首页> 美国卫生研究院文献>Oxidative Medicine and Cellular Longevity >Milk Fat Globule-Epidermal Growth Factor-Factor 8 Reverses Lipopolysaccharide-Induced Microglial Oxidative Stress
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Milk Fat Globule-Epidermal Growth Factor-Factor 8 Reverses Lipopolysaccharide-Induced Microglial Oxidative Stress

机译:牛奶脂肪球-表皮生长因子因子8逆转脂多糖诱导的小胶质细胞氧化应激。

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摘要

Oxidative stress plays an important role in various neurological disorders. Milk fat globule-epidermal growth factor-factor 8 (MFG-E8) is a regulatory protein for microglia. However, its involvement in microglial oxidative stress has not been established. In this study, we observed microglial oxidative stress in response to lipopolysaccharide (LPS) both in vitro and in vivo. LPS induced significant elevation of TNF-α, IL-6, MDA, and ROS and reduction of GSH and SOD in the mouse brains and primary microglia, which were reversed by MFG-E8 pretreatment. MFG-E8 induced the expression of Nrf-2 and HO-1 that was reduced by LPS incubation. Moreover, LPS-increased Keap-1 expression was reversed by MFG-E8. But the above tendencies were not seen when MFG-E8 was applied alone. The current study established the involvement of MFG-E8 in antioxidant effects during neuroinflammation. It may achieve the effects through the regulation of Keap-1/Nrf-2/HO-1 pathways.
机译:氧化应激在各种神经系统疾病中起重要作用。乳脂球-表皮生长因子8(MFG-E8)是小胶质细胞的调节蛋白。然而,尚未确定其参与小胶质细胞氧化应激。在这项研究中,我们观察到在体外和体内对脂多糖(LPS)响应的小胶质细胞氧化应激。 LPS诱导小鼠脑和原发性小胶质细胞中TNF-α,IL-6,MDA和ROS的显着升高以及GSH和SOD的降低,而MFG-E8预处理则可以逆转。 MFG-E8诱导了Nrf-2和HO-1的表达,LPS孵育降低了该表达。此外,MFG-E8逆转了LPS升高的Keap-1表达。但是,当单独使用MFG-E8时,看不到上述趋势。目前的研究确定了MFG-E8参与神经炎症过程中的抗氧化作用。它可能通过调节Keap-1 / Nrf-2 / HO-1途径达到效果。

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