Issue 1, 2016

Regulating the stemness of mesenchymal stem cells by tuning micropattern features

Abstract

There is increasing evidence that microstructures play an important role in the maintenance of the multipotency of stem cells. However, it is not clear how micropatterns affect the stemness of stem cells. We prepared micropatterns of different sizes, shapes and aspect ratios and used them for the culture of mesenchymal stem cells (MSCs) derived from human bone marrow to investigate their influence on the stemness of MSCs at the single cell level. The percentage of cells positively stained by stem cell markers decreased with increasing spreading area and aspect ratio. However, the cellular geometry controlled by the geometrical micropatterns had no significant influence on the expression of stem cell markers. The change in the stemness of stem cells was accompanied by changes in the nuclear activity and cytoskeleton. The nuclear activity increased with increasing spreading area and aspect ratio. The actin filament structure was significantly influenced by the spreading area and aspect ratio. The cells became stiffer when they had sufficient area to spread into or when they were elongated. These results suggest that controlling the cell morphology by micropatterns may be useful in varying the stemness of MSCs. This study will contribute to the design of materials for maintaining the multipotency of stem cells, enhancing their clinical application and helping to reveal the processes taking place under conditions of stem cell quiescence in vivo.

Graphical abstract: Regulating the stemness of mesenchymal stem cells by tuning micropattern features

Supplementary files

Article information

Article type
Paper
Submitted
23 Okt. 2015
Accepted
12 Nov. 2015
First published
12 Nov. 2015

J. Mater. Chem. B, 2016,4, 37-45

Author version available

Regulating the stemness of mesenchymal stem cells by tuning micropattern features

X. Wang, T. Nakamoto, I. Dulińska-Molak, N. Kawazoe and G. Chen, J. Mater. Chem. B, 2016, 4, 37 DOI: 10.1039/C5TB02215K

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