Long-lived engineering of glycans to direct stem cell fate

Angew Chem Int Ed Engl. 2015 Jan 26;54(5):1466-70. doi: 10.1002/anie.201409258. Epub 2014 Dec 4.

Abstract

Glycans mediate many critical, long-term biological processes, such as stem cell differentiation. However, few methods are available for the sustained remodeling of cells with specific glycan structures. A new strategy that enables the long-lived presentation of defined glycosaminoglycans on cell surfaces using HaloTag proteins (HTPs) as anchors is reported. By controlling the sulfation patterns of heparan sulfate (HS) on pluripotent embryonic stem cell (ESC) membranes, it is demonstrated that specific glycans cause ESCs to undergo accelerated exit from self-renewal and differentiation into neuronal cell types. Thus, the stable display of glycans on HTP scaffolds provides a powerful, versatile means to direct key signaling events and biological outcomes such as stem cell fate.

Keywords: cell signaling; embryonic stem cells; glycosaminoglycans; heparan sulfate; stem cell differentiation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Line
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism*
  • Fibroblast Growth Factor 2 / genetics
  • Fibroblast Growth Factor 2 / metabolism
  • Glycosaminoglycans / chemistry
  • Glycosaminoglycans / metabolism*
  • Heparitin Sulfate / chemistry
  • Heparitin Sulfate / metabolism
  • Mice
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Neurons / cytology
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics
  • Receptor, Fibroblast Growth Factor, Type 1 / metabolism
  • Signal Transduction
  • Transcription Factors / metabolism

Substances

  • Glycosaminoglycans
  • Transcription Factors
  • Fibroblast Growth Factor 2
  • Heparitin Sulfate
  • Receptor, Fibroblast Growth Factor, Type 1
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3