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作 者:薛晶[1] 俞艳[1,2] 王利娟[3] 于金华[1,2] 张光东[1,2]
机构地区:[1]南京医科大学口腔疾病研究江苏省重点实验室,江苏南京210029 [2]南京医科大学附属口腔医院牙体牙髓病科,江苏南京210029 [3]常州市口腔医院牙体牙髓病科,江苏常州213003
出 处:《口腔生物医学》2015年第1期11-14,共4页Oral Biomedicine
基 金:江苏高校优势学科建设工程资助项目(2014-37)
摘 要:目的:探讨中药黄芩苷对牙髓干细胞的增殖、成牙/成骨分化能力的影响。方法:酶消化法原代培养人牙髓干细胞,采用甲基噻唑基四唑(MTT)比色法检测黄芩苷对人牙髓干细胞增殖的影响,碱性磷酸酶活性检测及Western blot等方法检测黄芩苷作用于人牙髓干细胞后,其成牙/成骨分化指标,包括核心结合因子(runt-related transcription factor 2,RUNX2)、牙本质涎蛋白(dentin sialoprotein,DSP)、Osterix(OSX)、骨桥蛋白(osteopontin,OPN)、骨钙素(osteocalcin,OCN)的变化。结果:MTT检测结果显示,0~20μmol/L黄芩苷作用于牙髓干细胞后其增殖能力与对照组相比无明显差异(P〉0.05);而碱性磷酸酶活性检测显示:0~20μmol/L黄芩苷各浓度组细胞ALP活性比对照组明显增加(P〈0.01);Western blot结果表明:与对照组相比,20μmol/L黄芩苷可增强牙髓干细胞RUNX2、DSP、OSX、OPN、OCN等成牙/成骨相关蛋白的表达。结论:黄芩苷对牙髓干细胞的增殖无明显影响,但可促进其成牙/成骨分化能力。Objective: To investigate the effect of baicalin on the proliferation and odento/osteogenic differentiation of huaman dental pulp stem cells( h DPSCs) in vitro. Methods: h DPSCs were isolated from dental pulp and then were cultured in alpha minimun essential medium( α-MEM) supplimented with or without baicalin. MTT colorimetric method was used to examine the proliferation ability of h DPSCs. The effect of baicalin on the odento / osteogenic differentiation was observed by alkaline phosphotase( ALP) activity and Western blot. Results: MTT assay showed that there was no significant difference between baicalin-treated and untreated control cells( P 〉0. 05),and ALP activity assay demonstrated that 0 ~ 20 μmol / L baicalin enhanced the ALP activity of DPSCs( P 〈0. 01),and Western blot revealed that the odento / osteogenic marker( RUNX2,DSP,OSX,OPN,OCN) was significantly upregulated in baicalin-treated cells compared with the untreated cells. Conclusions: Baicalin has no effect on the proliferation of DPSCs,but enhances the capacity of odento / osteogenic differentiation.
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