Buckling without Bending: A New Paradigm in Morphogenesis

A curious feature of organ and organoid morphogenesis is that in certain cases, spatial oscillations in the thickness of the growing “film” are out of phase with the deformation of the slower-growing “substrate,” while in other cases, the oscillations are in phase. The former cannot be explained by...

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Main Authors: T. A. Engstrom, Teng Zhang, A. K. Lawton, A. L. Joyner, J. M. Schwarz
Format: Article
Language:English
Published: American Physical Society 2018-12-01
Series:Physical Review X
Online Access:http://doi.org/10.1103/PhysRevX.8.041053
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spelling doaj-f7c9aa598e40478fa3dc6db5b55d77dc2020-11-24T23:04:57ZengAmerican Physical SocietyPhysical Review X2160-33082018-12-018404105310.1103/PhysRevX.8.041053Buckling without Bending: A New Paradigm in MorphogenesisT. A. EngstromTeng ZhangA. K. LawtonA. L. JoynerJ. M. SchwarzA curious feature of organ and organoid morphogenesis is that in certain cases, spatial oscillations in the thickness of the growing “film” are out of phase with the deformation of the slower-growing “substrate,” while in other cases, the oscillations are in phase. The former cannot be explained by elastic bilayer instability, and contradict the notion that there is a universal mechanism by which brains, intestines, teeth, and other organs develop surface wrinkles and folds. Inspired by the microstructure of the embryonic cerebellum, we develop a new model of 2D morphogenesis in which system-spanning elastic fibers endow the organ with a preferred radius, while a separate fiber network resides in the otherwise fluidlike film at the outer edge of the organ and resists thickness gradients thereof. The tendency of the film to uniformly thicken or thin is described via a “growth potential.” Several features of cerebellum, +blebbistatin organoid, and retinal fovea morphogenesis, including out-of-phase behavior and a film thickness amplitude that is comparable to the radius amplitude, are readily explained by our simple analytical model, as may be an observed scale invariance in the number of folds in the cerebellum. We also study a nonlinear variant of the model, propose further biological and bioinspired applications, and address how our model is and is not unique to the developing nervous system.http://doi.org/10.1103/PhysRevX.8.041053
collection DOAJ
language English
format Article
sources DOAJ
author T. A. Engstrom
Teng Zhang
A. K. Lawton
A. L. Joyner
J. M. Schwarz
spellingShingle T. A. Engstrom
Teng Zhang
A. K. Lawton
A. L. Joyner
J. M. Schwarz
Buckling without Bending: A New Paradigm in Morphogenesis
Physical Review X
author_facet T. A. Engstrom
Teng Zhang
A. K. Lawton
A. L. Joyner
J. M. Schwarz
author_sort T. A. Engstrom
title Buckling without Bending: A New Paradigm in Morphogenesis
title_short Buckling without Bending: A New Paradigm in Morphogenesis
title_full Buckling without Bending: A New Paradigm in Morphogenesis
title_fullStr Buckling without Bending: A New Paradigm in Morphogenesis
title_full_unstemmed Buckling without Bending: A New Paradigm in Morphogenesis
title_sort buckling without bending: a new paradigm in morphogenesis
publisher American Physical Society
series Physical Review X
issn 2160-3308
publishDate 2018-12-01
description A curious feature of organ and organoid morphogenesis is that in certain cases, spatial oscillations in the thickness of the growing “film” are out of phase with the deformation of the slower-growing “substrate,” while in other cases, the oscillations are in phase. The former cannot be explained by elastic bilayer instability, and contradict the notion that there is a universal mechanism by which brains, intestines, teeth, and other organs develop surface wrinkles and folds. Inspired by the microstructure of the embryonic cerebellum, we develop a new model of 2D morphogenesis in which system-spanning elastic fibers endow the organ with a preferred radius, while a separate fiber network resides in the otherwise fluidlike film at the outer edge of the organ and resists thickness gradients thereof. The tendency of the film to uniformly thicken or thin is described via a “growth potential.” Several features of cerebellum, +blebbistatin organoid, and retinal fovea morphogenesis, including out-of-phase behavior and a film thickness amplitude that is comparable to the radius amplitude, are readily explained by our simple analytical model, as may be an observed scale invariance in the number of folds in the cerebellum. We also study a nonlinear variant of the model, propose further biological and bioinspired applications, and address how our model is and is not unique to the developing nervous system.
url http://doi.org/10.1103/PhysRevX.8.041053
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