Electrospun biomaterial scaffolds with varied topographies for neuronal differentiation of human induced pluripotent stem cells

Date

2014-12-30

Authors

Mohtaram, Nima Khadem
Ko, Junghyuk
King, Craig
Sun, Lin
Muller, Nathan
Jun, Martin Byung-Guk
Willerth, Stephanie

Journal Title

Journal ISSN

Volume Title

Publisher

Wiley

Abstract

In this study, we investigated the effect of micro and nanoscale scaffold topography on promoting neuronal differentiation of human induced pluripotent stem cells (iPSCs) and directing the resulting neuronal outgrowth in an organized manner. We used melt electrospinning to fabricate poly (ε-caprolactone) (PCL) scaffolds with loop mesh and biaxial aligned microscale topographies. Biaxial aligned microscale scaffolds were further functionalized with retinoic acid releasing PCL nanofibers using solution electrospinning. These scaffolds were then seeded with neural progenitors derived from human iPSCs. We found that smaller diameter loop mesh scaffolds (43.7 ± 3.9 μm) induced higher expression of the neural markers Nestin and Pax6 compared to thicker diameter loop mesh scaffolds (85 ± 4 μm). The loop mesh and biaxial aligned scaffolds guided the neurite outgrowth of human iPSCs along the topographical features with the maximum neurite length of these cells being longer on the biaxial aligned scaffolds. Finally, our novel bimodal scaffolds also supported the neuronal differentiation of human iPSCs as they presented both physical and chemical cues to these cells, encouraging their differentiation. These results give insight into how physical and chemical cues can be used to engineer neural tissue.

Description

Preprint article.

Keywords

human induced pluripotent stem cells, melt electrospinning, solution electrospinning, scaffold topography, neural tissue engineering

Citation

Mohtaram N.K. et al. (2015) Electrospun biomaterial scaffolds with varied topographies for neuronal differentiation of human induced pluripotent stem cells. Journal of Biomedical Materials Research. Part A. 103 (8) p.2591-2601.