Singh Milind, Berkland Cory, Detamore Michael S
Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045-7609, USA.
Tissue Eng Part B Rev. 2008 Dec;14(4):341-66. doi: 10.1089/ten.teb.2008.0304.
From embryonic development to wound repair, concentration gradients of bioactive signaling molecules guide tissue formation and regeneration. Moreover, gradients in cellular and extracellular architecture as well as in mechanical properties are readily apparent in native tissues. Perhaps tissue engineers can take a cue from nature in attempting to regenerate tissues by incorporating gradients into engineering design strategies. Indeed, gradient-based approaches are an emerging trend in tissue engineering, standing in contrast to traditional approaches of homogeneous delivery of cells and/or growth factors using isotropic scaffolds. Gradients in tissue engineering lie at the intersection of three major paradigms in the field-biomimetic, interfacial, and functional tissue engineering-by combining physical (via biomaterial design) and chemical (with growth/differentiation factors and cell adhesion molecules) signal delivery to achieve a continuous transition in both structure and function. This review consolidates several key methodologies to generate gradients, some of which have never been employed in a tissue engineering application, and discusses strategies for incorporating these methods into tissue engineering and implant design. A key finding of this review was that two-dimensional physicochemical gradient substrates, which serve as excellent high-throughput screening tools for optimizing desired biomaterial properties, can be enhanced in the future by transitioning from two dimensions to three dimensions, which would enable studies of cell-protein-biomaterial interactions in a more native tissue-like environment. In addition, biomimetic tissue regeneration via combined delivery of graded physical and chemical signals appears to be a promising strategy for the regeneration of heterogeneous tissues and tissue interfaces. In the future, in vivo applications will shed more light on the performance of gradient-based mechanical integrity and signal delivery strategies compared to traditional tissue engineering approaches.
从胚胎发育到伤口修复,生物活性信号分子的浓度梯度引导着组织的形成和再生。此外,细胞和细胞外结构以及力学特性的梯度在天然组织中也很明显。或许组织工程师在尝试通过将梯度纳入工程设计策略来再生组织时可以从自然中获得启示。事实上,基于梯度的方法是组织工程中一种新兴趋势,与使用各向同性支架均匀递送细胞和/或生长因子的传统方法形成对比。组织工程中的梯度处于该领域三个主要范式——仿生、界面和功能组织工程——的交叉点,通过结合物理(通过生物材料设计)和化学(与生长/分化因子及细胞粘附分子)信号传递来实现结构和功能的连续转变。本综述整合了几种生成梯度的关键方法,其中一些从未在组织工程应用中使用过,并讨论了将这些方法纳入组织工程和植入物设计的策略。本综述的一个关键发现是,二维物理化学梯度底物作为优化所需生物材料特性的出色高通量筛选工具,未来可通过从二维向三维转变来得到改进,这将能够在更接近天然组织的环境中研究细胞 - 蛋白质 - 生物材料相互作用。此外,通过分级物理和化学信号的联合递送进行仿生组织再生似乎是一种用于再生异质组织和组织界面的有前途的策略。未来,与传统组织工程方法相比,体内应用将更清楚地揭示基于梯度的机械完整性和信号传递策略的性能。