Center for Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Nanotechnology. 2011 May 27;22(21):212001. doi: 10.1088/0957-4484/22/21/212001. Epub 2011 Mar 31.
Cells interact with the surrounding environment by making tens to hundreds of thousands of nanoscale interactions with extracellular signals and features. The goal of nanoscale tissue engineering is to harness these interactions through nanoscale biomaterials engineering in order to study and direct cellular behavior. Here, we review two- and three-dimensional (2- and 3D) nanoscale tissue engineering technologies, and provide a holistic overview of the field. Techniques that can control the average spacing and clustering of cell adhesion ligands are well established and have been highly successful in describing cell adhesion and migration in 2D. Extension of these engineering tools to 3D biomaterials has created many new hydrogel and nanofiber scaffold technologies that are being used to design in vitro experiments with more physiologically relevant conditions. Researchers are beginning to study complex cell functions in 3D. However, there is a need for biomaterials systems that provide fine control over the nanoscale presentation of bioactive ligands in 3D. Additionally, there is a need for 2- and 3D techniques that can control the nanoscale presentation of multiple bioactive ligands and that can control the temporal changes in the cellular microenvironment.
细胞通过与细胞外信号和特征进行数万至数十万纳米级的相互作用来与周围环境相互作用。纳米级组织工程的目标是通过纳米级生物材料工程利用这些相互作用,以便研究和指导细胞行为。在这里,我们回顾了二维和三维(2D 和 3D)纳米级组织工程技术,并提供了该领域的全面概述。可以控制细胞黏附配体平均间隔和聚集的技术已经成熟,并在描述 2D 中的细胞黏附和迁移方面取得了巨大成功。这些工程工具在 3D 生物材料中的扩展已经创造了许多新的水凝胶和纳米纤维支架技术,这些技术正在被用于设计具有更生理相关条件的体外实验。研究人员开始在 3D 中研究复杂的细胞功能。然而,需要有生物材料系统来精细控制 3D 中生物活性配体的纳米级呈现。此外,还需要能够控制多个生物活性配体的纳米级呈现并能够控制细胞微环境的时间变化的 2D 和 3D 技术。