Surface tension determines tissue shape and growth kinetics

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Surface tension determines tissue shape and growth kinetics. / Ehrig, Sebastian; Schamberger, Barbara; Bidan, Cecile M et al.
In: Science Advances, Vol. 5.2019, No. 9, eaav9394, 11.09.2019.

Research output: Contribution to journalArticleResearchpeer-review

Harvard

Ehrig, S, Schamberger, B, Bidan, CM, West, A, Jacobi, C, Lam, K, Kollmannsberger, P, Petersen, A, Tomancak, P, Kommareddy, K, Fischer, F-D, Fratzl, P & Dunlop, JWC 2019, 'Surface tension determines tissue shape and growth kinetics', Science Advances, vol. 5.2019, no. 9, eaav9394. https://doi.org/10.1126/sciadv.aav9394

APA

Ehrig, S., Schamberger, B., Bidan, C. M., West, A., Jacobi, C., Lam, K., Kollmannsberger, P., Petersen, A., Tomancak, P., Kommareddy, K., Fischer, F.-D., Fratzl, P., & Dunlop, J. W. C. (2019). Surface tension determines tissue shape and growth kinetics. Science Advances, 5.2019(9), Article eaav9394. https://doi.org/10.1126/sciadv.aav9394

Vancouver

Ehrig S, Schamberger B, Bidan CM, West A, Jacobi C, Lam K et al. Surface tension determines tissue shape and growth kinetics. Science Advances. 2019 Sept 11;5.2019(9):eaav9394. doi: 10.1126/sciadv.aav9394

Author

Ehrig, Sebastian ; Schamberger, Barbara ; Bidan, Cecile M et al. / Surface tension determines tissue shape and growth kinetics. In: Science Advances. 2019 ; Vol. 5.2019, No. 9.

Bibtex - Download

@article{3b09c6b13eef409a855441601a873774,
title = "Surface tension determines tissue shape and growth kinetics",
abstract = "The collective self-organization of cells into three-dimensional structures can give rise to emergent physical properties such as fluid behavior. Here, we demonstrate that tissues growing on curved surfaces develop shapes with outer boundaries of constant mean curvature, similar to the energy minimizing forms of liquids wetting a surface. The amount of tissue formed depends on the shape of the substrate, with more tissue being deposited on highly concave surfaces, indicating a mechano-biological feedback mechanism. Inhibiting cell-contractility further revealed that active cellular forces are essential for generating sufficient surface stresses for the liquid-like behavior and growth of the tissue. This suggests that the mechanical signaling between cells and their physical environment, along with the continuous reorganization of cells and matrix is a key principle for the emergence of tissue shape.",
author = "Sebastian Ehrig and Barbara Schamberger and Bidan, {Cecile M} and A. West and C. Jacobi and K. Lam and P. Kollmannsberger and A. Petersen and P. Tomancak and K. Kommareddy and Franz-Dieter Fischer and P. Fratzl and Dunlop, {John W. C.}",
note = "Publisher Copyright: Copyright {\textcopyright} 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).",
year = "2019",
month = sep,
day = "11",
doi = "10.1126/sciadv.aav9394",
language = "English",
volume = "5.2019",
journal = "Science Advances",
issn = "2375-2548",
publisher = "American Association for the Advancement of Science",
number = "9",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Surface tension determines tissue shape and growth kinetics

AU - Ehrig, Sebastian

AU - Schamberger, Barbara

AU - Bidan, Cecile M

AU - West, A.

AU - Jacobi, C.

AU - Lam, K.

AU - Kollmannsberger, P.

AU - Petersen, A.

AU - Tomancak, P.

AU - Kommareddy, K.

AU - Fischer, Franz-Dieter

AU - Fratzl, P.

AU - Dunlop, John W. C.

N1 - Publisher Copyright: Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

PY - 2019/9/11

Y1 - 2019/9/11

N2 - The collective self-organization of cells into three-dimensional structures can give rise to emergent physical properties such as fluid behavior. Here, we demonstrate that tissues growing on curved surfaces develop shapes with outer boundaries of constant mean curvature, similar to the energy minimizing forms of liquids wetting a surface. The amount of tissue formed depends on the shape of the substrate, with more tissue being deposited on highly concave surfaces, indicating a mechano-biological feedback mechanism. Inhibiting cell-contractility further revealed that active cellular forces are essential for generating sufficient surface stresses for the liquid-like behavior and growth of the tissue. This suggests that the mechanical signaling between cells and their physical environment, along with the continuous reorganization of cells and matrix is a key principle for the emergence of tissue shape.

AB - The collective self-organization of cells into three-dimensional structures can give rise to emergent physical properties such as fluid behavior. Here, we demonstrate that tissues growing on curved surfaces develop shapes with outer boundaries of constant mean curvature, similar to the energy minimizing forms of liquids wetting a surface. The amount of tissue formed depends on the shape of the substrate, with more tissue being deposited on highly concave surfaces, indicating a mechano-biological feedback mechanism. Inhibiting cell-contractility further revealed that active cellular forces are essential for generating sufficient surface stresses for the liquid-like behavior and growth of the tissue. This suggests that the mechanical signaling between cells and their physical environment, along with the continuous reorganization of cells and matrix is a key principle for the emergence of tissue shape.

UR - http://www.scopus.com/inward/record.url?scp=85072403207&partnerID=8YFLogxK

U2 - 10.1126/sciadv.aav9394

DO - 10.1126/sciadv.aav9394

M3 - Article

VL - 5.2019

JO - Science Advances

JF - Science Advances

SN - 2375-2548

IS - 9

M1 - eaav9394

ER -