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首页> 外文期刊>Brazilian Oral Research >Response of peripheral blood mononuclear cells to conditioned medium from cultured oral squamous cell carcinomas
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Response of peripheral blood mononuclear cells to conditioned medium from cultured oral squamous cell carcinomas

机译:口腔鳞状细胞癌对外周血单个核细胞对条件培养基的反应

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摘要

The current study investigated the capacity for tumor factors secreted by head and neck squamous cell carcinoma (HNSCC) cell lines, KB, KB16, and HEP, to induce the secretion of various cytokines from peripheral blood mononuclear cells (PBMCs). PBMCs were isolated from blood samples collected from six healthy volunteers and these cells were incubated for 6, 24, 48, or 72 hours in the presence of 50% conditioned medium collected from cultured cell lines pretreated with, or without, stimulants such as phytohemagglutinin (PHA) or lipopolysaccharides (LPS). Aliquots of each supernatant were then assayed for levels of IFN-Γ, vascular endothelial growth factor (VEGF), TNF-α, and IL-4 using enzyme linked immunosorbent assays (ELISAs). Data collected were analyzed using Student's t-test, an ANOVA test followed by Tukey's test, and tests of Pearson's Correlation. PBMCs cultured with KB16-conditioned medium produced the highest levels of IFN-Γ. VEGF was also detected in conditioned media collected from all of the squamous cell carcinoma (SCC) cell lines used, and a significant difference in VEGF levels between control and KB- or KB16-conditioned media was observed. TNF-α was secreted by all PBMC groups within 6 hours of receiving conditioned media, and these levels increased up to the 24 hour timepoint, after which levels of TNF-α stabilized. In contrast, none of the supernatant samples contained detectable levels of IL-4. In combination, these data suggest that direct contact between fresh human PBMCs and conditioned media from tumor cells induces the secretion of TNF-α and VEGF by PBMCs, and this represents an initial angiogenic response.
机译:当前的研究调查了头颈鳞状细胞癌(HNSCC)细胞系KB,KB16和HEP分泌的肿瘤因子诱导外周血单核细胞(PBMC)分泌多种细胞因子的能力。从六名健康志愿者的血液样本中分离出PBMC,并将这些细胞在50%条件培养基中孵育6、24、48或72小时,条件培养基是从培养的细胞系中收集的,这些细胞系经过或未经过刺激物如植物血凝素( PHA)或脂多糖(LPS)。然后使用酶联免疫吸附测定法(ELISA)测定各上清液的等分试样的IFN-γ,血管内皮生长因子(VEGF),TNF-α和IL-4的水平。使用学生t检验,ANOVA检验,Tukey检验以及Pearson关联检验对收集的数据进行分析。用KB16条件培养基培养的PBMC产生最高水平的IFN-Γ。在从所有使用的鳞状细胞癌(SCC)细胞系收集的条件培养基中也检测到VEGF,并且在对照和KB-或KB16条件培养基之间观察到VEGF水平的显着差异。接受条件培养基后6个小时内,所有PBMC组均分泌TNF-α,并且这些水平一直上升到24小时,此后TNF-α的水平稳定下来。相反,所有上清液样品均不含可检测水平的IL-4。综合起来,这些数据表明新鲜的人PBMC与肿瘤细胞的条件培养基之间的直接接触诱导了PBMC分泌TNF-α和VEGF,这代表了初始的血管生成反应。

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