Functional immobilization of signaling proteins enables control of stem cell fate.

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • K. Alberti - , Leibniz Institute of Polymer Research Dresden (Author)
  • R. Davey - , University of Toronto (Author)
  • K. Onishi - , University of Toronto (Author)
  • S. George - , Mount Sinai Hospital (Toronto) (Author)
  • K. Salchert - , Leibniz Institute of Polymer Research Dresden (Author)
  • P. Seib - , Leibniz Institute of Polymer Research Dresden, University Hospital Carl Gustav Carus Dresden (Author)
  • Martin Bornhäuser - , Department of Internal Medicine I, Center for Regenerative Therapies Dresden (Author)
  • T. Pompe - , Leibniz Institute of Polymer Research Dresden (Author)
  • A. Nagy - , Mount Sinai Hospital (Toronto) (Author)
  • C. Werner - , Center for Regenerative Therapies Dresden, Leibniz Institute of Polymer Research Dresden, University of Toronto (Author)
  • P.W. Zandstra - , University of Toronto (Author)

Abstract

The mode of ligand presentation has a fundamental role in organizing cell fate throughout development. We report a rapid and simple approach for immobilizing signaling ligands to maleic anhydride copolymer thin-film coatings, enabling stable signaling ligand presentation at interfaces at defined concentrations. We demonstrate the utility of this platform technology using leukemia inhibitory factor (LIF) and stem cell factor (SCF). Immobilized LIF supported mouse embryonic stem cell (mESC) pluripotency for at least 2 weeks in the absence of added diffusible LIF. Immobilized LIF activated signal transducer and activator of transcription 3 (STAT3) and mitogen-activated protein kinase (MAPK) signaling in a dose-dependent manner. The introduced method allows for the robust investigation of cell fate responses from interface-immobilized ligands.

Details

Original languageEnglish
Pages (from-to)645-650
Number of pages6
JournalNature Methods
Volume5
Issue number7
Publication statusPublished - 2008
Peer-reviewedYes

External IDs

Scopus 46249111235
researchoutputwizard legacy.publication#24866
ORCID /0000-0003-0189-3448/work/162347615

Keywords