In vitro osteogenic induction of bone marrow mesenchymal stem cells with a decellularized matrix derived from human adipose stem cells and in vivo implantation for bone regeneration

去细胞化 间充质干细胞 干细胞 细胞生物学 脂肪组织 干细胞移植修复关节软骨 体外 体内 骨髓 再生(生物学) 基质(化学分析) 材料科学 成体干细胞 细胞外基质 生物 免疫学 内皮干细胞 内分泌学 生物化学 生物技术 复合材料
作者
Wei Wei,Jipeng Li,Shuo Chen,Mingjiao Chen,Qing Xie,Hao Sun,Jing Ruan,Huifang Zhou,Xiaoping Bi,Ai Zhuang,Zhengwei You,Ping Gu,Xianqun Fan
出处
期刊:Journal of Materials Chemistry B [Royal Society of Chemistry]
卷期号:5 (13): 2468-2482 被引量:36
标识
DOI:10.1039/c6tb03150a
摘要

Tissue engineering technology that adopts mesenchymal stem cells combined with scaffolds presents a promising strategy for tissue regeneration. Human adipose-derived stem cells (hADSCs) have attracted considerable attention in bone engineering for their osteogenic potential. The extracellular matrix (ECM) is critical for the stem cell niche as a physical support and is known to be able to maintain stem cell properties. In this study, the ECM derived from ADSCs was produced and termed the ADM. The ADM was demonstrated to markedly promote proliferation of bone marrow derived stem cells (BMSCs) and exhibited strongly osteogenic simulative effects in vitro. The results showed that alkaline phosphatase (ALP) activity, Alizarin red S (ARS) staining, osteogenic gene markers and proteins were significantly up-regulated. Next, we developed a poly(sebacoyl diglyceride) (PSeD) mesh scaffold coated with the ADM and evaluated its capacity to create an osteogenic microenvironment. BMSCs were cultured on the composite scaffolds and subjected to osteogenic differentiation in vitro. The results showed that the composite scaffolds facilitated the osteogenesis more than a simple PSeD scaffold. Then the PSeD/ADM scaffold seeded with BMSCs was used to repair critical-sized calvarial defects in rats, which significantly enhanced the reparative effects as confirmed via micro-CT, sequential fluorescent labeling and histological observation. In conclusion, we demonstrated that the ADM could promote both proliferation and osteogenesis of BMSCs, and the combination of ADM and PSeD synergistically stimulated bone formation, which may provide a novel scheme for bone regeneration.

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