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富血小板纤维蛋白和低强度激光介导的根尖乳头干细胞的成骨潜能

Osteogenic potential of apical papilla stem cells mediated by platelet-rich fibrin and low-level laser.

作者信息

Ramírez David Gutiérrez, Inostroza Carolina, Rouabhia Mahmoud, Rodriguez Camilo Alfonso, Gómez Lina Andrea, Losada Mónica, Muñoz Ana Luisa

机构信息

Buccal Innovation Research Group, Faculty of Dentistry, Universidad Antonio Nariño, Popayán, Colombia.

Facultad de Odontología, Universidad de los Andes, Santiago, Chile.

出版信息

Odontology. 2024 Apr;112(2):399-407. doi: 10.1007/s10266-023-00851-8. Epub 2023 Oct 24.

Abstract

To evaluate the osteogenic potential of platelet-rich fibrin (PRF) and low-level laser therapy (LLLT) on human stem cells from the apical papilla (SCAP) we isolated, characterized, and then cultured in an osteogenic medium cells with PRF and/or LLLT (660 nm, 6 J/m2-irradiation). Osteogenic differentiation was assessed by bone nodule formation and expression of bone morphogenetic proteins (BMP-2 and BMP-4), whereas the molecular mechanisms were achieved by qRT-PCR and RNA-seq analysis. Statistical analysis was performed by ANOVA and Tukey's post hoc tests (p < 0.05* and p < 0.01**). Although PRF and LLLT increased bone nodule formation after 7 days and peaked at 21 days, the combination of PRF + LLLT led to the uppermost nodule formation. This was supported by increased levels of BMP-2 and -4 osteogenic proteins (p < 0.005). Furthermore, the PRF + LLLT relative expression of specific genes involved in osteogenesis, such as osteocalcin, was 2.4- (p = 0.03) and 28.3- (p = 0.001) fold higher compared to the PRF and LLLT groups, and osteopontin was 22.9- and 1.23-fold higher, respectively (p < 0.05), after 7 days of interaction. The transcriptomic profile revealed that the combination of PRF + LLLT induces MSX1, TGFB1, and SMAD1 expression, after 21 days of osteogenic differentiation conditions exposition. More studies are required to understand the complete cellular and molecular mechanisms of PRF plus LLLT on stem cells. Overall, we demonstrated for the first time that the combination of PRF and LLLT would be an excellent therapeutic tool that can be employed for dental, oral, and craniofacial repair and other tissue engineering applications.

摘要

为了评估富血小板纤维蛋白(PRF)和低强度激光疗法(LLLT)对人根尖乳头干细胞(SCAP)的成骨潜力,我们对分离出的细胞进行了鉴定,然后将其置于成骨培养基中,分别用PRF和/或LLLT(660nm,6J/m²照射)进行培养。通过骨结节形成和骨形态发生蛋白(BMP - 2和BMP - 4)的表达来评估成骨分化,而分子机制则通过qRT - PCR和RNA测序分析来实现。采用方差分析和Tukey事后检验进行统计分析(p < 0.05和p < 0.01*)。虽然PRF和LLLT在7天后增加了骨结节形成,并在21天达到峰值,但PRF + LLLT组合导致了最高的结节形成。这得到了BMP - 2和 - 4成骨蛋白水平升高的支持(p < 0.005)。此外,在相互作用7天后,与PRF组和LLLT组相比,PRF + LLLT组中参与成骨的特定基因(如骨钙素)的相对表达分别高2.4倍(p = 0.03)和28.3倍(p = 0.001),骨桥蛋白分别高22.9倍和1.23倍(p < 0.05)。转录组分析表明,在成骨分化条件暴露21天后,PRF + LLLT组合诱导了MSX1、TGFB1和SMAD1的表达。需要更多的研究来了解PRF加LLLT对干细胞的完整细胞和分子机制。总体而言,我们首次证明PRF和LLLT的组合将是一种出色的治疗工具,可用于牙科、口腔和颅面修复以及其他组织工程应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3240/10925562/0e92f8670fbc/10266_2023_851_Fig1_HTML.jpg

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