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机构地区:[1]第四军医大学口腔医学院,陕西西安710032 [2]深圳市宝安区龙华人民医院口腔科,广东深圳518109 [3]国防科学技术大学医院口腔科,湖南长沙410073
出 处:《牙体牙髓牙周病学杂志》2013年第7期450-453,共4页Chinese Journal of Conservative Dentistry
摘 要:目的:研究碱性成纤维细胞生长因子(basic fibroblast growth factor,bFGF)对体外培养的人牙髓细胞(human dental pulp cells,HDPCs)生物学活性的影响。方法:常规组织块培养法获得HDPCs,采用四唑盐比色(MTT)法、ALP活性检测法观察不同浓度bFGF(0.1、1、10、100μg/L)对体外培养的HDPC粘附性、伸展性以及ALP活性的影响。结果:不同浓度bFGF均可提高HDPCs粘附性和伸展性,与对照组相比P<0.05;不同浓度bFGF与HDPCs共同培养一定时间后,均能显著抑制其ALP活性(P<0.05);并且浓度越高,抑制作用出现的时间越早,100μg/L组在培养第1天时与对照组相比P<0.05。结论:0.1~100μg/L范围内不同浓度bFGF均能促进HDPCs的粘附性和伸展性,并可抑制HDPCs的ALP活性。AIM: To investigate the effects of basic fibroblast growth factor (bFGF) on the biologic activity of human dental pulp cells (HDPCs) in vitro. METHODS : HDPCs were obtained from extracted human premolar and cultured in DMEM medium with 10% fetal bovine serum (FBS). The cells were treated by bFGF at 0. 1 μg/L, 1μg/L, 10μg/L and 100 μg/L respectively. Ceil attachment assay and spreading assay were conducted. Alkaline phosphatase (ALP) activity of the ceils was examined by enzyme dynamics method. RESULTS: bFGF at 0. 1 μg/L 1 μg/L, 10 μg/L and 100 μg/L promoted the attachment ability and the spreading rate of HDPCs ( vs control, P 〈 0.05 ), and suppressed ALP activity of the ceils (vs control P 〈 0.05 ) in a dose -and time-dependent manner. CONCLUSION: bFGF can increase the attachment ability and spreading rate , and decrease ALP activity of of HDPCs.
关 键 词:碱性成纤维细胞生长因子 人牙髓细胞 生物学活性
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