Yim Evelyn K F, Pang Stella W, Leong Kam W
Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Exp Cell Res. 2007 May 15;313(9):1820-9. doi: 10.1016/j.yexcr.2007.02.031. Epub 2007 Mar 12.
Human mesenchymal stem cells (hMSCs) have been shown to trans-differentiate into neuronal-like cells by culture in neuronal induction media, although the mechanism is not well understood. Topography can also influence cellular responses including enhanced differentiation of progenitor cells. As extracellular matrix (ECM) in vivo comprises topography in the nanoscale, we hypothesize that nanotopography could influence stem cell differentiation into specific non-default pathways, such as transdifferentiation of hMSCs. Differentiation and proliferation of hMSCs were studied on nanogratings of 350 nm width. Cytoskeleton and nuclei of hMSCs were aligned and elongated along the nanogratings. Gene profiling and immunostaining showed significant up-regulation of neuronal markers such as microtubule-associated protein 2 (MAP2) compared to unpatterned and micropatterned controls. The combination of nanotopography and biochemical cues such as retinoic acid further enhanced the up-regulation of neuronal marker expressions, but nanotopography showed a stronger effect compared to retinoic acid alone on unpatterned surface. This study demonstrated the significance of nanotopography in directing differentiation of adult stem cells.
人骨髓间充质干细胞(hMSCs)已被证明通过在神经元诱导培养基中培养可转分化为神经元样细胞,尽管其机制尚未完全了解。拓扑结构也可影响细胞反应,包括增强祖细胞的分化。由于体内细胞外基质(ECM)包含纳米级的拓扑结构,我们推测纳米拓扑结构可能会影响干细胞向特定非默认途径的分化,例如hMSCs的转分化。我们研究了宽度为350 nm的纳米光栅上hMSCs的分化和增殖。hMSCs的细胞骨架和细胞核沿纳米光栅排列并拉长。基因谱分析和免疫染色显示,与未图案化和微图案化对照相比,神经元标记物如微管相关蛋白2(MAP2)显著上调。纳米拓扑结构与视黄酸等生化信号的组合进一步增强了神经元标记物表达的上调,但与单独使用视黄酸相比,纳米拓扑结构在未图案化表面上显示出更强的作用。这项研究证明了纳米拓扑结构在指导成体干细胞分化中的重要性。