Molecular-scale substrate anisotropy, crowding and division drive collective behaviours in cell monolayers

Author:

Luo Yimin12,Gu Mengyang3,Park Minwook4,Fang Xinyi3,Kwon Younghoon1,Urueña Juan Manuel5,Read de Alaniz Javier4,Helgeson Matthew E.2,Marchetti Cristina M.6,Valentine Megan T.1ORCID

Affiliation:

1. Department of Mechanical Engineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA

2. Department of Chemical Engineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA

3. Department of Statistics and Applied Probability, University of California, Santa Barbara, Santa Barbara, CA 93106, USA

4. Department of Chemistry and Biochemistry, University of California, Santa Barbara, Santa Barbara, CA 93106, USA

5. BioPACIFIC MIP, California NanoSystems Institute, Santa Barbara, CA 93106, USA

6. Department of Physics, University of California, Santa Barbara, Santa Barbara, CA 93106, USA

Abstract

The ability of cells to reorganize in response to external stimuli is important in areas ranging from morphogenesis to tissue engineering. While nematic order is common in biological tissues, it typically only extends to small regions of cells interacting via steric repulsion. On isotropic substrates, elongated cells can co-align due to steric effects, forming ordered but randomly oriented finite-size domains. However, we have discovered that flat substrates with nematic order can induce global nematic alignment of dense, spindle-like cells, thereby influencing cell organization and collective motion and driving alignment on the scale of the entire tissue. Remarkably, single cells are not sensitive to the substrate’s anisotropy. Rather, the emergence of global nematic order is a collective phenomenon that requires both steric effects and molecular-scale anisotropy of the substrate. To quantify the rich set of behaviours afforded by this system, we analyse velocity, positional and orientational correlations for several thousand cells over days. The establishment of global order is facilitated by enhanced cell division along the substrate’s nematic axis, and associated extensile stresses that restructure the cells’ actomyosin networks. Our work provides a new understanding of the dynamics of cellular remodelling and organization among weakly interacting cells.

Funder

University of California, Santa Barbara

Army Research Laboratory

Otis Williams Postdoctoral Fellowship

National Science Foundation

Hellman Family Foundation

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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