摘要
目的:探讨肿瘤坏死因子-α(TNF-α)对根尖乳头干细胞(SCAP)外增殖及成牙成骨向分化能力的影响。方法:采用酶消化法结合组织块法获得根尖乳头干细胞,免疫荧光免疫组化法鉴定细胞来源,通过不同浓度的TNF-α进行干预后检测对SCAP增殖,矿化成牙成骨能力的影响。结果:MTT检测显示各浓度组TNF-α均能刺激SCAP的体外增殖,10、50mg/L的TNF-α实验组可明显促进SCAP增殖(P<0.05),差异具有统计学意义;茜素红染色显示与对照组(0mg/L TNF-α)相比,实验组(5、10、50mg/L TNF-α)染色明显变浅,矿化结节形成的较小,对照组形成红色结节范围大且呈深橘色;免疫组化染色显示SCAP胞浆中DSP、BSP均有表达,实验组部分细胞胞浆染色且染色较浅,呈褐色为阳性表达,对照组(0 mg/L TNF-α)细胞胞浆完全着色呈深褐色,为强阳性表达。结论:不同浓度TNF-α对SCAP的生长增殖均有促进作用,TNF-α在不同程度上对SCAP矿化及成牙成骨向分化有抑制作用。
Objective:To investigate the effects of TNF-αon the proliferation and odontoblastic and osteogenic differentiation of stem cells from the apical papilla(SCAP)in vitro.Methods:Stem cells were isolated from the apical papillary by combining enzyme digestion with tissue block method,and identified by immunofluorescence and immunocytochemical method.After treated by TNF-α,the effect on the proliferation and mineralized tooth's ontogenesis ability were detected in SCAP.Results:TNF-αin each density group can stimulate the proliferation of SCAP in vitro,particularly in 10mg/L and 50mg/L(P〈0.05).Additionally,in the experimental group,the Alizarin red staining was obvious weaker with smaller mineral node,and the expression of DSP and BSP were downregulated compared to the control group.Conclusion:TNF-αcould promote the proliferation and inhibit the mineralization of SCAP.
出处
《口腔医学研究》
CAS
CSCD
北大核心
2016年第4期343-346,共4页
Journal of Oral Science Research
基金
新疆维吾尔自治区自然科学基金(编号:2015211C107)