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作 者:房明[1] 汪涛[1] 王欣[1] 王新文[1] 王勤涛[1]
机构地区:[1]第四军医大学口腔医学院,陕西西安710032
出 处:《牙体牙髓牙周病学杂志》2012年第4期200-202,226,共4页Chinese Journal of Conservative Dentistry
基 金:十一五国家科技支撑计划课题(2007BAI18B02)
摘 要:目的:研究比较在体外高糖、糖基化终产物(advanced glycation end of products,AGEs)刺激环境下对人牙周膜细胞(hPDLFs)增殖能力和NF-κB mRNA表达的影响。方法:选取因正畸治疗而拔除的前磨牙体外分离培养人牙周膜细胞,根据不同的刺激环境分为阴性对照组(5.5 mmol/L葡萄糖)、高糖组(25 mmol/L葡萄糖)、AGEs组(100μg/mL AGEs)3组。培养12、24、36 h,3个时间点,使用Real Time PCR检测各组NF-κBmRNA的表达差异情况;流式细胞仪检测培养hPDLFs 36 h时细胞增殖差异情况。结果:在培养12、24、36 h,高糖组和AGEs组NF-κB mRNA的表达均高于阴性对照组(P<0.05),其中AGEs组最高,与高糖组相比,24、36 h时均有统计学差异(P<0.05);培养36 h AGEs组hPDLFs增殖能力明显低于阴性对照组和高糖组(P<0.05);高糖组与阴性对照组相比无统计学差异(P>0.05)。结论:AGEs能够显著的抑制hPDLFs增殖,并上调NF-κB的表达呈时间依赖性。AIM: To study the influence of high glucose environment and advanced glycation end products(AGEs) on the proliferation and NF-κB mRNA expression of human periodontal ligament fibroblasts(hPDLFs) in vitro.METHODS: The hPDLFs were isolated from premolars extracted for orthodontic purpose.Cells were divided into 3 groups: negative control group(5.5mmol/L glucose),high glucose group(25mmol/L glucose) and AGEs group(100μg/mL AGEs).After 12,24 and 36 h of culture,real time PCR was used to assess the NF-κB mRNA level.After 36h of culture,flow cytometry was applied to test the proliferation of 3 groups.RESULTS: At 12 h,24 h and 36 h,the NF-κB mRNA expression was elevated in AGEs group and high glucose group(P〈0.05).AGEs group exhibited higher NF-κb mRNA expression than high glucose group at 24 h and 36 h(P〈0.05).After 36 h of culture,the proliferation of hPDLFs in AGEs group was inhibited compared to the other two groups(P〈0.05).There was no statistical significance between high glucose group and negative control group(P〈0.05).CONCLUSION: AGEs can strongly inhibit the proliferation of hPDLFs and enhance their NF-κB expression in a time dependent manner.
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