PEER-REVIEWED PUBLICATION

2018

Role of boundary conditions in determining cell alignment in response to stretch

Chen K, Vigliotti A, et al.

Proceedings of the National Academy of Sciences of the United States of America (PNAS)

University of Virginia, University of Cambridge, Italian Aerospace Research Center, University of California - Santa Barbara

RESEARCH SUMMARY
This study investigated why many cell types align perpendicular to cyclic stretch on 2D membranes but often align parallel to stretch in 3D gels, explicitly testing the “strain avoidance” hypothesis that attributes 3D parallel alignment to avoidance of larger transverse compaction strains. Primary adult rat cardiac fibroblasts were embedded in collagen gels and cultured under systematically varied boundary conditions that independently controlled transverse compaction and restraint during static and cyclic stretching. The results showed that, under static or low-frequency conditions, fibroblast alignment correlated with the presence or absence of restraining boundary conditions rather than with the magnitude/pattern of transverse compaction: gels restrained in the loading direction produced strong alignment parallel to the restraint even when compaction was isotropic, while biaxially restrained gels produced low/random alignment. Cyclic stretch could drive perpendicular alignment in 3D, but only at substantially higher frequencies than typically required in 2D stretching studies. A modified stress-fiber thermodynamics/kinetics model incorporating traction boundary conditions and reduced strain transmission in soft gels reproduced the experimental findings across 3D conditions and matched published 2D frequency-dependent alignment trends, providing a unified mechanistic explanation for the apparent 2D vs 3D discrepancy.

CELLSCALE INSTRUMENT USED

MechanoCulture B1

Fibroblast-populated collagen gels were mechanically stimulated using CellScale MechanoCulture B1 devices, which convert programmed linear actuator motion into stretch of an inner 24-pin circular region within a media-filled “wet” chamber. Cruciform collagen gels were pinned to impose defined boundary conditions (uniaxial vs strip uniaxial with transverse restraint) and were subjected to static (0%) or cyclic stretch protocols, including 10% cyclic uniaxial stretch at 0.5 Hz for 24–72 h as well as higher-frequency cyclic stretch (2 Hz and 4 Hz) to probe frequency-dependent reorientation. The CellScale platform enabled controlled comparisons of alignment outcomes under x2 free-to-compact versus x2 constrained conditions, and supported time-course quantification of gel deformation/compaction (marker tracking) and cell alignment (F-actin imaging and orientation analysis) as a function of boundary condition and stretch frequency.
AUTHORS

Kellen Chen, Andrea Vigliotti, Mattia Bacca, Robert M. McMeeking, Vikram S. Deshpande, Jeffrey W. Holmes.

PUBLICATION DETAILS
JOURNAL

Proceedings of the National Academy of Sciences of the United States of America (PNAS)

YEAR

2018

INSTITUTIONS

University of Virginia, University of Cambridge, Italian Aerospace Research Center, University of California - Santa Barbara

COUNTRIES

Italy, United Kingdom, United States

INSTRUMENT USED

MechanoCulture B1

TESTING METHODS

Hydrated and Temperature Controlled TestingTensile Testing

RESEARCH APPLICATIONS

Cardiac Tissue Engineering & MechanicsECM & Decellularized Matrix MechanicsMechanotransduction

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