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作 者:胡超 祝金浩 殷园 贺小涛 李璇 张曦予 陈发明(指导)
机构地区:[1]第四军医大学口腔医院牙周科,军事口腔医学国家重点实验室,口腔疾病国家临床医学中心,陕西省口腔生物工程技术研究中心,陕西西安710032 [2]解放军77626部队医院,西藏拉萨851400 [3]不详
出 处:《牙体牙髓牙周病学杂志》2017年第5期254-260,共7页Chinese Journal of Conservative Dentistry
基 金:国家自然科学基金(81500853)
摘 要:目的:观察白藜芦醇预处理能否衰使老牙周膜干细胞(Aged-PDLSCs)的增殖潜能和克隆形成能力得到增强。方法:将体外分离培养的中老年个体来源PDLSCs随机分为常规培养组、白藜芦醇预处理组、尼克酰胺预处理组;各组经相应处理后,采用MTT法检测其增殖潜能,结晶紫染色检测其克隆形成能力,RT-PCR和Western Blot检测其细胞中SIRT1和P53基因及蛋白的表达水平。结果:Aged-PDLSCs经白藜芦醇预处理后增殖潜能和克隆形成能力均得到了显著提高,而经尼克酰胺预处理后,其增殖潜能和克隆形成能力均明显降低;分别与常规培养组相比,差异均有统计学意义(P<0.05)。此外,白藜芦醇预处理还可显著提高Aged-PDLSCs中SIRT1活性(P<0.05),显著降低了P53的表达水平(P<0.05)。结论:白藜芦醇能够增强Aged-PDLSCs的克隆形成能力和增殖潜能,其作用可能是通过提高SIRT1的表达水平而实现的。AIM To investigate whether resveratrol ( AV) can promote the proliferation and colony - form-ing of periodontal ligament stem cells (PDLSCs) derived from aged donors. METHODS: The PDLSCs were acquired from the periodontal ligament tissues of middle - aged and elderly subjects by enzymolysis and cultured in vitro, the PDLSCs were not pretreated(control group) or pretreated by AV (AV group) or nicotinamide(NT group). Cell prolif-eration was determined by MTT assay and colony formation was detected by crystal violet staining. PCR and Western blotting were performed to determine the relative expressions of SIRT1 and HIFl-a. RESULTS : AV pretreatment en-hanced the capacities of proliferation and colony formation of PDLSCs derived from aged donors (P 〈0. 05) , while NT impaired the proliferation and colony formation of the PDLSCs (P 〈 0. 05 ) . The expression of SIRT1 was promoted and the expression of P53 was down - regulated by AV pretreatment (P 〈 0. 05 ) . CONCLUSION : Resveratrol can reverse the proliferation and colony formation of PDLSCs derived from aged donors via the activation of SIRT1.
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