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外周血单个核细胞对培养的口腔鳞状细胞癌条件培养基的反应。

Response of peripheral blood mononuclear cells to conditioned medium from cultured oral squamous cell carcinomas.

机构信息

School of Dentistry, Universidade Nove de Julho, São Paulo, SP, Brazil.

出版信息

Braz Oral Res. 2011 Sep-Oct;25(5):414-20. doi: 10.1590/s1806-83242011000500007.

Abstract

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.

摘要

本研究旨在探讨头颈部鳞状细胞癌(HNSCC)细胞系 KB、KB16 和 HEP 分泌的肿瘤因子对人外周血单个核细胞(PBMC)分泌各种细胞因子的能力。从 6 名健康志愿者采集的血液样本中分离 PBMC,在存在 50%经细胞系预处理后的条件培养基(无刺激物或有植物血凝素(PHA)或脂多糖(LPS)刺激物)的情况下,将这些细胞孵育 6、24、48 或 72 小时。然后,将每份上清液的等分试样用于通过酶联免疫吸附测定(ELISA)检测 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、方差分析 followed by Tukey 检验和 Pearson 相关性检验分析收集的数据。用 KB16 条件培养基培养的 PBMC 产生的 IFN-Γ 水平最高。在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了 VEGF,并且在对照和 KB 或 KB16 条件培养基之间观察到 VEGF 水平的显著差异。所有 PBMC 组在接受条件培养基 6 小时内均分泌 TNF-α,并且这些水平增加到 24 小时时间点,之后 TNF-α 水平稳定。相比之下,没有任何上清液样品含有可检测水平的 IL-4。综合这些数据表明,新鲜人 PBMC 与肿瘤细胞的条件培养基直接接触诱导 PBMC 分泌 TNF-α和 VEGF,这代表了初始的血管生成反应。

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