| Literature DB >> 34405038 |
Shuang Zheng1, Qiong Liu1,2, Junhao He1, Xinlei Wang1, Kai Ye1, Xuan Wang1, Ce Yan1, Peng Liu1,3, Jiandong Ding1.
Abstract
Cell adhesion to extracellular matrices (ECM) is critical to physiological and pathological processes as well as biomedical and biotechnological applications. It has been known that a cell can adhere on an adhesive microisland only over a critical size. But no publication has concerned critical adhesion areas of cells on microislands with nanoarray decoration. Herein, we fabricated a series of micro-nanopatterns with different microisland sizes and arginine-glycine-aspartate (RGD) nanospacings on a nonfouling poly(ethylene glycol) background. Besides reproducing that nanospacing of RGD, a ligand of its receptor integrin (a membrane protein), significantly influences specific cell adhesion on bioactive nanoarrays, we confirmed that the concept of critical adhesion area originally suggested in studies of cells on micropatterns was justified also on the micro-nanopatterns, yet the latter exhibited more characteristic behaviors of cell adhesion. We found increased critical adhesion areas of human mesenchymal stem cells (hMSCs) on nanoarrayed microislands with increased RGD nanospacings. However, the numbers of nanodots with respect to the critical adhesion areas were not a constant. A unified interpretation was then put forward after combining nonspecific background adhesion and specific cell adhesion. We further carried out the asymptotic analysis of a series of micro-nanopatterned surfaces to obtain the effective RGD nanospacing on unpatterned free surfaces with densely grafted RGD, which could be estimated nonzero but has never been revealed previously without the assistance of the micro-nanopatterning techniques and the corresponding analysis. Electronic Supplementary Material: Supplementary materials and methods (details of fabrication of micro-nanopatterns), and supplementary results (selective adhesion or localization of hMSCs on nanoarrayed microislands with non-fouling background, calculation of critical number of integrin-ligand binding N*, etc.) are available in the online version of this article at 10.1007/s12274-021-3711-6. © Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021.Entities:
Keywords: arginine—glycine—aspartate (RGD) nanospacing; biomaterial; cell adhesion; critical adhesion area; poly(ethylene glycol); surface patterning
Year: 2021 PMID: 34405038 PMCID: PMC8359768 DOI: 10.1007/s12274-021-3711-6
Source DB: PubMed Journal: Nano Res ISSN: 1998-0000 Impact factor: 10.269