期刊文献+

富血小板纤维蛋白凝胶析出液对人牙髓细胞体外矿化的影响

The effect of platelet-rich fibrin gel precipitate liquid on mineralization of human dental pulp cells in vitro
下载PDF
导出
摘要 目的探索富血小板纤维蛋白(platelet-rich fibrin,PRF)凝胶析出液对人牙髓细胞(human dental pulp cells,hDPCs)体外矿化的影响。方法组织块法培养hDPCs。采用Choukroun一步离心法制备PRF凝胶。将新鲜制备的PRF凝胶浸泡于DMEM培养基中,于第7d取析出液。用PRF凝胶析出液孵育hDPCs 3d后更换矿化诱导液。采用茜素红染色和RT-PCR检测人牙髓细胞矿化的潜能。结果矿化诱导21d后,茜素红染色观察到实验组有少量钙结节生成,而对照组无钙结节生成;RT-PCR结果显示,实验组hDPCs碱性磷酸酶(ALP)的表达为对照组的1.5倍,差异具有统计学意义(P<0.05)。结论 PRF凝胶析出液可促进人牙髓细胞矿化。 Objective This study was designed to investigate the effect of platelet-rich fibrin gel (PRF gel)precipitate liquid on the mineralization of human dental pulp cells (hDPCs)in vitro. Methods The hD-PCs were separated and cultured by using tissue block culture method.PRF gel was prepared by Choukroun&#39;s protocols.The newly prepared PRF gel was dipped in DMEM culture media,the precipitate liquid of PRF gel was collected on day 7.hDPCs were treated with mineralization induction solution 3 days after being incubated with the precipitate liquid of PRF gel.The capacity of mineralization was measured by using alizarin red stai-ning and RT-PCR. Results Twenty-one days after mineralization induction,a small amount of mineral-ized nodules on alizarin red staining were observed in experimental group while no mineralized nodule was ob-served in control group;RT-PCR revealed that the expression of alkaline phosphatase (ALP)in experimental group was 1.5 times higher than that in control group,comparison yielded statistical difference (P 〈0.05). Conclusion The precipitate liquid of PRF gel can accelerate the mineralization of hDPCs.
出处 《右江民族医学院学报》 2015年第3期349-351,共3页 Journal of Youjiang Medical University for Nationalities
基金 国家自然科学基金资助项目(81160133)
关键词 富血小板纤维蛋白凝胶 析出液 人牙髓细胞 矿化 platelet-rich fibrin gel precipitate liquid human dental pulp cells mineralization
  • 相关文献

参考文献1

二级参考文献68

  • 1Belema-Bedada F, Uchida S, Martire A, Kostin S, Braun T. Efficient homing of multipotent adult mesenchymal stem cells depends on FROUNT-mediated clustering of CCR2. CellStem Cell 2008; 2: 566-575. 被引量:1
  • 2Kitaori T, Ito H, Schwarz EM, et al. Stromal cell-derived factor 1/CXCR4 signaling is critical for the recruitment of mesenchymal stem cells to the fracture site during skeletal repair in a mouse model. Arthritis Rheum 2009; 60: 813- 823. 被引量:1
  • 3Goldberg M, Six N, Decup F, et al. Application ofbioactive molecu|es in pulp-capping situations. Adv Dent Res 2001; 15: 91-95. 被引量:1
  • 4Rutherford RB. BMP-7 gene transfer to inflamed ferret dental pulps. Eur J Oral Sci 2001; 109: 422-424. 被引量:1
  • 5White AP, Vaccaro AR, Hall JA, et al. Clinical applications of BMP-7/OP-1 in fractures, nonunions and spinal fusion. Int Orthop 2007; 31: 735-741. 被引量:1
  • 6Nait Lechguer A, Kuchler-Bopp S, Hu B, HaYkel Y, Lesot H Vascularization of engineered teeth. J Dent Res 2008; 87 1138-1143. 被引量:1
  • 7Hahn GV, Cohen RB, Wozney JM, et al. A bone morphogenetic protein subfam@: chromosomal localization of human genes for BMP5, BMP6, and BMP7. Genomics 1992; 14: 759-762. 被引量:1
  • 8ltoh F, Asao H, Sugamura K, et al. Promoting bone morphogenetic protein signaling through negative regulation of inhibitory Smads. EMBOJ2001; 20: 4132-4142. 被引量:1
  • 9Lee CH, Cook JL, Mendelson A, et al. Regeneration of the articular surface of the rabbit synovial joint by cell homing: a proof of concept study. Lancet 2010; 376: 440-448. 被引量:1
  • 10Yelick PC, Vacanti JP. Bioengineered teeth from tooth bud cells. Dent Clin North Am 2006; 50: 191-203. 被引量:1

共引文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部