Centre for Cell Engineering, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.
Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, Scotland, UK.
Nat Mater. 2014 Jun;13(6):558-69. doi: 10.1038/nmat3980.
Stem cells respond to nanoscale surface features, with changes in cell growth and differentiation mediated by alterations in cell adhesion. The interaction of nanotopographical features with integrin receptors in the cells' focal adhesions alters how the cells adhere to materials surfaces, and defines cell fate through changes in both cell biochemistry and cell morphology. In this Review, we discuss how cell adhesions interact with nanotopography, and we provide insight as to how materials scientists can exploit these interactions to direct stem cell fate and to understand how the behaviour of stem cells in their niche can be controlled. We expect knowledge gained from the study of cell-nanotopography interactions to accelerate the development of next-generation stem cell culture materials and implant interfaces, and to fuel discovery of stem cell therapeutics to support regenerative therapies.
干细胞对纳米级表面特征做出响应,细胞生长和分化的变化是通过细胞黏附的改变来介导的。纳米形貌特征与细胞焦点黏附中的整合素受体相互作用改变了细胞与材料表面的黏附方式,并通过改变细胞生物化学和细胞形态来定义细胞命运。在这篇综述中,我们讨论了细胞黏附如何与纳米形貌相互作用,并深入了解材料科学家如何利用这些相互作用来指导干细胞命运,以及了解干细胞在其龛位中的行为如何得到控制。我们预计,从细胞-纳米形貌相互作用研究中获得的知识将加速下一代干细胞培养材料和植入界面的发展,并推动干细胞治疗的发现,以支持再生疗法。