The role of fibroblast growth factor-2 in modulating the differentiation of periodontal ligament and alveolar bone-derived stem cells

IF 2.2 4区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Benjamin Sexton , Yuanyuan Han , Renan Dal-Fabbro , Jinping Xu , Darnell Kaigler , Marco C. Bottino
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Abstract

Objective

This study examined how range concentrations of Fibroblast Growth Factor-2 (FGF-2) influence the differentiation and activity of human-derived periodontal ligament (hPDLSCs) and alveolar bone-derived stem cells (haBMSCs).

Design

hPDLSCs and haBMSCs were cultured with varying concentrations of FGF-2 (0, 1, 2.5, 5, 10, 20 ng/mL) and monitored for osteogenic differentiation through alkaline phosphatase (ALP) activity and quantification of gene expression (qRT-PCR) for osteogenesis markers. Additionally, alizarin red staining and a hydroxyproline colorimetric assay evaluated and quantified osteogenic matrix mineralization and collagen deposition. Statistical analyses were performed using one-way ANOVA or two-way ANOVA for multiple comparisons between groups.

Results

At low FGF-2 concentrations, hPDLSCs differentiated toward an osteogenic lineage, whereas higher concentrations of FGF-2 inhibited osteogenesis and promoted fibroblastic differentiation. The effect of FGF-2 at the lowest concentration tested (1 ng/mL) led to significantly higher ALP activity than osteogenically induced positive controls at early time points and equivalent RUNX2 expression at early and later time points. FGF-2 supplementation of haBMSC cultures was sufficient, at all concentrations, to increase ALP activity at an earlier time point. Mineralization of haBMSC cultures increased significantly within 5–20 ng/mL FGF-2 concentrations under basal growth media conditions (α-minimal essential medium supplemented with 15 % fetal bovine serum and 1 % penicillin/streptomycin).

Conclusions

FGF-2 has a dual capacity in promoting osteogenic and fibroblastic differentiation within hPDLSCs contingent upon the dosage and timing of administration, alongside supporting osteogenic differentiation in haBMSCs. These findings underscore the need for precision growth factors dosing when considering the design of biomaterials for periodontal regeneration.

成纤维细胞生长因子-2 在调节牙周韧带和牙槽骨来源干细胞分化中的作用
本研究探讨了成纤维细胞生长因子-2(FGF-2)的浓度范围如何影响人源性牙周韧带干细胞(hPDLSCs)和牙槽骨源性干细胞(haBMSCs)的分化和活性。用不同浓度的FGF-2(0、1、2.5、5、10、20纳克/毫升)培养DesignhPDLSCs和haBMSCs,并通过碱性磷酸酶(ALP)活性和成骨标记基因表达定量(qRT-PCR)监测其成骨分化。此外,茜素红染色和羟脯氨酸比色法评估并量化了成骨基质矿化和胶原沉积。结果低浓度的FGF-2能使hPDLSCs向成骨系分化,而高浓度的FGF-2则抑制成骨,促进成纤维细胞分化。在测试的最低浓度(1 毫微克/毫升)下,FGF-2 的作用导致早期时间点的 ALP 活性明显高于成骨诱导阳性对照,早期和后期时间点的 RUNX2 表达相当。在所有浓度下,对 haBMSC 培养物补充 FGF-2 都足以在较早的时间点提高 ALP 活性。结论FGF-2具有促进hPDLSCs成骨和成纤维分化的双重能力,这取决于给药的剂量和时间,同时也支持haBMSCs的成骨分化。这些发现突出表明,在考虑设计牙周再生生物材料时,需要精确的生长因子剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of oral biology
Archives of oral biology 医学-牙科与口腔外科
CiteScore
5.10
自引率
3.30%
发文量
177
审稿时长
26 days
期刊介绍: Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including: Cell and molecular biology Molecular genetics Immunology Pathogenesis Cellular microbiology Embryology Syndromology Forensic dentistry
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