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富血小板纤维蛋白进阶版与可注射富血小板纤维蛋白对根尖乳头干细胞增殖、迁移及分化的疗效比较

The efficacy of advanced platelet-rich fibrin plus versus injectable platelet-rich fibrin on the proliferation, migration, and differentiation of stem cells from apical papilla.

作者信息

Le Son Hoang, Nguyen Son Hong

机构信息

Department of Oral Surgery, Faculty of Odonto-Stomatology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Viet Nam.

出版信息

J Dent Sci. 2024 Oct;19(4):2203-2209. doi: 10.1016/j.jds.2024.03.008. Epub 2024 Mar 15.

DOI:10.1016/j.jds.2024.03.008
PMID:39347039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11437258/
Abstract

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).

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

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。

材料与方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/2723a71e7a53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/8089962375f0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/ebca2e01b396/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/2723a71e7a53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/8089962375f0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/ebca2e01b396/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d640/11437258/2723a71e7a53/gr3.jpg

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