Rahimi Maryam, Mohseni-Kouchesfehani Homa, Zarnani Amir-Hassan, Mobini Sahba, Nikoo Shohreh, Kazemnejad Somaieh
Department of Animal Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
Nanobiotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran Immunology Research Center, Iran University of Medical Sciences, Tehran, Iran.
J Biomater Appl. 2014 Aug;29(2):199-208. doi: 10.1177/0885328213519835. Epub 2014 Jan 19.
Recently, silk fibroin scaffolds have been introduced as novel and promising biomaterials in the field of cardiac tissue engineering. This study was designed to compare infiltration, proliferation, and cardiac differentiation potential of menstrual blood-derived stem cells (MenSCs) versus bone marrow-derived mesenchymal stem cells (BMSCs) in Bombyx mori-derived silk scaffold. Our primary data revealed that the fabricated scaffold has mechanical and physical qualities suitable for cardiac tissue engineering. The MenSCs tracking in scaffolds using immunofluorescent staining and scanning electron microscopy confirmed MenSCs attachment, penetration, and distribution within the porous scaffold matrix. Based on proliferation assay using propidium iodide DNA quantification, the significantly higher level of growth rates of both MenSCs and BMSCs was documented in scaffolds than that in two-dimensional culture (p < 0.01). The expression level of TNNT2, a bona fide cardiac differentiation marker, in BMSCs differentiated on silk scaffolds was markedly higher than those cultured in two-dimensional culture indicating the improvement of cardiac differentiation in the silk scaffolds. Furthermore, differentiated MenSCs exhibited higher expression of TNNT2 compared with induced BMSCs. It seems that silk scaffold-seeded MenSCs could be viewed as a novel, safe, natural, and accessible construct for cardiac tissue engineering.
最近,丝素蛋白支架作为心脏组织工程领域中新型且有前景的生物材料被引入。本研究旨在比较月经血源性干细胞(MenSCs)与骨髓间充质干细胞(BMSCs)在家蚕衍生的丝支架中的浸润、增殖及心脏分化潜能。我们的原始数据显示,制备的支架具有适合心脏组织工程的机械和物理性质。使用免疫荧光染色和扫描电子显微镜对支架中的MenSCs进行追踪,证实了MenSCs在多孔支架基质内的附着、渗透和分布。基于使用碘化丙啶DNA定量的增殖分析,记录到支架中MenSCs和BMSCs的生长速率均显著高于二维培养中的生长速率(p < 0.01)。在丝支架上分化的BMSCs中,真正的心脏分化标志物TNNT2的表达水平明显高于二维培养中的表达水平,表明丝支架中心脏分化有所改善。此外,与诱导的BMSCs相比,分化的MenSCs表现出更高的TNNT2表达。似乎接种了MenSCs的丝支架可被视为心脏组织工程的一种新型、安全、天然且易于获取的构建物。