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Activation of microglial cells by the CD40 pathway: relevance to multiple sclerosis.

机译:CD40途径激活的小胶质细胞:与多发性硬化症相关。

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摘要

It is well known that microglial cells perform a key role in mediating inflammatory processes, which are associated with neurodegenerative diseases such as multiple sclerosis (MS). In this study, we report that CD40 expression on microglia is greatly enhanced by a low dose (10 U/ml) of IFN-gamma. We also find that ligation of microglial CD40 by CD40L triggers a significant production of TNF-alpha. Activation of microglia by ligation of CD40 in the presence of IFN-gamma results in cultured cortical neuronal injury, which is markedly attenuated by blockade of the CD40 pathway or neutralization of TNF-alpha. Finally, we find significant levels of IFN-gamma and TNF-alpha in the medium of co-cultured activated CD4+ T cells and microglial cells, showing that microglia can supply the CD40 receptor to activated CD4+ T cells and suggesting that this cellular interaction is a key event in MS pathophysiology.
机译:众所周知,小胶质细胞在介导与神经退行性疾病如多发性硬化症(MS)有关的炎性过程中起关键作用。在这项研究中,我们报告说小剂量(10 U / ml)的IFN-γ可大大增强CD40在小胶质细胞上的表达。我们还发现,CD40L连接小胶质细胞CD40会触发TNF-α的大量产生。在存在IFN-γ的情况下,通过CD40的连接来激活小胶质细胞会导致培养的皮质神经元损伤,这种损伤会因CD40途径的阻断或TNF-α的中和而明显减弱。最后,我们在共培养的活化CD4 + T细胞和小胶质细胞的培养基中发现了显着水平的IFN-γ和TNF-α,这表明小胶质细胞可以向活化CD4 + T细胞提供CD40受体,这表明这种细胞相互作用是一种MS病理生理学中的关键事件。

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