Choukroun's platelet-rich fibrin (PRF) stimulates in vitro proliferation and differentiation of human oral bone mesenchymal stem cell in a dose-dependent way

被引:185
作者
Ehrenfest, David M. Dohan [1 ,2 ]
Doglioli, Pierre [3 ]
de Peppo, Giuseppe M. [1 ]
Del Corso, Marco [2 ]
Charrier, Jean-Baptiste [2 ,4 ]
机构
[1] Gothenburg Univ, Dept Biomat, Inst Clin Sci, Sahlgrenska Acad, S-41390 Gothenburg, Sweden
[2] LoB5 Fdn Res, Paris, France
[3] Jules Ferry Inst, Cell Culture Lab, Cannes, France
[4] Univ Paris Sud, Dept ENT Head & Neck Surg, Bicetre Hosp, AP HP, F-94275 Le Kremlin Bicetre, France
关键词
Coculture; Growth factors; Leukocyte; Platelet concentrate; Mesenchymal stem cell; Platelet-rich fibrin (PRF); Platelet-rich plasma (PRP); TISSUE-ENGINEERED BONE; SIMULTANEOUS IMPLANT PLACEMENT; MARROW STROMAL CELLS; GROWTH-FACTORS; DISTRACTION OSTEOGENESIS; GRAFTING MATERIAL; INJECTABLE BONE; PLASMA PRP; REGENERATION; OSTEOBLASTS;
D O I
10.1016/j.archoralbio.2010.01.004
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Choukroun's platelet-rich fibrin (PRF) is an autologous leukocyte- and platelet-rich fibrin biomaterial. The purpose of this study was to analyse the in vitro effects of PRF on human bone mesenchymal stem cells (BMSC), harvested in the oral cavity after preimplant endosteal stimulation. Materials and methods: BMSCs from primary cultures were cultivated with or without a PRF membrane originating from the same donor as for the cells, in proliferation or osteoblastic differentiation conditions. After 7 days, the PRF membranes were removed. A series of cultures were performed using 2 PRF membranes, in order to measure the dose-dependent effect. Cell counts, cytotoxicity tests, alkaline phosphatase (ALP) activity quantification, Von Kossa staining and mineralisation nodules counts were performed at 3, 7, 14,21 and 28 days. A last independent series was carried on up to 14 days, for a morphological scanning electron microscope (SEM) observation. Results: PRF generated a significant stimulation of the BMSc proliferation and differentiation throughout the experimental period. This effect was dose-dependent during the first weeks in normal conditions, and during the whole experimentation in differentiation conditions. The cultures without PRF in differentiation conditions did not rise above the degree of differentiation of the cultures in normal conditions with 1 or 2 PRF up to the 14th and 28th day, respectively. The SEM culture analysis at day 14 allowed to show the mineralisation nodules which were more numerous and more structured in the groups with PRF compared to the control groups. Discussion and conclusions: This double contradictory proliferation/differentiation resultmaybe due to the numerous components of PRF, particularly the presence of leukocytes: any culture with PRF is in fact a coculture with leukocytes. It could be the source of differential geographic regulation processes within the culture. The combination of oral BMSC and PRF might offer many potential clinical and biotechnological applications, and deserves new studies. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 194
页数:10
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