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成纤维细胞和T细胞条件培养基可诱导树突状细胞成熟并促进辅助性T细胞免疫反应。

Fibroblast and T cells conditioned media induce maturation dendritic cell and promote T helper immune response.

作者信息

Asadi Masoumeh, Farokhi Farah, Delirezh Nowruz, Ganji Bakhsh Meysam, Nejati Vahid, Golami Keykavos

机构信息

Department of Biology and Embryology, Faculty of Science, Urmia University, Urmia, Iran;

Department of Immunology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

出版信息

Vet Res Forum. 2012 Spring;3(2):111-8.

Abstract

Dendritic cells (DCs) induce pathogen-specific T cell responses. We comprehensively studied the effects of addition of maturation stimulus, fibroblasts (fibroblast conditioned medium), PHA activated T cells (T cell conditioned medium), and mixture of fibroblast & PHA activated T cells (FCM-TCCM) conditioned media on maturation of DCs. Monocytes were cultured with GM-CSF and IL-4 for five days. Maturation factors included MCM and TNF-α as control group. FCM and TCCM, or FCM-TCCM supernatant were considered as the treatment group. Tumor antigens were added at day five. Matured DCs were harvested at day seven. Phenotypic and functional analyses were carried out using anti (CD14, CD80, CD86, CD83 and HLA-DR) monoclonal antibodies. Phagocytic activity, mixed lymphocyte reaction (MLR) and cytokine production were also evaluated. At the end of culturing period, significantly fully matured DCs with large amount cytoplasm and copious dendritic projections were found in the presence of MCM, TNF-α with or without FCM, TCCM, FCM as well as TCCM. Flow cytometric analysis revealed that expression of CD14 decreased in particular in treated DCs, at the 5(th) day and expression of CD80, CD86 and HLA-DR was higher when FCM, TCCM, FCM plus TCCM were added to maturation factor. This study demonstrated that DCs matured with these methods had optimum function in comparison with either factor alone.

摘要

树突状细胞(DCs)可诱导病原体特异性T细胞反应。我们全面研究了添加成熟刺激剂、成纤维细胞(成纤维细胞条件培养基)、PHA激活的T细胞(T细胞条件培养基)以及成纤维细胞与PHA激活的T细胞混合物(FCM-TCCM)条件培养基对DCs成熟的影响。单核细胞用GM-CSF和IL-4培养5天。成熟因子包括MCM和TNF-α作为对照组。FCM和TCCM,或FCM-TCCM上清液作为治疗组。在第5天添加肿瘤抗原。在第7天收获成熟的DCs。使用抗(CD14、CD80、CD86、CD83和HLA-DR)单克隆抗体进行表型和功能分析。还评估了吞噬活性、混合淋巴细胞反应(MLR)和细胞因子产生。在培养期结束时,在存在MCM、TNF-α以及有或无FCM、TCCM、FCM和TCCM的情况下,发现了大量具有丰富细胞质和大量树突状突起的显著完全成熟的DCs。流式细胞术分析显示,在第5天,特别是在处理过的DCs中,CD14的表达下降,当将FCM、TCCM、FCM加TCCM添加到成熟因子中时,CD80、CD86和HLA-DR的表达更高。本研究表明,与单独使用任何一种因子相比,用这些方法成熟的DCs具有最佳功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8a7/4312805/bd88ad0bc804/vrf-3-111-g001.jpg

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