Abstract

Cell structure depends on both matrix strain and stiffness, but their interactive effects are poorly understood. We investigated the interactive roles of matrix properties and stretching patterns on cell structure by uniaxially stretching U2OS cells expressing GFP-actin on silicone rubber sheets supporting either a surface-adsorbed coating or thick hydrogel of type-I collagen. Cells and their actin stress fibers oriented perpendicular to the direction of cyclic stretch on collagen-coated sheets, but oriented parallel to the stretch direction on collagen gels. There was significant alignment parallel to the direction of a steady increase in stretch for cells on collagen gels, while cells on collagen-coated sheets did not align in any direction. The extent of alignment was dependent on both strain rate and duration. Stretch-induced alignment on collagen gels was blocked by the myosin light-chain kinase inhibitor ML7, but not by the Rho-kinase inhibitor Y27632. We propose that active orientation of the actin cytoskeleton perpendicular and parallel to direction of stretch on stiff and soft substrates, respectively, are responses that tend to maintain intracellular tension at an optimal level. Further, our results indicate that cells can align along directions of matrix stress without collagen fibril alignment, indicating that matrix stress can directly regulate cell morphology.

Highlights

  • Cyclic stretching causes the alignment of several cell types perpendicular to the direction of stretch [1,2,3] with the extent of alignment dependent on stretch amplitude, frequency and spatial pattern [4,5,6]

  • We evaluated the effects of stretch on stress fibers (SFs) organization in nonconfluent U2OS cells adhered onto the top of collagen gels

  • We have previously shown that Rho-kinase and myosin light-chain kinase (MLCK) regulate different populations of SFs: peripheral SFs are sensitive to MLCK inhibition, while central SFs are sensitive to Rho-kinase inhibition [5]

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Summary

Introduction

Cyclic stretching causes the alignment of several cell types perpendicular to the direction of stretch [1,2,3] with the extent of alignment dependent on stretch amplitude, frequency and spatial pattern [4,5,6]. These experiments are generally performed with cells cultured on silicone rubber sheets coated with matrix proteins (typically collagen type-I or fibronectin). Inhibition of actomyosin contractility using inhibitors of the Rho GTPase and myosin light-chain kinase pathways suppress SF formation in the central and peripheral regions, respectively, with any remaining SFs orienting parallel to the stretch direction [5]

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