Arslan Yavuz Emre, Sezgin Arslan Tugba, Derkus Burak, Emregul Emel, Emregul Kaan C
Regenerative Biomaterials Laboratory, Department of Bioengineering, Engineering Faculty, Canakkale Onsekiz Mart University, Canakkale 17100, Turkey.
Regenerative Biomaterials Laboratory, Department of Bioengineering, Engineering Faculty, Canakkale Onsekiz Mart University, Canakkale 17100, Turkey.
Colloids Surf B Biointerfaces. 2017 Jun 1;154:160-170. doi: 10.1016/j.colsurfb.2017.03.034. Epub 2017 Mar 18.
In the present study, we aimed at fabricating an osteoinductive biocomposite scaffold using keratin obtained from human hair, jellyfish collagen and eggshell-derived nano-sized spherical hydroxyapatite (nHA) for bone tissue engineering applications. Keratin, collagen and nHA were characterized with the modified Lowry method, free-sulfhydryl groups and hydroxyproline content analysis, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), attenuated total reflectance-fourier transform infrared spectroscopy (ATR-FTIR) and thermal gravimetric analysis (TGA) which confirmed the success of the extraction and/or isolation processes. Human adipose mesenchymal stem cells (hAMSCs) were isolated and the cell surface markers were characterized via flow cytometry analysis in addition to multilineage differentiation capacity. The undifferentiated hAMSCs were highly positive for CD29, CD44, CD73, CD90 and CD105, but were not seen to express hematopoietic cell surface markers such as CD14, CD34 and CD45. The cells were successfully directed towards osteogenic, chondrogenic and adipogenic lineages in vitro. The microarchitecture of the scaffolds and cell attachment were evaluated using scanning electron microscopy (SEM). The cell viability on the scaffolds was assessed by the MTT assay which revealed no evidence of cytotoxicity. The osteogenic differentiation of hAMSCs on the scaffolds was determined histologically using alizarin red S, osteopontin and osteonectin stainings. Early osteogenic differentiation markers of hAMSCs were significantly expressed on the collagen-keratin-nHA scaffolds. In conclusion, it is believed that collagen-keratin-nHA osteoinductive biocomposite scaffolds have the potential of being used in bone tissue engineering.
在本研究中,我们旨在制备一种骨诱导生物复合支架,该支架使用从人发中提取的角蛋白、水母胶原蛋白和蛋壳衍生的纳米级球形羟基磷灰石(nHA),用于骨组织工程应用。通过改良的洛里方法、游离巯基和羟脯氨酸含量分析、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)、衰减全反射傅里叶变换红外光谱(ATR-FTIR)和热重分析(TGA)对角蛋白、胶原蛋白和nHA进行了表征,证实了提取和/或分离过程的成功。分离出人脂肪间充质干细胞(hAMSCs),除多谱系分化能力外,还通过流式细胞术分析对细胞表面标志物进行了表征。未分化的hAMSCs对CD29、CD44、CD73、CD90和CD105呈高度阳性,但未观察到表达造血细胞表面标志物如CD14、CD34和CD45。这些细胞在体外成功地定向分化为成骨、成软骨和成脂谱系。使用扫描电子显微镜(SEM)评估了支架的微观结构和细胞附着情况。通过MTT法评估了支架上的细胞活力,结果显示没有细胞毒性的迹象。使用茜素红S、骨桥蛋白和骨连接蛋白染色,通过组织学方法确定了hAMSCs在支架上的成骨分化情况。hAMSCs的早期成骨分化标志物在胶原-角蛋白-nHA支架上显著表达。总之,据信胶原-角蛋白-nHA骨诱导生物复合支架具有用于骨组织工程的潜力。