Abstract

Self-organized patterning of mammalian embryonic stem cells on micropatterned surfaces has previously been established as an in vitro platform for early mammalian developmental studies, complimentary to in vivo studies. Traditional micropatterning methods, such as micro-contact printing (μCP), involve relatively complicated fabrication procedures, which restricts widespread adoption by biologists. Here, we demonstrate a rapid method of micropatterning by printing hydrogel micro-features onto a glass-bottomed culture vessel. The micro-features are printed using a projection stereolithography bioprinter yielding hydrogel structures that geometrically restrict the attachment of cells or proteins. Compared to traditional and physical photomasks, a digitally tunable virtual photomask is used in the projector to generate blue light patterns that enable rapid iteration with minimal cost and effort. We show that a protocol that makes use of this method together with LN521 coating, an extracellular matrix coating, creates a surface suitable for human embryonic stem cell (hESC) attachment and growth with minimal non-specific adhesion. We further demonstrate that self-patterning of hESCs following previously published gastrulation and ectodermal induction protocols achieves results comparable with those obtained with commercially available plates.

Highlights

  • Self-organized differentiation of embryonic stem cells on micropatterned surfaces has emerged as a valuable method for studying signaling and cell-fate patterning in early mammalian development

  • The PEGDA hydrogel was formed by free-radical polymerization of acrylate and methacrylate groups initiated by a blue light source (405 nm)

  • Our results with human embryonic stem cell (hESC) indicate the feasibility of performing developmental studies on these micropatterned surfaces

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Summary

Introduction

Self-organized differentiation of embryonic stem cells on micropatterned surfaces has emerged as a valuable method for studying signaling and cell-fate patterning in early mammalian development. In these protocols, ESCs are cultured on micropatterened substrates that geometrically confine cell colonies to be of a particular size and shape. ESCs are cultured on micropatterened substrates that geometrically confine cell colonies to be of a particular size and shape Treatment of these colonies with appropriately chosen courses of growth factor stimulation recapitulates aspects of embryonic patterning at gastrulation and neurulation stages.

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