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In Vivo Ectopic Bone Formation by Devitalized Mineralized Stem Cell Carriers Produced Under Mineralizing Culture Condition

机译:在矿化培养条件下产生的失活矿化干细胞载体体内异位骨形成

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Functionalization of tissue engineering scaffolds with in vitro –generated bone-like extracellular matrix (ECM) represents an effective biomimetic approach to promote osteogenic differentiation of stem cells in vitro . However, the bone-forming capacity of these constructs (seeded with or without cells) is so far not apparent. In this study, we aimed at developing a mineralizing culture condition to biofunctionalize three-dimensional (3D) porous scaffolds with highly mineralized ECM in order to produce devitalized, osteoinductive mineralized carriers for human periosteal-derived progenitors (hPDCs). For this, three medium formulations [i.e., growth medium only (BM1), with ascorbic acid (BM2), and with ascorbic acid and dexamethasone (BM3)] supplemented with calcium (Ca2+) and phosphate (PO43?) ions simultaneously as mineralizing source were investigated. The results showed that, besides the significant impacts on enhancing cell proliferation (the highest in BM3 condition), the formulated mineralizing media differentially regulated the osteochondro-related gene markers in a medium-dependent manner (e.g., significant upregulation of BMP2 , bone sialoprotein, osteocalcin, and Wnt5a in BM2 condition). This has resulted in distinguished cell populations that were identifiable by specific gene signatures as demonstrated by the principle component analysis. Through devitalization, mineralized carriers with apatite crystal structures unique to each medium condition (by X-ray diffraction and SEM analysis) were obtained. Quantitatively, BM3 condition produced carriers with the highest mineral and collagen contents as well as human-specific VEGF proteins, followed by BM2 and BM1 conditions. Encouragingly, all mineralized carriers (after reseeded with hPDCs) induced bone formation after 8 weeks of subcutaneous implantation in nude mice models, with BM2-carriers inducing the highest bone volume, and the lowest in the BM3 condition (as quantitated by nano-computed tomography [nano-CT]). Histological analysis revealed different bone formation patterns, either bone ossicles containing bone marrow surrounding the scaffold struts (in BM2) or bone apposition directly on the struts' surface (in BM1 and BM3). In conclusion, we have presented experimental data on the feasibility to produce devitalized osteoinductive mineralized carriers by functionalizing 3D porous scaffolds with an in vitro cell-made mineralized matrix under the mineralizing culture conditions.
机译:具有体外生成的骨样细胞外基质(ECM)的组织工程支架的功能化是一种有效的仿生方法,可促进干细胞在体外的成骨分化。然而,到目前为止,这些构建体(接种或不接种细胞)的骨形成能力尚不明显。在这项研究中,我们旨在开发一种矿化培养条件,以利用高度矿化的ECM对三维(3D)多孔支架进行生物功能化,从而为人类骨膜来源的祖细胞(hPDC)生产失活的骨诱导矿化载体。为此,添加了钙(Ca 2 + )和磷酸盐的三种培养基配方[即仅生长培养基(BM1),抗坏血酸(BM2),抗坏血酸和地塞米松(BM3)]研究了同时作为矿化源的(PO 4 3?)离子。结果表明,除了对增强细胞增殖具有显着影响(在BM3条件下最高)外,配制的矿化培养基还以中等依赖的方式差异性调节骨软骨相关基因标记(例如BMP2,骨唾液蛋白,骨钙素和BM2条件下的Wnt5a)。如主要成分分析所证实的,这导致了可以通过特定基因特征识别的杰出细胞群。通过失活,获得了具有每种介质条件唯一的磷灰石晶体结构的矿化载体(通过X射线衍射和SEM分析)。从数量上讲,BM3条件产生的载体具有最高的矿物质和胶原蛋白含量以及人类特异性VEGF蛋白,其次是BM2和BM1条件。令人鼓舞的是,在裸鼠模型中,所有矿化的载体(与hPDC一起播种)在皮下植入8周后均诱导了骨形成,其中BM2载体诱导的骨骼体积最大,而BM3情况诱导的骨骼体积最低(通过纳米计算机断层扫描定量) [nano-CT])。组织学分析显示了不同的骨形成模式,要么是骨骼周围的骨听骨(在BM2中),要么是骨骼并列在支架表面(在BM1和BM3中)。总之,我们提供了关于在矿化培养条件下,通过体外细胞制备的矿化基质对3D多孔支架进行功能化来生产失活的骨诱导矿化载体的实验数据。

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