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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >TNF alpha and IL-1beta mediate intercellular adhesion molecule-1 induction via microglia-astrocyte interaction in CNS radiation injury.
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TNF alpha and IL-1beta mediate intercellular adhesion molecule-1 induction via microglia-astrocyte interaction in CNS radiation injury.

机译:TNFα和IL-1β通过中枢神经系统放射损伤中的小胶质细胞-星形胶质细胞相互作用介导细胞间粘附分子1诱导。

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摘要

Radiation injury to the central nervous system (CNS) results in glial activation accompanied by expression of pro-inflammatory cytokines and adhesion molecules. In this study we demonstrate intercellular adhesion molecule-1 (ICAM-1) induction in the irradiated mouse brain at the mRNA and protein levels. Immunocytochemical analysis revealed that ICAM-1 protein was primarily expressed in endothelial cells and microglia. In vitro, ionizing radiation significantly induces TNF alpha, IL-1beta and ICAM-1 mRNA in primary microglia cultures. Interestingly, although ionizing radiation activated primary astrocyte cultures, it did not induce ICAM-1 expression. However, exposure of astrocytes to conditioned medium collected from irradiated microglia resulted in ICAM-1 induction, which was abrogated when the conditioned medium was pre-incubated with neutralizing antibodies raised against murine TNF alpha and IL-1beta. These results indicate that pro-inflammatory cytokines may be necessary for ICAM-1 expression in astrocytes in CNS radiation injury.
机译:中枢神经系统(CNS)的放射损伤会导致神经胶质活化,并伴有促炎性细胞因子和粘附分子的表达。在这项研究中,我们证明了mRNA和蛋白质水平在辐照小鼠大脑中的细胞间粘附分子1(ICAM-1)诱导。免疫细胞化学分析显示,ICAM-1蛋白主要在内皮细胞和小胶质细胞中表达。在体外,电离辐射在原发性小胶质细胞培养物中显着诱导TNFα,IL-1beta和ICAM-1 mRNA。有趣的是,尽管电离辐射激活了原代星形胶质细胞培养,但它并未诱导ICAM-1表达。但是,星形胶质细胞暴露于从辐照的小胶质细胞收集的条件培养基会导致ICAM-1诱导,当条件培养基与针对鼠TNFα和IL-1beta产生的中和抗体一起预孵育时,ICAM-1诱导被废除。这些结果表明促炎细胞因子可能是中枢神经系统放射损伤中星形胶质细胞中ICAM-1表达的必要条件。

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