木妮然·吐尔逊江,帕丽达·阿不力孜,丛媛媛,依明·尕哈甫,米仁沙·牙库甫.阿里红多糖对Aβ25-35诱导的小胶质细胞炎症 反应的影响[J].食品安全质量检测学报,2018,9(22):5943-5948
阿里红多糖对Aβ25-35诱导的小胶质细胞炎症 反应的影响
Effects of Fomes officinais Ames polysaccharides on Aβ25-35 induced inflammatory response of microglia
投稿时间:2018-09-30  修订日期:2018-11-14
DOI:
中文关键词:  阿尔茨海默病  小胶质细胞  Aβ25-35蛋白  阿里红粗多糖
英文关键词:alzheimer's disease  microglial cell  Aβ25-35  Fomes officinais Ames polysaccharides
基金项目:新疆维吾尔自治区科技援疆项目(201591190)、国家自然科学基金项目(81760755)
作者单位
木妮然·吐尔逊江 新疆医科大学 
帕丽达·阿不力孜 新疆医科大学 
丛媛媛 新疆医科大学 
依明·尕哈甫 新疆医科大学 
米仁沙·牙库甫 新疆医科大学 
AuthorInstitution
munirantuerxunjiang xinjiangyikedaxue 
palidaabulizi xinjiangyikedaxue 
CONG Yuan-Yuan College of Pharmacy, Xinjiang Medical University 
yiminggahafu xinjiangyikedaxue 
mirenshayakufu xinjiangyikedaxue 
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中文摘要:
      目的 探讨阿里红多糖(Fomes Officinals polysaccharide, FOPS)及多糖组分(FOP-a)对Aβ25-35诱导的BV-2小胶质细胞炎症反应的抑制作用。方法 采用Aβ25-35诱导BV-2小胶质细胞活化建立阿尔茨海默病(alzheimer disease, AD)炎症细胞模型, 将BV-2细胞分为空白组、炎症模型组(加40 μg/mLAβ25-35)、不同浓度的FOPS及FOP-a干预组(6.25、12.5、25 μg/mL)。在倒置显微镜下观察细胞形态, 酶联免疫法(enzyme linked immunosorbent assay, ELISA)检测细胞上清中IL-6及单核细胞趋化因子(MCP-1)分泌量; Western blotting法测定NF-κB及IκBα蛋白表达量。结果 Aβ25-35诱导后小胶质细胞出现阿米巴样状态, 通过不同剂量FOPS及FOP-a干预, 能明显改善Aβ25-35对BV-2细胞造成的损伤, 与模型组比较, FOPS及FOP-a可提高细胞存活率。ELISA实验结果显示与空白组比较, 模型组IL-6及MCP-1的分泌量增加, 与模型组比较, FOPS及FOP-a均能减少IL-6及MCP-1的分泌量, 差异有统计学意义(P<0.05)。Western blotting结果显示, 与空白组比较, 模型组细胞上调NF-κB-p65蛋白表达、减少IκBα的蛋白表达, 与模型组比较FOPS及FOP-a均能减少NF-κB-p65和上调IκBα的蛋白表达。结论 阿里红粗多糖及多糖组分均能减轻Aβ25-35诱导的BV-2细胞的炎症作用, 其中FOPS浓度为12.5 μg/mL、FOP-a浓度为25 μg/mL时效果最佳。
英文摘要:
      Objective To investigate the inhibitory effects of Fomes officinais Ames polysaccharides(FOPS) and polysaccharides components (FOP-a) on the inflammatory response in BV-2 microglial cells induced by Aβ25-35. Methods Alzheimer's disease (AD) inflammatory cell model was established by induction of BV-2 microglia activation by Aβ25-35.BV-2 cells were divided into blank group, inflammatory model group (40 μg/mL Aβ25-35), different concentrations of FOPS and FOP-a intervention group (6.25, 12.5, 25 μg/mL). The morphology of the cells was observed under an inverted microscope, the secretion of IL-6 and monocyte chemotactic factor (MCP-1) in the supernatant of the cells was detected by enzyme linked immunosorbent assay (ELISA), and NF-κB and IκBα protein expression were detected by Western blotting. Results After Aβ25-35 induction, microglia showed amoebic-like state. Different doses of FOPS and FOP-a could significantly improve the damage of BV-2 cells induced by Aβ25-35. Compared with the model group, FOPS and FOP-a could increase cell survival rate. The results of ELISA showed that the secretion of IL-6 and MCP-1 increased in the model group compared with the blank group; compared with the model group, both FOPS and FOP-a could reduce the secretion of IL-6 and MCP-1, and the difference was statistically significant (P<0.05).Western blotting results showed that compared with the blank group, the model group could up-regulate the expression of NF-κB-p65 protein and decrease the protein expression of IκBα. Both FOPS and FOP-a could reduce NF-κB-p65 and up-regulate IκBα protein expression compared with the model group. Conclusion Polysaccharides components FOPS and FOP-a from Fomes officinais Ames can alleviate the inflammatory effects of Aβ25-35-induced BV-2 cells, and the best effect is when the FOPS concentration is 12.5 μg/mL and the FOP-a concentration is 25 μg/mL.
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