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不同三维支架在体内软骨内骨生成中的性能。

Performance of different three-dimensional scaffolds for in vivo endochondral bone generation.

机构信息

Department of Biomaterials, Radboud University Medical Center, Dentistry 309, P.O. Box 9101, 6500 HB, Nijmegen, The

出版信息

Eur Cell Mater. 2014 Jun 10;27:350-64. doi: 10.22203/ecm.v027a25.

DOI:10.22203/ecm.v027a25
PMID:24913441
Abstract

In the context of skeletal tissue development and repair, endochondral ossification has inspired a new approach to regenerate bone tissue in vivo using a cartilage intermediate as an osteoinductive template. The aim of this study was to investigate the behavior of mesenchymal stem cells (MSCs) in regard to in vitro cartilage formation and in vivo bone regeneration when combined with different three-dimensional (3D) scaffold materials, i.e., hydroxyapatite/tricalcium phosphate (HA/TCP) composite block, polyurethane (PU) foam, poly(lactic-co-glycolic acid)/poly(ε-caprolactone) electrospun fibers (PLGA/PCL) and collagen I gel. To this end, rat MSCs were seeded on these scaffolds and chondrogenically differentiated in vitro for 4 weeks followed by in vivo subcutaneous implantation for 8 weeks. Nonetheless, the quality and maturity of in vivo ectopic bone formation appeared to be scaffold/material-dependent. Eight weeks of implantation was not sufficient to ossify the entire PLGA/PCL constructs, albeit a comprehensive remodeling of the cartilage had occurred. For HA/TCP, PU and collagen I scaffolds, more mature bone formation with rich vascularity and marrow stroma development could be observed. These data suggest that chondrogenic priming of MSCs in the presence of different scaffold materials allows the establishment of reliable templates for generating functional endochondral bone tissue in vivo without using osteoinductive growth factors. The morphology and maturity of bone formation.

摘要

在骨骼组织发育和修复的背景下,软骨内骨化激发了一种新的方法,即在体内使用软骨作为成骨诱导模板来再生骨组织。本研究旨在研究间充质干细胞(MSCs)在体外软骨形成和体内骨再生方面的行为,当与不同的三维(3D)支架材料结合时,即羟基磷灰石/磷酸三钙(HA/TCP)复合材料块、聚氨酯(PU)泡沫、聚(乳酸-共-乙醇酸)/聚(ε-己内酯)电纺纤维(PLGA/PCL)和胶原 I 凝胶。为此,将大鼠 MSCs 接种在这些支架上,并在体外进行 4 周的软骨分化,然后进行 8 周的皮下体内植入。然而,体内异位骨形成的质量和成熟似乎取决于支架/材料。8 周的植入不足以使整个 PLGA/PCL 结构骨化,尽管软骨已经全面重塑。对于 HA/TCP、PU 和胶原 I 支架,可以观察到更成熟的骨形成,具有丰富的血管和骨髓基质发育。这些数据表明,在不同支架材料存在的情况下,MSCs 的软骨前体细胞诱导允许在体内建立可靠的模板,用于生成功能性软骨内骨组织,而无需使用成骨诱导生长因子。骨形成的形态和成熟度。

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