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胶原纳米纤维是用于人脂肪干细胞无血清成骨分化的仿生基质。

Collagen nanofibres are a biomimetic substrate for the serum-free osteogenic differentiation of human adipose stem cells.

作者信息

Sefcik Lauren S, Neal Rebekah A, Kaszuba Stephanie N, Parker Anna M, Katz Adam J, Ogle Roy C, Botchwey Edward A

机构信息

Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

J Tissue Eng Regen Med. 2008 Jun;2(4):210-20. doi: 10.1002/term.85.

Abstract

Electrospinning has recently gained widespread attention as a process capable of producing nanoscale fibres that mimic native extracellular matrix. In this study, we compared the osteogenic differentiation behaviour of human adipose stem cells (ASCs) on a 3D nanofibre matrix of type I rat tail collagen (RTC) and a 2D RTC collagen-coated substrate, using a novel serum-free osteogenic medium. The serum-free medium significantly enhanced the numbers of proliferating cells in culture, compared to ASCs in traditional basal medium containing 10% animal serum, highlighting a potential clinical role for in vitro stem cell expansion. Osteogenic differentiation behaviour was assessed at days 7, 14 and 21 using quantitative real-time RT-PCR analysis of the osteogenic genes collagen I (Coll I), alkaline phosphatase (ALP), osteopontin (OP), osteonectin (ON), osteocalcin (OC) and core-binding factor-alpha (cbfa1). All genes were upregulated (>one-fold) in ASCs cultured on nanofibre scaffolds over 2D collagen coatings by day 21. Synthesis of mineralized extracellular matrix on the scaffolds was assessed on day 21 with Alizarin red staining. These studies demonstrate that 3D nanoscale morphology plays a critical role in regulating cell fate processes and in vitro osteogenic differentiation of ASCs under serum-free conditions.

摘要

作为一种能够制造出模仿天然细胞外基质的纳米级纤维的工艺,静电纺丝最近受到了广泛关注。在本研究中,我们使用一种新型无血清成骨培养基,比较了人脂肪干细胞(ASC)在I型大鼠尾胶原(RTC)的3D纳米纤维基质和2D RTC胶原包被底物上的成骨分化行为。与在含有10%动物血清的传统基础培养基中的ASC相比,无血清培养基显著增加了培养中增殖细胞的数量,突出了其在体外干细胞扩增方面的潜在临床作用。在第7、14和21天,使用定量实时RT-PCR分析成骨基因I型胶原(Coll I)、碱性磷酸酶(ALP)、骨桥蛋白(OP)、骨连接蛋白(ON)、骨钙素(OC)和核心结合因子α(cbfa1)来评估成骨分化行为。到第21天,在纳米纤维支架上培养的ASC中,所有基因的表达均上调(>1倍),超过了2D胶原涂层上的表达。在第21天用茜素红染色评估支架上矿化细胞外基质的合成。这些研究表明,在无血清条件下,3D纳米级形态在调节细胞命运过程和ASC的体外成骨分化中起着关键作用。

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