TY - JOUR
T1 - Computable early Caenorhabditis elegans embryo with a phase field model
AU - Kuang, Xiangyu
AU - Guan, Guoye
AU - Wong, Ming-Kin
AU - Chan, Lu-Yan
AU - Zhao, Zhongying
AU - Tang, Chao
AU - Zhang, Lei
N1 - Funding information:
LZ was supported by the National Key R&D Program of China 2021YFF1200500 and the National Natural Science Foundation of China 12050002. CT was supported by the National Natural Science Foundation of China 12090053 and 32088101. ZZ was supported by the Hong Kong Research Grants Council HKBU12100118, HKBU12100917, HKBU12123716 and the HKBU Interdisciplinary Research Cluster Fund.
Publisher Copyright:
© 2022 Kuang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2022/1/14
Y1 - 2022/1/14
N2 - Morphogenesis is a precise and robust dynamic process during metazoan embryogenesis, consisting of both cell proliferation and cell migration. Despite the fact that much is known about specific regulations at molecular level, how cell proliferation and migration together drive the morphogenesis at cellular and organismic levels is not well understood. Using Caenorhabditis elegans as the model animal, we present a phase field model to compute early embryonic morphogenesis within a confined eggshell. With physical information about cell division obtained from three-dimensional time-lapse cellular imaging experiments, the model can precisely reproduce the early morphogenesis process as seen in vivo, including time evolution of location and morphology of each cell. Furthermore, the model can be used to reveal key cell-cell attractions critical to the development of C. elegans embryo. Our work demonstrates how genetic programming and physical forces collaborate to drive morphogenesis and provides a predictive model to decipher the underlying mechanism.
AB - Morphogenesis is a precise and robust dynamic process during metazoan embryogenesis, consisting of both cell proliferation and cell migration. Despite the fact that much is known about specific regulations at molecular level, how cell proliferation and migration together drive the morphogenesis at cellular and organismic levels is not well understood. Using Caenorhabditis elegans as the model animal, we present a phase field model to compute early embryonic morphogenesis within a confined eggshell. With physical information about cell division obtained from three-dimensional time-lapse cellular imaging experiments, the model can precisely reproduce the early morphogenesis process as seen in vivo, including time evolution of location and morphology of each cell. Furthermore, the model can be used to reveal key cell-cell attractions critical to the development of C. elegans embryo. Our work demonstrates how genetic programming and physical forces collaborate to drive morphogenesis and provides a predictive model to decipher the underlying mechanism.
UR - http://www.scopus.com/inward/record.url?scp=85123320794&partnerID=8YFLogxK
U2 - 10.1371/journal.pcbi.1009755
DO - 10.1371/journal.pcbi.1009755
M3 - Journal article
SN - 1553-734X
VL - 18
JO - PLoS Computational Biology
JF - PLoS Computational Biology
IS - 1
M1 - e1009755
ER -