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Down-Regulation of CD14 Transcripts in Human Glioblastoma Cell Line U87 MG

机译:人胶质母细胞瘤细胞系U87 MG CD14转录本的下调。

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Background: Pattern recognition receptors (PRRs) are the main sensors of pathogen and danger signals in innate immunity of which Toll Like Receptors (TLRs) are the most studied ones. The contribution of PRRs in cerebral inflammation induced by microbial infection, tissue damage and cancer has not extensively been addressed so far. Glioma is the most common tumor of the central nervous system and glioblastomas are the most common and most malignant primary brain tumors. Objective: The objectives of the present study were to investigate the expression of several PRRs including TLR2, TLR4, MyD88 and CD14 transcripts in human glioblastoma cell line U87 MG and compare their expression level with peripheral blood mononuclear cells (PBMC) obtained from healthy individuals. Methods: Touchdown PCR (TD-PCR) and Realtime quantitative PCR (qPCR) were applied to detect and quantify the expression level of TLR2, TLR4, MyD88 and CD14 transcript in U87 MG cell line and (PBMC) of healthy individuals. Results: According to our results, human glioblastoma cell line U87 MG expresses TLR2, TLR4, MyD88 and CD14 transcripts in TD-PCR. Moreover, the quantification of the expression of these genes revealed a highly significant downregulation of CD14 and a slight up-regulation of TLR2 transcripts as compared to PBMC of healthy individuals. Conclusion: The lower expression level of CD14 in human glioblastoma cell line, might have a potential implication for CD14 mediated cerebral pathology.
机译:背景:模式识别受体(PRR)是先天免疫中病原体和危险信号的主要传感器,其中Toll样受体(TLR)是研究最多的传感器。迄今为止,PRRs在由微生物感染,组织损伤和癌症引起的脑部炎症中的作用尚未得到广泛解决。胶质瘤是中枢神经系统最常见的肿瘤,胶质母细胞瘤是最常见也是最恶性的原发性脑肿瘤。目的:本研究的目的是研究人胶质母细胞瘤细胞系U87 MG中TLR2,TLR4,MyD88和CD14转录本等几种PRR的表达,并将其与健康人外周血单个核细胞(PBMC)的表达水平进行比较。方法:应用落地PCR(TD-PCR)和实时定量PCR(qPCR)检测和定量检测健康个体U87 MG细胞系和PBMC中TLR2,TLR4,MyD88和CD14转录本的表达水平。结果:根据我们的结果,人胶质母细胞瘤细胞系U87 MG在TD-PCR中表达TLR2,TLR4,MyD88和CD14转录本。而且,与健康个体的PBMC相比,这些基因表达的定量揭示了CD14的高度显着下调和TLR2转录本的轻微上调。结论:人胶质母细胞瘤细胞中CD14的较低表达水平,可能对CD14介导的脑病理学有潜在的影响。

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