Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan; Cardiovascular Surgery, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
J Biomed Mater Res A. 2013 Oct;101(10):2808-16. doi: 10.1002/jbm.a.34589. Epub 2013 Mar 5.
The aim of this study was to investigate the ability of nano-sized collagen I molecules (nanoparticles or nanofibrils) and a 5-azacytidine (5-aza) treatment to enhance the differentiation of rat mesenchymal stem cells (MSCs) toward a cardiomyogenic phenotype in vitro. Second passaged MSCs were cocultured with nano-sized collagen I molecules for 24 h and then treated with 10 μM 5-aza for 24 h. The results demonstrated that the size of the cells increased significantly and acquired a flattened, triangular-shaped morphology after treatment with nano-sized collagen I molecules and 5-aza. The cells are connecting with adjoining cells by forming myotube-like structures. Additional treatment of the MSCs with nano-sized collagen I fibrils significantly increased two transcription factors GATA-4 (12.6-fold increase) and Nkx2.5 (4.8-fold increase) expressions compared with MSC groups treated only with 5-aza at 3-day culturing. Furthermore, MSCs pretreated with nano-sized collagen fibrils significantly increased the expressions of cardiac genes of troponin I, β-myosin heavy chain, and cardiac α-actin compared with MSC groups treated only with 5-aza (all, p < 0.01 or better). These results indicate that culturing MSCs with nano-sized collagen I molecules, which may act as scaffolds or soluble protein ingredients, leads to alterations in gene expression and affects the differentiation fate induced with 5-aza.
本研究旨在探讨纳米级 I 型胶原分子(纳米颗粒或纳米原纤维)和 5-氮杂胞苷(5-aza)处理对体外诱导大鼠间充质干细胞(MSCs)向心肌表型分化能力的影响。第二代 MSCs 与纳米级 I 型胶原分子共培养 24 小时,然后用 10 μM 5-aza 处理 24 小时。结果表明,细胞体积明显增大,经纳米级 I 型胶原和 5-aza 处理后呈扁平、三角形形态。细胞通过形成肌管样结构与相邻细胞相连。与仅用 5-aza 处理的 MSC 组相比,在用纳米级胶原纤维进一步处理 MSCs 时,转录因子 GATA-4(增加 12.6 倍)和 Nkx2.5(增加 4.8 倍)的表达显著增加,在 3 天培养时。此外,与仅用 5-aza 处理的 MSC 组相比,用纳米级胶原纤维预处理的 MSCs 心肌肌钙蛋白 I、β-肌球蛋白重链和心脏α-肌动蛋白的心脏基因表达显著增加(均 P<0.01 或更好)。这些结果表明,用纳米级 I 型胶原分子培养 MSCs,可能作为支架或可溶性蛋白成分,导致基因表达的改变,并影响 5-aza 诱导的分化命运。