Healthcare and Energy Materials Laboratory, Faculty of Engineering, National University of Singapore, Singapore.
J Biomater Sci Polym Ed. 2013;24(2):170-84. doi: 10.1163/156856212X629845. Epub 2012 May 11.
Electrospraying of hydroxyapatite (HA) nanoparticles onto the surface of polymer nanofibers provides a potentially novel substrate for the adhesion, proliferation and differentiation of mesenchymal stem cells (MSCs) into bone tissue regeneration. HA nanoparticles (4%) were electrosprayed on the surface of electrospun polycaprolactone (PCL) nanofibers (420 ± 15 nm) for bone tissue engineering. PCL/HA nanofibers were comparatively characterized with PCL/Collagen (275 ± 56 nm) nanofibers by FT-IR analysis to confirm the presence of HA. Fabricated PCL/HA and PCL/Collagen nanofibers and TCP (control) were used for the differentiation of equine MSC into osteogenic lineages in the presence of DMEM/F12 medium supplemented with β-glycerophosphate, ascorbic acid and dexamethasone. Cell proliferation and differentiation into an osteogenic lineage was evaluated by MTS assay, SEM observation, ALP activity, ARS staining, quantification of mineral deposition and expression of osteocalcin. Proliferation of MSCs increased significantly (P ⩽ 0.05) up to 12% in PCL/Collagen (day 15) compared to PCL/HA nanofibrous substrate. ALP activity was increased 20% in PCL/HA by day 10 confirming the direction of osteogenic lineage from MSCs differentiation. PCL/HA stimulated an increased mineral secretion up to 26% by day 15 on ARS staining compared to PCL/Collagen nanofibers and showing cuboidal morphology by expressing osteocalcin. These results confirmed that the specifically fabricated PCL/HA composite nanofibrous substrate enhanced the differentiation of MSCs into osteogenesis.
将羟基磷灰石 (HA) 纳米粒子电喷到聚合物纳米纤维的表面上,为间充质干细胞 (MSCs) 向骨组织再生中的黏附、增殖和分化提供了一种潜在的新型基质。将 HA 纳米粒子 (4%) 电喷到静电纺丝的聚己内酯 (PCL) 纳米纤维 (420 ± 15nm) 的表面上,用于骨组织工程。通过傅里叶变换红外分析 (FT-IR) 对 PCL/HA 纳米纤维进行比较表征,以确认 HA 的存在。用 FT-IR 分析对制备的 PCL/HA 和 PCL/Collagen (275 ± 56nm) 纳米纤维进行比较,以确认 HA 的存在。用 DMEM/F12 培养基补充 β-甘油磷酸、抗坏血酸和地塞米松,将马 MSC 分化为成骨谱系,评估细胞增殖和成骨谱系分化。通过 MTS 测定、SEM 观察、碱性磷酸酶 (ALP) 活性、ARS 染色、矿物质沉积定量和骨钙蛋白表达评估 MSC 增殖和成骨谱系分化。与 PCL/HA 纳米纤维基质相比,PCL/Collagen 纳米纤维上 MSC 的增殖在第 15 天显著增加 (P ⩽ 0.05),达到 12%。ALP 活性在第 10 天增加了 20%,证实了 MSC 分化为成骨谱系的方向。与 PCL/Collagen 纳米纤维相比,PCL/HA 在第 15 天的 ARS 染色上刺激了高达 26%的矿物质分泌,并通过表达骨钙蛋白呈现出立方体形。这些结果证实,特定制备的 PCL/HA 复合纳米纤维基质增强了 MSC 向成骨分化的分化。