Clinic for Oral and Maxillofacial Surgery, University of Marburg, Marburg, Germany.
Clin Oral Implants Res. 2013 Jul;24(7):750-7. doi: 10.1111/j.1600-0501.2012.02481.x. Epub 2012 Apr 24.
Combination of scaffolds and growth factors is a promising option for several clinical problems in bone biomaterials. Simplified growth factor loading by adsorption from aqueous solution is one important option for this technology. We evaluated the adsorption followed by PBS rinsing, release and biological effect of transient loading with basic fibroblast growth factor (bFGF) and bone morphogenic protein 2 (BMP-2) on fresh frozen bone, processed bone matrix, collagen, and a ceramic material with immunofluorescence, enzyme-linked immunosorbent assay (ELISA), and qRT-PCR.
The study consisted of three in vitro experiments (immunofluorescence, ELISA, and qRT-PCR) in human osteoblasts (HOB). The first evaluated the adsorption of the growth factors bFGF and BMP-2 to the biomaterials, analyzed by immunofluorescence assays. The second experiment used ELISA to analyze the release of the growth factors from the matrix. The biological effect of the growth factors on HOB was then studied with qRT-PCR experiments as the third step.
Strongest sustained release peaks in ELISA were observed in bFGF loading on processed bone matrix (steam-resistant mineralized bone matrix, SMBM) with up to 553 pg/ml medium. BMP-2 loading was less effective in ELISA peak release experiments with up to 257 pg/ml medium in processed bone matrix (SMBM). bFGF showed also higher release peaks in collagen material (192 pg/ml) compared with BMP-2 (101 pg/ml). Cumulative release values 0-72 h were estimated. The expression of runX2, osteocalcin, and alkaline phosphatase as markers for osteoblast activity was correlating.
The results showed sustained release of BMP-2 and bFGF after transient loading on bone biomaterials with a stronger effect in biological scaffolds. This is interesting for therapeutic growth factor loading as well as insights in natural growth factor matrix deposition during bone healing.
支架与生长因子的结合是骨生物材料中几个临床问题的有前途的选择。通过从水溶液中吸附来简化生长因子的加载是该技术的重要选择之一。我们通过免疫荧光、酶联免疫吸附测定(ELISA)和 qRT-PCR 评估了碱性成纤维细胞生长因子(bFGF)和骨形态发生蛋白 2(BMP-2)在新鲜冷冻骨、加工骨基质、胶原和陶瓷材料上的瞬态负载吸附、PBS 冲洗、释放和生物学效应。
该研究由三个体外实验(免疫荧光、ELISA 和 qRT-PCR)组成,在人成骨细胞(HOB)中进行。第一项实验评估了生长因子 bFGF 和 BMP-2 对生物材料的吸附,通过免疫荧光分析进行分析。第二项实验使用 ELISA 分析生长因子从基质中的释放。然后,通过 qRT-PCR 实验研究生长因子对 HOB 的生物学效应,作为第三步。
在 ELISA 中观察到 bFGF 在加工骨基质(蒸汽抗性矿化骨基质,SMBM)上的最强持续释放峰,达到 553 pg/ml 培养基。BMP-2 在加工骨基质(SMBM)中的负载效果较差,在 ELISA 峰值释放实验中达到 257 pg/ml 培养基。bFGF 在胶原材料中的释放峰值也高于 BMP-2(192 pg/ml)。0-72 小时的累积释放值被估计。RunX2、骨钙素和碱性磷酸酶作为成骨细胞活性标志物的表达呈正相关。
结果表明,BMP-2 和 bFGF 在骨生物材料上的短暂负载后具有持续释放,在生物支架中具有更强的效果。这对于治疗性生长因子负载以及在骨愈合过程中天然生长因子基质沉积的见解都很有趣。