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丝素蛋白/明胶-硫酸软骨素-透明质酸可有效增强骨髓间充质干细胞的体外软骨生成。

Silk fibroin/gelatin-chondroitin sulfate-hyaluronic acid effectively enhances in vitro chondrogenesis of bone marrow mesenchymal stem cells.

作者信息

Sawatjui Nopporn, Damrongrungruang Teerasak, Leeanansaksiri Wilairat, Jearanaikoon Patcharee, Hongeng Suradej, Limpaiboon Temduang

机构信息

Biomedical Sciences, Graduate School, Khon Kaen University, Khon Kaen 40002, Thailand; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.

Department of Oral Diagnosis, Faculty of Dentistry, Khon Kaen University, Khon Kaen 40002, Thailand.

出版信息

Mater Sci Eng C Mater Biol Appl. 2015;52:90-6. doi: 10.1016/j.msec.2015.03.043. Epub 2015 Mar 24.

Abstract

Tissue engineering is becoming promising for cartilage repair due to the limited self-repair capacity of cartilage tissue. We previously fabricated and characterized a three-dimensional silk fibroin/gelatin-chondroitin sulfate-hyaluronic acid (SF-GCH) scaffold and showed that it could promote proliferation of human bone marrow mesenchymal stem cells (BM-MSCs). This study aimed to evaluate its biological performance as a new biomimetic material for chondrogenic induction of BM-MSCs in comparison to an SF scaffold and conventional pellet culture. We found that the SF-GCH scaffold significantly enhanced the proliferation and chondrogenic differentiation of BM-MSCs compared to the SF scaffold and pellet culture in which the production of sulfated glycoaminoglycan was increased in concordance with the up-regulation of chondrogenic-specific gene markers. Our findings indicate the significant role of SF-GCH by providing a supportive structure and the mimetic cartilage environment for chondrogenesis which enables cartilage regeneration. Thus, our fabricated SF-GCH scaffold may serve as a potential biomimetic material for cartilage tissue engineering.

摘要

由于软骨组织的自我修复能力有限,组织工程在软骨修复方面正变得很有前景。我们之前制备并表征了一种三维丝素蛋白/明胶-硫酸软骨素-透明质酸(SF-GCH)支架,并表明它能促进人骨髓间充质干细胞(BM-MSCs)的增殖。本研究旨在评估其作为一种新型仿生材料,与SF支架和传统微珠培养相比,在诱导BM-MSCs成软骨方面的生物学性能。我们发现,与SF支架和微珠培养相比,SF-GCH支架显著增强了BM-MSCs的增殖和成软骨分化,其中硫酸化糖胺聚糖的产生随着成软骨特异性基因标志物的上调而增加。我们的研究结果表明,SF-GCH通过提供支持结构和模拟软骨环境来促进软骨形成,从而发挥重要作用,实现软骨再生。因此,我们制备的SF-GCH支架可能成为软骨组织工程的一种潜在仿生材料。

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