Abstract

Significant effort has gone towards parsing out the effects of surrounding microenvironment on macroscopic behavior of stem cells. Many of the microenvironmental cues, however, are intertwined, and thus, further studies are warranted to identify the intricate interplay among the conflicting downstream signaling pathways that ultimately guide a cell response. In this contribution, by patterning adhesive PEG (polyethylene glycol) hydrogels using Dip Pen Nanolithography (DPN), we demonstrate that substrate elasticity, subcellular elasticity, ligand density, and topography ultimately define mesenchymal stem cells (MSCs) spreading and shape. Physical characteristics are parsed individually with 7 kilopascal (kPa) hydrogel islands leading to smaller, spindle shaped cells and 105 kPa hydrogel islands leading to larger, polygonal cell shapes. In a parallel effort, a finite element model was constructed to characterize and confirm experimental findings and aid as a predictive tool in modeling cell microenvironments. Signaling pathway inhibition studies suggested that RhoA is a key regulator of cell response to the cooperative effect of the tunable substrate variables. These results are significant for the engineering of cell-extra cellular matrix interfaces and ultimately decoupling matrix bound cues presented to cells in a tissue microenvironment for regenerative medicine.

Highlights

  • Human mesenchymal stem cells are uniquely positioned as a highly promising cell source for tissue engineering and cell transplant strategies due to their unique capability of selfrenewal and capability to differentiate into many diverse cell types [1,2,3,4,5,6,7]

  • polydimethyl siloxane (PDMS) was spincoated onto cover slips at 500 rotations per minute (RPM) for 10 seconds followed by 2000 RPM for 60 seconds

  • poly(ethylene) glycol (PEG)-DA and PEG-SH mixture was chosen as hydrogel islands and by varying the concentration of PEG precursor, it was possible to more closely mimic the elasticity of tissue at the subcellular level

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Summary

Introduction

Human mesenchymal stem cells (hMSCs) are uniquely positioned as a highly promising cell source for tissue engineering and cell transplant strategies due to their unique capability of selfrenewal and capability to differentiate into many diverse cell types [1,2,3,4,5,6,7]. Cells are able to sense these variances through transmembrane proteins called integrin receptors that help govern cell-ECM signaling and link the cell to the proteins in the ECM [25,26,27,28,29] This cellECM interaction is crucial to sensing forces through tissue and the surroundings. More recent studies have uncovered that ECM topography can control cellular organization with the size and geometry of available surface area being able to alter cell shape, traction forces, and cell spreading [12,31,32,33,34,35,36,37,38]. Shown are the characteristics analyzed to determine cell behavior and spreading including cell size, focal adhesion distribution, cytoskeleton arrangement, and RhoA signaling pathway knockdowns. doi:10.1371/journal.pone.0081113.t001

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