Wu Xing, Yu Tengbo, Xu Hongyan, Sun Xiuming, Kou Dewei, Li Liping
Department of Pain Clinic, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Department of Bone Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Exp Ther Med. 2018 Feb;15(2):2015-2019. doi: 10.3892/etm.2017.5596. Epub 2017 Dec 5.
This study investigated the effects of different concentrations of oxygen exposure on the morphology and function of N9 microglia and analyzed its mechanisms. N9 microglia were cultured under the condition of high (95% O and 5% CO), normal (95% air and 5% CO) and low oxygen (95% CO and 5% O) concentrations. The cell morphologies were observed under inverted phase contrast microscope after 24 h. Flow cytometry was applied to detect cell survival and apoptotic rate. The mRNA and protein expression levels of interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were detected by reverse transcription-polymerase chain reaction (RT-PCR) and western blot analysis, respectively. The results showed that, N9 microglial apoptotic rates in hyperoxia and hypoxia conditions were significantly higher than those in the normal group (P<0.05) and the apoptosis rate in the hypoxia group was higher than that in the hyperoxia group (P<0.05). The mRNA and protein expression levels of IL-1β and TNF-α in the hyperoxia and hypoxia groups were significantly higher than those in the normal group (P<0.05) and the mRNA and protein expression levels in hypoxia group were higher than those in the hyperoxia group (P<0.05). Therefore, N9 microglia cultured under hyperoxia and hypoxia conditions can be activated, enhancing pro-inflammatory response and inducing cell apoptosis. The mechanism may be that the secretion of neurotoxic factors IL-1β and TNF-α is involved in these responses.
本研究探讨了不同浓度氧暴露对N9小胶质细胞形态和功能的影响,并分析其机制。将N9小胶质细胞分别在高氧(95%O₂和5%CO₂)、正常(95%空气和5%CO₂)和低氧(95%CO₂和5%O₂)浓度条件下培养。24小时后在倒置相差显微镜下观察细胞形态。应用流式细胞术检测细胞存活率和凋亡率。分别通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析检测白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的mRNA和蛋白表达水平。结果显示,高氧和低氧条件下N9小胶质细胞凋亡率显著高于正常组(P<0.05),且低氧组凋亡率高于高氧组(P<0.05)。高氧和低氧组IL-1β和TNF-α的mRNA和蛋白表达水平显著高于正常组(P<0.05),且低氧组mRNA和蛋白表达水平高于高氧组(P<0.05)。因此,在高氧和低氧条件下培养的N9小胶质细胞可被激活,增强促炎反应并诱导细胞凋亡。其机制可能是神经毒性因子IL-1β和TNF-α的分泌参与了这些反应。