Rutledge Katy, Jabbarzadeh Ehsan
Department of Chemical Engineering, University of South Carolina, Columbia, SC, 29208, USA.
Department of Chemical Engineering, University of South Carolina, Columbia, SC, 29208, USA; Biomedical Engineering Program, University of South Carolina, Columbia, SC, 29208, USA; Department of Orthopaedic Surgery, University of South Carolina School of Medicine, Columbia, SC, 29209, USA.
J Nanomed Nanotechnol. 2014 Aug;5(4). doi: 10.4172/2157-7439.1000217. Epub 2014 Aug 12.
Tissue engineering utilizes cells, signaling molecules, and scaffolds towards creating functional tissue to repair damaged organs. Pluripotent stem cells (PSCs) are a promising cell source due to their ability to self-renewal indefinitely and their potential to differentiate into almost any cell type. Great strides have been taken to parse the physiological mechanisms by which PSCs respond to their microenvironment and commit to a specific lineage. The combination of physical cues and chemical factors is thought to have the most profound influence on stem cell behavior, therefore a major focus of tissue engineering strategies is scaffold design to incorporate these signals. One overlooked component of the microenvironment researchers attempt to recapitulate with three dimensional (3D) substrates is the nanoarchitecture formed by the fibrillar network of extracellular matrix (ECM) proteins. These nanoscale features have the ability to impact cell adhesion, migration, proliferation, and lineage commitment. Significant advances have been made in deciphering how these nanoscale cues interact with stem cells to determine phenotype, but much is still unknown as to how the interplay between physical and chemical signals regulate and cellular fate. This review dives deeper to investigate nanoscale platforms for engineering tissue, as well use the use of these nanotechnologies to drive pluripotent stem cell lineage determination.
组织工程利用细胞、信号分子和支架来创建功能性组织以修复受损器官。多能干细胞(PSC)是一种很有前景的细胞来源,因为它们具有无限自我更新的能力以及分化为几乎任何细胞类型的潜力。在解析PSC对其微环境做出反应并定向分化为特定谱系的生理机制方面已经取得了很大进展。物理线索和化学因素的组合被认为对干细胞行为具有最深远的影响,因此组织工程策略的一个主要重点是设计能够整合这些信号的支架。研究人员试图用三维(3D)基质重现的微环境中一个被忽视的组成部分是由细胞外基质(ECM)蛋白的纤维网络形成的纳米结构。这些纳米级特征能够影响细胞黏附、迁移、增殖和谱系定向。在解读这些纳米级线索如何与干细胞相互作用以决定细胞表型方面已经取得了重大进展,但在物理和化学信号之间的相互作用如何调节细胞命运方面仍有许多未知之处。这篇综述更深入地探讨了用于组织工程的纳米级平台,以及利用这些纳米技术来驱动多能干细胞谱系定向。