《Journal of Oral and Maxillofacial Surgery》 ›› 2014, Vol. 24 ›› Issue (2): 102-. doi: 10.3969/j.issn.1005-4979.2014.02.004

• Basic Scientific Study • Previous Articles     Next Articles

Effects of Choukroun′s Platelet-Rich Fibrin on the Osteogenic
Differentiation of Dog Dental Pulp Cells in vitro

YU Jia, HAO Yong-ming, LU Jia-yu, ZHAO Wei, CAO Chun-hua, ZOU De-rong   

  1. Department of Stomatology, Sixth People's Hospital, Shanghai
    Jiaotong University, Shanghai 200233, China
  • Online:2014-04-28 Published:2014-06-27

富血小板纤维蛋白对牙髓细胞增殖与分化的影响

于佳,   郝永明,   陆家瑜,   赵伟,   曹春花,   邹德荣   

  1. 上海交通大学附属第六人民医院口腔科,上海   200233
  • 通讯作者: 邹德荣,教授. E-mail:derongzou@gtmail.com
  • 作者简介:于佳(1987—),女,山东人,硕士研究生. E-mail: jojygirl@hotmail.com
  • 基金资助:

    上海市基础研究项目(12ZR1447200);上海市科委基础研究重点项目(12JC1407300);上海市卫生局青年研究项目(20134Y192)

Abstract: Objective: To evaluate the effects of choukroun's PRF (platelet-rich fibrin) on proliferation and differentiation of dental pulp cells in vitro and making a pre-feasibility assess hunting for the optimum scaffold. Methods: Pulp tissues of deciduous and permanent molars were harvested from 3-month and 16-month old beagle dogs respectively. Dental pulp cells were isolated and cloned. Jugular vein blood were collected from beagle dogs and centrifugation at 3 000 r/min for 10 minutes to obtain PRF. The experiments were divided into four groups: control group (ordinary medium without PRF),  test group A ( ordinary medium with PRF), test group B (osteoinduction medium without PRF), test group C(added PRF in osteoinduction medium ). Cell counts and cytotoxicity tests, semi-quantitative alkaline phosphatase and real time PCR, were performed and assayed at days 1, 4, 7 and 11 of culture. The determination of calcium nodules OD value was in day 21. Results: PRF is a fibrin matrix structure and showed absence of toxic effect on two types of cells. PRF increased a significant proliferation in all cell types. Furthermore, PRF increased a strong differentiation of dental pulp cells including calcium nodules, ALP semi-quantitative(P<0.05) and osteogenesis related genes(P<0.05). Dental pulp cells of exfoliated deciduous teeth showed more obvious than the permanent dental pulp cells.    Conclusion: This in vitro study suggests that PRF scaffolds may be used as a specific regulator of hard-tissue engineering.

Key words: platelet-rich fibrin(PRF), beagle dog, dental pulp cells , cell proliferation and differentiation, tissue engineering

摘要: 目的:评估牙髓细胞在富血小板纤维蛋白(platelet-rich fibrin, PRF)存在下的体外增殖及成骨分化的能力,为PRF作为支架材料、牙髓细胞作为种子细胞构建组织工程骨,进行前期研究。方法:3月龄比格犬拔除乳磨牙获得乳牙牙髓细胞;恒牙牙髓细胞从16月龄成年比格犬磨牙获得。静脉取血离心10 min获得PRF。实验分4组:对照组(普通培养基不加入PRF);实验组A(普通培养基加入PRF);实验组B(成骨诱导培养基不加入PRF);实验组C(成骨诱导培养基加入PRF)。分别于1、4、7和11d测定细胞数量、MTT值、半定量碱性磷酸酶值、成骨相关基因Q?鄄PCR值,并于21d测定钙结节吸光度值。结果:PRF是一种可以促进牙髓细胞增殖的,无毒性作用的纤维网状支架结构;细胞水平上PRF促进了两种细胞的成骨分化:钙结节以及碱性磷酸酶半定量数值都明显上调(P<0.05);基因水平上,4个时间点成骨相关基因的表达量都显著增加(P<0.05),且乳牙牙髓细胞的表现均优于恒牙牙髓细胞。结论:可使用PRF和牙髓细胞复合构建组织工程骨。

关键词: 富血小板纤维蛋白;  , 比格犬;  , 牙髓细胞;  , 增殖和成骨分化;  , 组织工程

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