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成骨培养基在 3D 培养中将人脂肪干细胞向成骨细胞分化方面优于生长因子。

Osteogenic medium is superior to growth factors in differentiation of human adipose stem cells towards bone-forming cells in 3D culture.

机构信息

Adult Stem Cells, Institute of Biomedical Technology, University of Tampere, Tampere, Finland.

出版信息

Eur Cell Mater. 2013 Jan 30;25:144-58. doi: 10.22203/ecm.v025a10.

DOI:10.22203/ecm.v025a10
PMID:23361609
Abstract

Human adipose stem cells (hASCs) have been recently used to treat bone defects in clinical practice. Yet there is a need for more optimal scaffolds and cost-effective approaches to induce osteogenic differentiation of hASCs. Therefore, we compared the efficiency of bone morphogenetic proteins (BMP-2 and BMP-7), vascular endothelial growth factor (VEGF), and osteogenic medium (OM) for the osteo-induction of hASCs in 3D culture. In addition, growth factors were tested in combination with OM. Commercially available bioactive glass scaffolds (BioRestore) and biphasic calcium phosphate granules (BoneCeramic) were evaluated as prospective carriers for hASCs. Both biomaterials supported hASC-viability, but BioRestore resulted in higher cell number than BoneCeramic, whereas BoneCeramic supported more significant collagen production. The most efficient osteo-induction was achieved with plain OM, promoting higher alkaline phosphatase activity and collagen production than growth factors. In fact, treatment with BMP-2 or VEGF did not increase osteogenic differentiation or cell number significantly more than maintenance medium with either biomaterial. Moreover, BMP-7 treatment consistently inhibited proliferation and osteogenic differentiation of hASCs. Interestingly, there was no benefit from growth factors added to OM. This is the first study to demonstrate that OM enhances hASC-differentiation towards bone-forming cells significantly more than growth factors in 3D culture.

摘要

人脂肪干细胞(hASCs)最近已在临床实践中用于治疗骨缺损。然而,需要更优化的支架和更具成本效益的方法来诱导 hASCs 的成骨分化。因此,我们比较了骨形态发生蛋白(BMP-2 和 BMP-7)、血管内皮生长因子(VEGF)和成骨培养基(OM)在 3D 培养中诱导 hASCs 成骨的效率。此外,还测试了生长因子与 OM 的联合使用。商业上可获得的生物活性玻璃支架(BioRestore)和双相磷酸钙颗粒(BoneCeramic)被评估为 hASCs 的潜在载体。这两种生物材料都支持 hASC 的存活,但 BioRestore 导致的细胞数量高于 BoneCeramic,而 BoneCeramic 则支持更多的胶原产生。普通 OM 实现了最有效的成骨诱导,其碱性磷酸酶活性和胶原产生均高于生长因子。事实上,与两种生物材料的维持培养基相比,BMP-2 或 VEGF 的治疗并没有显著增加成骨分化或细胞数量。此外,BMP-7 的治疗始终抑制 hASCs 的增殖和成骨分化。有趣的是,向 OM 中添加生长因子并没有带来益处。这是第一项研究表明,在 3D 培养中,OM 比生长因子更能显著增强 hASC 向成骨细胞的分化。

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