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Enhanced Differentiation of Human Embryonic Stem Cells Toward Definitive Endoderm on Ultrahigh Aspect Ratio Nanopillars

  • Camilla Holzmann Rasmussen
  • , Paul M. Reynolds
  • , Dorthe Roenn Petersen
  • , Mattias Hansson
  • , Robert M. McMeeking
  • , Martin Dufva
  • , Nikolaj Gadegaard*
  • *Corresponding author for this work
  • Technical University of Denmark
  • University of California at Santa Barbara
  • Novo Nordisk Foundation
  • University of Glasgow

Research output: Contribution to journalArticlepeer-review

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Abstract

Differentiation of human embryonic stem cells is widely studied as a potential unlimited source for cell replacement therapy to treat degenerative diseases such as diabetes. The directed differentiation of human embryonic stem cells relies mainly on soluble factors. Although, some studies have highlighted that the properties of the physical environment, such as substrate stiffness, affect cellular behavior. Here, mass-produced, injection molded polycarbonate nanopillars are presented, where the surface mechanical properties, i.e., stiffness, can be controlled by the geometric design of the ultrahigh aspect ratio nanopillars (stiffness can be reduced by 25.0003). It is found that tall nanopillars, yielding softer surfaces, significantly enhance the induction of definitive endoderm cells from pluripotent human embryonic stem cells, resulting in more consistent differentiation of a pure population compared to planar control. By contrast, further differentiation toward the pancreatic ­endoderm is less successful on “soft” pillars when compared to “stiff” pillars or control, indicating differential cues during the different stages of differentiation. To accompany the mechanical properties of the nanopillars, the concept of surface shear modulus is introduced to describe the characteristics of engineered elastic surfaces through micro or nanopatterning. This provides a framework whereby comparisons can be drawn between such materials and bulk elastomeric materials.

Original languageEnglish
Pages (from-to)815-823
Number of pages9
JournalAdvanced Functional Materials
Volume26
Issue number6
Early online date15 Dec 2015
DOIs
Publication statusPublished - 9 Feb 2016

Bibliographical note

Acknowledgements: C.H.R. and P.M.R. contributed equally to this work. The authors would like to thank the staff and technicians of the James Watt Nanofabrication Centre for their assistance during the substrate fabrication process – particularly Dr. Johnny Stormonth-Darling. C.H.R. and M.D. acknowledge financial support from Innovation Fund Denmark and Novo Nordisk A/S, Denmark. N.G. acknowledges funding from EPSRC (Engineering and Physical Sciences Research Council, BBSRC (Biotechnology and Biological Sciences Research Council), MRC (Medical Research Council), and the Royal Society. Further N.G. and P.M.R. acknowledge funding from the Engineering and Physical Sciences Research Council (EPSRC) Grant EP/F500424/1 DTC (Doctorial Training Centre) in Cell and Proteomic Technologies (PR), and EC-funded project NAPANIL (Contract No. FP7-CP-IP214249-2).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • human embryonic stem cells
  • injection moulding
  • mechanotransduction
  • nanostructures

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