-regulated, cytokine including IL-18 and IL-1β secretion capacity were down-regulated ( P 〈 0.05 ). Conclusions: The 3D extracellular mechanical microenvironment could regulate the immune function of DCs.

关 键 词:树突状细胞 Ⅰ型鼠尾胶原 三维培养模型 凋亡 白细胞介素 免疫功能 

分 类 号:R392.12[医药卫生—免疫学] Q63[医药卫生—基础医学]

 

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