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利用人牙胚干细胞在大孔支架上进行软骨组织工程。

Cartilage tissue engineering on macroporous scaffolds using human tooth germ stem cells.

作者信息

Calikoglu Koyuncu A C, Gurel Pekozer G, Ramazanoglu M, Torun Kose G, Hasirci V

机构信息

Department of Genetics and Bioengineering, Yeditepe University, Istanbul, Turkey.

Department of Oral Surgery, Istanbul University, Istanbul, Turkey.

出版信息

J Tissue Eng Regen Med. 2017 Mar;11(3):765-777. doi: 10.1002/term.1975. Epub 2015 Jan 2.

Abstract

The main objective was to study cartilage regeneration through differentiation of human tooth germ stem cells (HTGSCs) into chondrocytes on different three-dimensional (3D) scaffolds (PCL, PLLA and PCL-PLLA). Scaffold topographies were studied by scanning electron microscopy and it was found that the scaffolds had interconnected macroporous structures. HTGSCs were isolated from impacted third molar tooth germs of young adult patients and grown for 3 weeks on the scaffolds in chondrogenic differentiation medium. Cell proliferation on the scaffolds was determined by MTS assay and it was observed that all scaffolds supported cell proliferation. Immunostaining was carried out for morphological and differentiation analyses. Immunohistochemical analyses revealed that the cells attached onto the scaffolds and deposited cartilage-specific extracellular matrix (ECM). Real-time PCR was performed to determine the expression levels of cartilage-specific genes. After 21 days of incubation in cartilage differentiation medium, expression of collagen type II increased only in the cells seeded onto PCL-PLLA blend scaffolds. Similarly, aggrecan expression was the highest on PCL-PLLA scaffolds after 3 weeks. These results suggest that all the scaffolds, and especially PCL-PLLA, were suitable for chondrogenic differentiation of HTGSCs. Copyright © 2015 John Wiley & Sons, Ltd.

摘要

主要目的是研究人牙胚干细胞(HTGSCs)在不同三维(3D)支架(聚己内酯、聚乳酸和聚己内酯 - 聚乳酸)上向软骨细胞分化以实现软骨再生。通过扫描电子显微镜研究支架拓扑结构,发现这些支架具有相互连接的大孔结构。从年轻成年患者的阻生第三磨牙牙胚中分离出HTGSCs,并在软骨分化培养基中的支架上培养3周。通过MTS测定法确定支架上的细胞增殖情况,观察到所有支架均支持细胞增殖。进行免疫染色以进行形态学和分化分析。免疫组织化学分析显示,细胞附着在支架上并沉积软骨特异性细胞外基质(ECM)。进行实时PCR以确定软骨特异性基因的表达水平。在软骨分化培养基中孵育21天后,仅接种在聚己内酯 - 聚乳酸混合支架上的细胞中II型胶原蛋白的表达增加。同样,3周后聚己内酯 - 聚乳酸支架上的聚集蛋白聚糖表达最高。这些结果表明,所有支架,尤其是聚己内酯 - 聚乳酸,都适合HTGSCs的软骨分化。版权所有©2015约翰威立父子有限公司。

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