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首页> 外文期刊>Brain research >Early events of the inflammatory reaction induced in rat brain by lipopolysaccharide intracerebral injection: relative contribution of peripheral monocytes and activated microglia.
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Early events of the inflammatory reaction induced in rat brain by lipopolysaccharide intracerebral injection: relative contribution of peripheral monocytes and activated microglia.

机译:脂多糖脑内注射在大鼠脑中诱发炎症反应的早期事件:外周单核细胞和活化的小胶质细胞的相对贡献。

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摘要

We have previously demonstrated that lipopolysaccharide (LPS) intracerebral injection induced only minimal inflammatory reaction in rat brain, apart from an increased number of 'brain macrophages' observed 24 h after LPS administration [Montero-Menei et al., Brain Res., 653 (1994) 101-111]. However, the nature of these 'brain macrophages' in the inflammatory response is still unclear. The present study focused on the early time-points (from 5 h to 24 h) after LPS injection or stab-lesion, and was aimed at the identification of the peripheral (monocytes) or parenchymal (microglia) origin of these 'brain macrophages'. OX42- and ED1-labeling did not clearly discriminate between monocytes/macrophages and reactive microglia, both cell types being immunoreactive. In other experiments, rats were made aplasic by irradiation prior to lesioning. These experiments clearly demonstrated that LPS induces an intense monocyte recruitment and, to a lesser extent, microglial activation since about 80% of the cells present 24 h after LPS injection consisted of recruited monocytes not observed in aplasic rats. Interestingly, our data show that LPS exerts a sequential dual action by first inhibiting the monocyte recruitment observed 5 h after stab lesion and then enhancing it at 15 h and 24 h after injection. A possible involvement of cytokines, chemokines and adhesion molecules in the mechanisms occurring in the early events of brain inflammatory reaction is discussed.
机译:先前我们已经证明,脂多糖(LPS)脑内注射在大鼠脑中仅引起最小的炎症反应,除了在LPS给药后24小时观察到的“脑巨噬细胞”数量增加外[Montero-Menei等,Brain Res。,653( 1994)101-111]。但是,这些“脑巨噬细胞”在炎症反应中的性质仍不清楚。本研究的重点是注射LPS或刺伤后的早期时间点(从5h到24h),旨在鉴定这些“脑巨噬细胞”的外周(单核细胞)或实质(小胶质细胞)起源。 。 OX42和ED1标记不能清楚地区分单核细胞/巨噬细胞和反应性小胶质细胞,两种细胞类型均为免疫反应性。在其他实验中,在损伤之前通过辐射使大鼠发育不全。这些实验清楚地表明,LPS诱导强烈的单核细胞募集,并在较小程度上诱导小胶质细胞活化,因为在LPS注射后24小时内约有80%的细胞由在发育不良大鼠中未观察到的募集的单核细胞组成。有趣的是,我们的数据表明,LPS通过先抑制刺伤后5 h观察到的单核细胞募集,然后在注射后15 h和24 h增强单核细胞募集而发挥顺序性双重作用。讨论了细胞因子,趋化因子和粘附分子可能参与的脑炎性反应的早期事件中发生的机制。

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