Feng Li, Li Yehong, Zeng Wenchao, Xia Bo, Zhou Dongsheng, Zhou Jing
Department of Orthopedics, Jining No. 1 People's Hospital, Jining, Shandong 272011, P.R. China.
Department of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250014, P.R. China.
Exp Ther Med. 2017 Dec;14(6):6087-6092. doi: 10.3892/etm.2017.5320. Epub 2017 Oct 17.
The present study aimed to investigate the effects of basic fibroblast growth factor (bFGF) and fibronectin (FN) on adhesion of osteoblasts seeded into bio-derived bone scaffolds. Rat calvarial osteoblasts were separated and their osteogenic phenotypes were determined by staining for alkaline phosphatase as well as alizarin red staining. The bio-derived bone scaffolds were prepared from the metaphysis of porcine femur and their physicochemical properties were assessed by scanning electron microscopy (SEM) and X-ray diffraction analysis. An MTT assay was used to detect the effects of bFGF and FN on osteoblast adhesion or proliferation on cell/scaffold constructs through blocking the extracellular matrix FN-integrin pathway by the Gly-Arg-Gly-Asp-Ser (GRGDS) peptide. Western blot analysis was used to measure the β1 integrin levels. Based on the adhesion of osteoblasts stimulated by various concentrations of bFGF (0.1, 1, 10 and 100 ng/ml) on bio-derived bone scaffolds modified by various concentrations of FN (0.1, 1, 10 and 100 µg/ml), the cell/scaffold constructs were divided into four groups: i) Control, non-stimulated and non-modified group; ii) 10 µg/ml FN-modified group; iii) 100 ng/ml bFGF-stimulated group; iv) 10 µg/ml FN + 100 ng/ml bFGF group. Cell proliferation curves acquired by MTT assay and micrographs obtained by SEM showed that the combination of bFGF and FN significantly improved cell adhesion, particularly in the 10 µg/ml FN + 100 ng/ml bFGF group vs. the other groups, and the effect on cell adhesion was inhibited by 1 mmol/l GRGDS peptide through the FN-integrin pathway. Western blot results showed that the combination of bFGF and FN significantly enhanced β1 integrin expression levels. These results suggested that osteoblasts stimulated by 100 ng/ml bFGF and bio-derived bone materials modified by 10 µg/ml FN should be combined to be applied in the bone tissue engineering.
本研究旨在探讨碱性成纤维细胞生长因子(bFGF)和纤连蛋白(FN)对接种于生物衍生骨支架的成骨细胞黏附的影响。分离大鼠颅骨成骨细胞,并通过碱性磷酸酶染色以及茜素红染色来确定其成骨表型。生物衍生骨支架由猪股骨的干骺端制备而成,其物理化学性质通过扫描电子显微镜(SEM)和X射线衍射分析进行评估。采用MTT法,通过甘氨酸-精氨酸-甘氨酸-天冬氨酸-丝氨酸(GRGDS)肽阻断细胞外基质FN-整合素途径,检测bFGF和FN对细胞/支架构建物上成骨细胞黏附或增殖的影响。采用蛋白质免疫印迹分析来测定β1整合素水平。基于不同浓度的bFGF(0.1、1、10和100 ng/ml)刺激的成骨细胞在不同浓度的FN(0.1、1、10和100 μg/ml)修饰的生物衍生骨支架上的黏附情况,将细胞/支架构建物分为四组:i)对照组,未刺激且未修饰组;ii)10 μg/ml FN修饰组;iii)100 ng/ml bFGF刺激组;iv)10 μg/ml FN + 100 ng/ml bFGF组。通过MTT法获得的细胞增殖曲线以及通过SEM获得的显微照片显示,bFGF和FN的组合显著改善了细胞黏附,特别是在10 μg/ml FN + 100 ng/ml bFGF组与其他组相比时,并且1 mmol/l GRGDS肽通过FN-整合素途径抑制了对细胞黏附的影响。蛋白质免疫印迹结果显示,bFGF和FN的组合显著增强了β1整合素表达水平。这些结果表明,100 ng/ml bFGF刺激的成骨细胞与10 μg/ml FN修饰的生物衍生骨材料应联合应用于骨组织工程。