Clinical Engineering, UKCTE, UKBioTEC, LINSET, University of Liverpool, Duncan Building, Daulby Street, Liverpool L69 3GA, UK.
J Mater Sci Mater Med. 2010 Mar;21(3):1021-9. doi: 10.1007/s10856-009-3976-x.
The development of homogenously nano-patterned chemically modified surfaces that can be used to initiate a cellular response, particularly stem cell differentiation, in a highly controlled manner without the need for exogenous biological factors has never been reported, due to that fact that precisely defined and reproducible systems have not been available that can be used to study cell/material interactions and unlock the potential of a material driven cell response. Until now material driven stem cell (furthermore any cell) responses have been variable due to the limitations in definition and reproducibility of the underlying substrate and the lack of true homogeneity of modifications that can dictate a cellular response at a sub-micron level that can effectively control initial cell interactions of all cells that contact the surface. Here we report the successful design and use of homogenously molecularly nanopatterned surfaces to control initial stem cell adhesion and hence function. The highly specified nano-patterned arrays were compared directly to silane modified bulk coated substrates that have previously been proven to initiate mesenchymal stem cell (MSC) differentiation in a heterogenous manner, the aim of this study was to prove the efficiency of these previously observed cell responses could be enhanced by the incorporation of nano-patterns. Nano-patterned surfaces were prepared by Dip Pen Nanolithography (DPN) to produce arrays of 70 nm sized dots separated by defined spacings of 140, 280 and 1000 nm with terminal functionalities of carboxyl, amino, methyl and hydroxyl and used to control cell growth. These nanopatterned surfaces exhibited unprecedented control of initial cell interactions and will change the capabilities for stem cell definition in vitro and then cell based medical therapies. In addition to highlighting the ability of the materials to control stem cell functionality on an unprecedented scale this research also introduces the successful scale-up of DPN and the novel chemistries and systems to facilitate the production of homogeneously patterned substrates (5 mm2) that are applicable for use in in vitro cell conditions over prolonged periods for complete control of material driven cell responses.
尚未有报道称,已经开发出均质纳米图案化化学修饰表面,可用于在高度受控的情况下引发细胞反应,特别是干细胞分化,而无需外源性生物因素。这是因为以前没有可用的精确定义和可重复的系统来研究细胞/材料相互作用并释放材料驱动细胞反应的潜力。直到现在,由于基础底物的定义和可重复性以及修饰的真正均匀性的限制,材料驱动的干细胞(进一步说是任何细胞)反应一直具有变异性,这些限制可以在亚微米水平上决定细胞反应,可以有效地控制所有与表面接触的细胞的初始细胞相互作用。在这里,我们报告了成功设计和使用均质分子纳米图案化表面来控制初始干细胞粘附,从而控制其功能。高度特定的纳米图案阵列与以前已被证明以异质方式引发间充质干细胞(MSC)分化的硅烷修饰的大块涂层基底进行了直接比较,本研究的目的是证明通过掺入纳米图案可以提高这些先前观察到的细胞反应的效率。通过笔式纳米光刻(DPN)制备纳米图案表面,以产生由 70nm 大小的点组成的阵列,这些点之间的间隔分别为 140、280 和 1000nm,具有羧基、氨基、甲基和羟基等末端官能团,并用于控制细胞生长。这些纳米图案表面表现出对初始细胞相互作用的前所未有的控制能力,将改变体外干细胞定义的能力,然后是基于细胞的治疗方法。除了突出材料在前所未有的规模上控制干细胞功能的能力外,这项研究还介绍了 DPN 的成功扩展以及新的化学和系统,以促进同质图案化基底(5mm2)的生产,这些基底适用于体外细胞条件下延长时间的使用,以完全控制材料驱动的细胞反应。