首页|大黄酸对脂多糖诱导小胶质细胞极化表型及相关炎症因子的影响

大黄酸对脂多糖诱导小胶质细胞极化表型及相关炎症因子的影响

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目的 研究大黄酸对脂多糖(LPS)诱导小胶质细胞极化表型及相关炎症因子的影响.方法 体外培养小胶质细胞,分为空白组,LPS组,大黄酸低、中、高剂量组.空白组常规培养,其余四组加入1 μg/ml LPS干预诱导,LPS组给予正常培养基,大黄酸低、中、高剂量组分别给予1、10、20 μmol/L大黄酸.使用倒置显微镜观察小胶质细胞形态;CCK-8法检测小胶质细胞活性;流式细胞术检测小胶质细胞中CD86+(M1型)和CD206+(M2型)的比例;采用酶联免疫吸附试验检测细胞上清液中白细胞介素(IL)-1β、IL-6及肿瘤坏死因子-α(TNF-α)的含量;采用试剂盒测定诱导型一氧化氮合酶(iNOS)活性.结果 不同浓度大黄酸对LPS诱导的小胶质细胞形态及细胞增殖无明显影响.与空白组比较,LPS组CD86+表达量升高,CD206+表达量降低(P<0.05);与LPS组比较,大黄酸中、高剂量组CD86+表达量降低,CD206+表达量升高(P<0.05);与大黄酸低剂量组比较,大黄酸中、高剂量组CD86+表达量降低,CD206+表达量升高(P<0.05).与空白组比较,LPS组中IL-1β、IL-6、TNF-α表达量升高(P<0.05).与LPS组比较,大黄酸中、高剂量组IL-1、IL-6、TNF-α表达量降低(P<0.05).与大黄酸低剂量组比较,大黄酸中、高剂量组IL-1、IL-6、TNF-α低表达量降低(P<0.05).与空白组比较,LPS组iNOS表达量升高(P<0.05).与LPS组比较,大黄酸低、中及高剂量组iNOS表达量降低(P<0.05).结论 大黄酸可使LPS诱导的小胶质细胞极化表型由M1型向M2型转化,继而减少相关炎症因子的释放,以发挥其抗炎作用.
Effect of rhein on lipopolysaccharide induced polarization phenotype of microglia and related inflammatory factors
Objective To investigate the effect of rhein on lipopolysaccharide(LPS)induced polarization phenotype of microglia and related inflammatory factors.Methods Microglia were cultured in vitro and divided into blank group,LPS group,low,medium,and high dose rhein group,blank group was cultured routinely,and the remaining four groups were induced by the addition of 1 μg/ml LPS intervention,normal medium was given to the LPS group,and 1,10,and 20 μmol/L of rhein was given to the low,medium,and high dose rhein group,respectively.Microglia morphology was observed by inverted microscope;microglia activity was detected by CCK-8;the ratio of CD86+(M1-type)and CD206+(M2-type)in microglia was detected by flow cytometry;and the content of interleukin(IL)-1 β,IL-6,and tumor necrosis factor-α(TNF-α)in the cellular supernatant was detected by enzyme linked immunosorbent assay,and inducible nitric oxide synthase(iNOS)activity was determined by kit.Results Rhein at different concentrations had no significant effect on the morphology and proliferation of LPS-induced microglia.Compared with blank group,CD86+expression was increased and CD206+expression was decreased in LPS group(P<0.05).Compared with LPS group,the expression of CD86+in medium and high dose rhein groups was decreased,and the expression of CD206+was increased(P<0.05).Compared with low dose rhein group,CD86+expression decreased and CD206+expression increased in medium and high dose rhein groups(P<0.05).Compared with blank group,the expression of IL-1 β,IL-6,and TNF-αin LPS group were increased(P<0.05).Compared with LPS group,the expressions of IL-1,IL-6,and TNF-α in medium and high dose rhein groups were decreased(P<0.05).Compared with low dose rhein group,the expressions of IL-1,IL-6,and TNF-α in medium and high dose rhein groups were decreased(P<0.05).Compared with blank group,iNOS expression in LPS group was increased(P<0.05).Compared with LPS group,iNOS expression in low,medium,and high dose rhein groups was decreased(P<0.05).Conclusion Rhein converts the LPS-induced microglia polarization phenotype from M1-type to M2-type,which subsequently reduces the release of relevant inflammatory factors to exert its anti-inflammatory effects.

RheinMicrogliaPolarization phenotypeInflammatory factor

李倩、陈臣、胡燕、谢晓林、刘涛

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新疆医科大学第四临床医学院,新疆乌鲁木齐 830000

大黄酸 小胶质细胞 极化表型 炎症因子

新疆维吾尔自治区自然科学基金杰出青年科学基金

2022D01E79

2024

中国医药导报
中国医学科学院

中国医药导报

CSTPCD
影响因子:1.759
ISSN:1673-7210
年,卷(期):2024.21(11)
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