Le Son Hoang, Nguyen Son Hong
Department of Oral Surgery, Faculty of Odonto-Stomatology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Viet Nam.
J Dent Sci. 2024 Oct;19(4):2203-2209. doi: 10.1016/j.jds.2024.03.008. Epub 2024 Mar 15.
BACKGROUND/PURPOSE: Platelet-rich fibrin (PRF) is a promising host-derived scaffold for regenerative endodontic treatment. This study investigated the effects of advanced PRF plus (A-PRF+) and injectable PRF (i-PRF) on the proliferation, migration, and differentiation of stem cells from apical papilla (SCAPs).
A-PRF+ and i-PRF were prepared using a DUO Quattro centrifuge following a standard protocol. A-PRF+ and i-PRF extract were diluted in Dulbecco's modified Eagle's medium and Ham's F-12 medium (DMEM/F12) to produce the experimental culture medium. DMEM/F12 and DMEM/F12 supplemented with 10% foetal bovine serum (FBS) were used as the negative control (NC) and positive control (PC) media, respectively. The proliferative ability of SCAPs was assessed using a counting method (haemocytometer). The migration ability was examined using a scratch-wound assay. , , , and expression were measured to determine the differentiation ability.
The proliferation, migration, and differentiation of SCAPs in the A-PRF+ group were similar to those of the PC group. In the i-PRF group, the cell number was significantly (p < 0.01) lower than that of the A-PRF+ group on days 8 and 10; the percentage of the scratched area on days 1 and 2 was significantly higher than in the A-PRF+ group (p < 0.05). The mRNA expression levels of biomarkers in the i-PRF group were similar to those in the A-PRF+ group.
Both A-PRF+ and i-PRF induce SCAPs proliferation, migration, and differentiation. However, A-PRF+ was superior in supporting the proliferation and migration of SCAPs.
背景/目的:富血小板纤维蛋白(PRF)是一种很有前景的用于再生性牙髓治疗的宿主来源支架材料。本研究调查了高级PRF plus(A-PRF+)和可注射PRF(i-PRF)对根尖乳头干细胞(SCAPs)增殖、迁移及分化的影响。
按照标准方案使用DUO Quattro离心机制备A-PRF+和i-PRF。将A-PRF+和i-PRF提取物在杜氏改良 Eagle培养基和哈姆F-12培养基(DMEM/F12)中稀释以制备实验培养基。DMEM/F12和补充有10%胎牛血清(FBS)的DMEM/F12分别用作阴性对照(NC)和阳性对照(PC)培养基。使用计数法(血细胞计数器)评估SCAPs的增殖能力。使用划痕试验检测迁移能力。检测 、 、 和 的表达以确定分化能力。
A-PRF+组中SCAPs的增殖、迁移和分化与PC组相似。在i-PRF组中,第8天和第10天的细胞数量显著低于A-PRF+组(p < 0.01);第1天和第2天划痕区域的百分比显著高于A-PRF+组(p < 0.05)。i-PRF组中生物标志物的mRNA表达水平与A-PRF+组相似。
A-PRF+和i-PRF均可诱导SCAPs增殖、迁移和分化。然而,A-PRF+在支持SCAPs的增殖和迁移方面更具优势。