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作 者:林俊卿 黄蔷如 王弼思 吴坷坷 谭宇蓉 彭程[3] 邬国军 LIN Jun-qing;HUANG Qiang-ru;WANG Bi-si;WU Ke-ke;TAN Yu-rong;PENG Cheng;WU Guo-jun(Xiangya School of Medicine, Central South University, Changsha 410016, China;Department of Microbiology, School of Basic Medical Sciences, Central South University;Burns and Plastic Surgery, the Third Xiangya Hospital affiliated with Central South University)
机构地区:[1]中南大学湘雅医学院,湖南长沙410016 [2]中南大学基础医学院微生物学系 [3]中南大学湘雅三医院烧伤整形外科
出 处:《中国病原生物学杂志》2017年第12期1161-1164,共4页Journal of Pathogen Biology
基 金:中南大学创新创业基金项目(No.201510533319)
摘 要:目的研究槲皮素(quercetin)对人永生化上皮细胞(HaCat细胞)增殖及其非特异性免疫分子表达的影响。方法利用MTT法检测不同浓度槲皮素溶液作用对HaCat细胞增殖的影响,利用ELISA法检测在不同浓度槲皮素干预下的HaCat细胞培养上清液中β-防御素(β-DF)及谷胱甘肽过氧化物酶(GPX)的含量。结果 100μmol/L槲皮素对HaCat细胞的增殖有抑制作用,50μmol/L以下的槲皮素对HaCat细胞的增殖无明显影响。HaCat细胞经过不同浓度的槲皮素处理48、72h后,其细胞上清液中谷胱甘肽过氧化物酶的浓度与对照组比较差异有统计学意义(P<0.05),但β-防御素的表达在50.00μmol/L和25.00μmol/L槲皮素处理组上调。结论槲皮素具有增强细胞非特异免疫功能作用,其机制可能通过上调β-防御素的表达来实现。Objective To study the effect of quercetin on the proliferation of HaCat cells and the expression of nonspecific immunity molecules(glutathione peroxidase andβ-defensin).Methods The proliferation of HaCat cells after treatment with different concentrations of quercetin(100.00,50.00,25.00,12.50,6.25,and 0.00μmol/L)was detected using an MTT assay.The concentrations ofβ-defensin and glutathione peroxidase in HaCat cell culture supernatants treated with different concentrations of quercetin were detected with ELISA. Methods The proliferation of HaCat cells after treatment with different concentrations of quercetin(100.00,50.00,25.00,12.50,6.25,and 0.00μmol/L)was detected using an MTT assay.The concentrations ofβ-defensin and glutathione peroxidase in HaCat cell culture supernatants treated with different concentrations of quercetin were detected with ELISA. Results The proliferation of HaCat cells was significantly inhibited by 100μmol/L quercetin(compared to treatment with 0.00μmol/L quercetin;the t values was 9.84 12 hafter treatment with 100.00μmol/L quercetin,13.33 24 hafter treatment,11.34 48 hafter treatment,11.84 72 hafter treatment,and 14.88 96 hafter treatment,P〉0.05 for all).However,a concentration of quercetin less than 50μmol/L had no effect on HaCat cell proliferation(compared to treatment with 0.00μmol/L quercetin;the Fvalues were 2.02 12 hafter treatment with 50.00,25.00,12.50,or 6.25μmol/L quercetin,2.46 24 hafter treatment,0.59 48 hafter treatment,2.72 72 hafter treatment,and 2.75 96 hafter treatment(P〈0.05 for all).The concentration of glutathione peroxidase(GPX)in the cell culture supernatant 48 hand 72 hafter treatment with quercetin decreased markedly compared to that in the control group(the Fvalues were 24.53 and 5.78,respectively,P〈0.05 for both).Cells treated with 50.00,25.00,12.50,or 6.25μmol/L quercetin for 48 hhad a significantly lower concentration of GPX in the supernatant(14.29±0.58 pg/mL,14.11±0.26 pg/mL,16.21±0.76 pg/mL and 16.60±0
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