Alison E. Patteson: 0000-0002-4004-1734

Document Type



Summer 8-28-2019




National Institutes of Health, NSF Center for Engineering Mechanobiology, Fulbright Science and Technology Award, Prins Bernhard Cultuurfonds-Kuitse Fonds, National Science Center, Poland, Polish-American Fulbright Commission

Funding ID

NIH R01GM09697, NIH U54-CA193417, EB017753, NSF-DMR-1120901, CMMI-154857, NSF MRSEC/DMR-1720530 R01CA232256 and U01CA202177, UMO2017/26/D/ST4/00997


We acknowledge R. Wells and M. Perepelyuk for collection of rat blood, S. Diamond and R. Li for surplus blood products and D. Iwamoto for reading the manuscript. This work was supported by NIH R01GM09697, NIH U54-CA193417, EB017753 and NSF-DMR-1120901 (to P.A.J., L.C., A.E.P., K.P., K.C. and A.S.G.v.O.), by the NSF Center for Engineering Mechanobiology (CMMI-154857) through grants NSF MRSEC/DMR-1720530 R01CA232256 and U01CA202177 (X.C. and V.B.S.), by a Fulbright Science and Technology Award (A.S.G.v.O.) and by Prins Bernhard Cultuurfonds-Kuitse Fonds (A.S.G.v.O.). K.P. acknowledges partial support from the National Science Center, Poland under grant number UMO2017/26/D/ST4/00997 and from the Polish-American Fulbright Commission.

Official Citation

van Oosten, A.S.G., Chen, X., Chin, L. et al. Emergence of tissue-like mechanics from fibrous networks confined by close-packed cells. Nature 573, 96–101 (2019). https://doi.org/10.1038/s41586-019-1516-5




The viscoelasticity of the crosslinked semiflexible polymer networks—such as the internal cytoskeleton and the extracellular matrix—that provide shape and mechanical resistance against deformation is assumed to dominate tissue mechanics. However, the mechanical responses of soft tissues and semiflexible polymer gels differ in many respects. Tissues stiffen in compression but not in extension1,2,3,4,5, whereas semiflexible polymer networks soften in compression and stiffen in extension6,7. In shear deformation, semiflexible polymer gels stiffen with increasing strain, but tissues do not1,2,3,4,5,6,7,8. Here we use multiple experimental systems and a theoretical model to show that a combination of nonlinear polymer network elasticity and particle (cell) inclusions is essential to mimic tissue mechanics that cannot be reproduced by either biopolymer networks or colloidal particle systems alone. Tissue rheology emerges from an interplay between strain-stiffening polymer networks and volume-conserving cells within them. Polymer networks that soften in compression but stiffen in extension can be converted to materials that stiffen in compression but not in extension by including within the network either cells or inert particles to restrict the relaxation modes of the fibrous networks that surround them. Particle inclusions also suppress stiffening in shear deformation; when the particle volume fraction is low, they have little effect on the elasticity of the polymer networks. However, as the particles become more closely packed, the material switches from compression softening to compression stiffening. The emergence of an elastic response in these composite materials has implications for how tissue stiffness is altered in disease and can lead to cellular dysfunction9,10,11. Additionally, the findings could be used in the design of biomaterials with physiologically relevant mechanical properties.

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Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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