碱性成纤维细胞生长因子以治疗依赖的方式影响牙髓干细胞的成骨分化。
Basic fibroblastic growth factor affects the osteogenic differentiation of dental pulp stem cells in a treatment-dependent manner.
机构信息
State Key Laboratory of Military Stomatology, Department of Operative Dentistry & Endodontics, School of Stomatology, Fourth Military Medical University, Xi'an, Shaanxi, China.
Hospital of Stomatology, The Zunyi Medical University, Zunyi, Guizhou, China.
出版信息
Int Endod J. 2015 Jul;48(7):690-700. doi: 10.1111/iej.12368. Epub 2014 Sep 11.
AIM
To determine how basic fibroblastic growth factor (bFGF) affected the osteogenic differentiation of human dental pulp stem cells (DPSCs) in vitro and in vivo.
METHODOLOGY
Basic fibroblastic growth factor stimulation of DPSCs was divided into a pre-treatment period and an osteogenic differentiation period. Alizarin red quantification experiments and alkaline phosphatase activity quantification assay were performed to examine the osteogenic differentiation of DPSCs after different bFGF stimulation. Quantification reverse transcription polymerase chain reaction was used to analyze the osteogenic gene expression of DPSCs after different bFGF stimulation. In addition, DPSCs that received the 1 and 2 weeks bFGF pre-treatments as in the in vitro experiments were mineralized for 1 week and seeded into hydroxyapatite/tricalcium phosphate (HA/TCP) pills and subcutaneously transplanted into naked mice for 2 or 3 months. The transplants were removed, sliced and stained using Modified Ponceau Trichrome Stain to observe the formation of mineralized tissue.
RESULTS
Basic fibroblastic growth factor stimulation in the osteogenic differentiation period decreased the in vitro osteogenic differentiation ability of DPSCs. One week pre-treatment with bFGF increased the in vitro osteogenic differentiation ability of DPSCs, whereas 2 weeks pre-treatment with bFGF decreased the in vitro osteogenic differentiation ability of DPSCs. The pre-treatment period was vital for the osteogenic differentiation of DPSCs in vitro. The in vivo results were similar to the in vitro results.
CONCLUSIONS
Basic fibroblastic growth factor affected the osteogenic differentiation of DPSCs in a treatment-dependent manner both in vitro and in vivo.
目的
探讨碱性成纤维细胞生长因子(bFGF)对人牙髓干细胞(DPSCs)体外和体内成骨分化的影响。
方法
将碱性成纤维细胞生长因子刺激 DPSCs 分为预处理期和成骨分化期。茜素红定量实验和碱性磷酸酶活性定量检测用于检测不同 bFGF 刺激后 DPSCs 的成骨分化。采用定量逆转录聚合酶链反应分析不同 bFGF 刺激后 DPSCs 的成骨基因表达。此外,将接受 1 周和 2 周 bFGF 预处理的 DPSCs 进行矿化培养 1 周,然后接种到羟基磷灰石/磷酸三钙(HA/TCP)丸剂中,皮下移植到裸鼠体内 2 或 3 个月。取出移植体,切片,用改良品红三苯甲烷染色观察矿化组织的形成。
结果
成骨分化期碱性成纤维细胞生长因子刺激降低了 DPSCs 的体外成骨分化能力。bFGF 预处理 1 周增加了 DPSCs 的体外成骨分化能力,而 bFGF 预处理 2 周降低了 DPSCs 的体外成骨分化能力。预处理期对 DPSCs 的体外成骨分化至关重要。体内结果与体外结果相似。
结论
碱性成纤维细胞生长因子以依赖于处理的方式影响 DPSCs 的体外和体内成骨分化。