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首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Investigation of the optimal timing for chondrogenic priming of MSCs to enhance osteogenic differentiation in vitro as a bone tissue engineering strategy
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Investigation of the optimal timing for chondrogenic priming of MSCs to enhance osteogenic differentiation in vitro as a bone tissue engineering strategy

机译:作为骨组织工程策略,研究MSC软骨激发引发的最佳时机以增强体外成骨分化

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Recent in vitro tissue engineering approaches have shown that chondrogenic priming of human bone marrow mesenchymal stem cells (MSCs) can have a positive effect on osteogenesis in vivo. However, whether chondrogenic priming is an effective in vitro bone regeneration strategy is not yet known. In particular, the appropriate timing for chondrogenic priming in vitro is unknown albeit that in vivo cartilage formation persists for a specific period before bone formation. The objective of this study is to determine the optimum time for chondrogenic priming of MSCs to enhance osteogenic differentiation by MSCs in vitro. Pellets derived from murine and human MSCs were cultured in six different media groups: two control groups (chondrogenic and osteogenic) and four chondrogenic priming groups (10, 14, 21 and 28days priming). Biochemical analyses (Hoechst, sulfate glycosaminoglycan (sGAG), Alkaline Phosphate (ALP), calcium), histology (Alcian Blue, Alizarin Red) and immunohistochemistry (collagen types I, II and X) were performed on the samples at specific times. Our results show that after 49days the highest amount of sGAG production occurred in MSCs chondrogenically primed for 21days and 28days. Moreover we found that chondrogenic priming of MSCs in vitro for specific amounts of time (14days, 21days) can have optimum influence on their mineralization capacity and can produce a construct that is mineralized throughout the core. Determining the optimum time for chondrogenic priming to enhance osteogenic differentiation in vitro provides information that might lead to a novel regenerative treatment for large bone defects, as well as addressing the major limitation of core degradation and construct failure. Copyright (c) 2013 John Wiley & Sons, Ltd.
机译:最近的体外组织工程方法表明,人骨髓间充质干细胞(MSC)的软骨形成引发可对体内成骨产生积极影响。然而,软骨激发是否是一种有效的体外骨再生策略尚不清楚。特别是,尽管在骨形成之前体内软骨形成持续了特定的时间,但体外软骨激发的合适时机仍是未知的。这项研究的目的是确定MSC的软骨致敏增强体外MSC成骨分化的最佳时间。在六个不同的培养基组中培养源自鼠和人MSC的药丸:两个对照组(成软骨和成骨)和四个成软骨的引发组(引发10、14、21和28天)。在特定时间对样品进行生化分析(Hoechst,硫酸糖胺聚糖(sGAG),碱性磷酸酶(ALP),钙),组织学(Alcian Blue,茜素红)和免疫组织化学(I,II和X型胶原)。我们的结果表明,在经过49天的软骨生成刺激后的21天和28天,sGAG产量最高。此外,我们发现,在特定时间段(14天,21天)中,体外对MSC进行软骨激发可对其成矿能力产生最佳影响,并且可以产生在整个岩心中成矿的构造。确定软骨形成引发的最佳时间以增强体外成骨性分化提供的信息可能会导致针对大骨缺损的新型再生治疗,并解决核心降解和构建失败的主要局限性。版权所有(c)2013 John Wiley&Sons,Ltd.

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