TY - JOUR
T1 - Wave propagation of junctional remodeling in collective cell movement of epithelial tissue
T2 - Numerical simulation study
AU - Hiraiwa, Tetsuya
AU - Kuranaga, Erina
AU - Shibata, Tatsuo
N1 - Funding Information:
This work was supported by MEXT KAKENHI Grant Number JP26114003 (EK), and the JSPS KAKENHI, grant numbers JP16K17777 (TH), JP24687027 (EK), JP16H04800 (EK), JP15KT0086 (TS).
Publisher Copyright:
© 2017 Hiraiwa, Kuranaga and Shibata.
PY - 2017/7/19
Y1 - 2017/7/19
N2 - During animal development, epithelial cells forming a monolayer sheet move collectively to achieve the morphogenesis of epithelial tissues. One driving mechanism of such collective cell movement is junctional remodeling, which is found in the process of clockwise rotation of Drosophila male terminalia during metamorphosis. However, it still remains unknown how the motions of cells are spatiotemporally organized for collective movement by this mechanism. Since these moving cells undergo elastic deformations, the influence of junctional remodeling may mechanically propagate among them, leading to spatiotemporal pattern formations. Here, using a numerical cellular vertex model, we found that the junctional remodeling in collective cell movement exhibits spatiotemporal self-organization without requiring spatial patterns of molecular signaling activity. The junctional remodeling propagates as a wave in a specific direction with a much faster speed than that of cell movement. Such propagation occurs in both the absence and presence of fluctuations in the contraction of cell boundaries.
AB - During animal development, epithelial cells forming a monolayer sheet move collectively to achieve the morphogenesis of epithelial tissues. One driving mechanism of such collective cell movement is junctional remodeling, which is found in the process of clockwise rotation of Drosophila male terminalia during metamorphosis. However, it still remains unknown how the motions of cells are spatiotemporally organized for collective movement by this mechanism. Since these moving cells undergo elastic deformations, the influence of junctional remodeling may mechanically propagate among them, leading to spatiotemporal pattern formations. Here, using a numerical cellular vertex model, we found that the junctional remodeling in collective cell movement exhibits spatiotemporal self-organization without requiring spatial patterns of molecular signaling activity. The junctional remodeling propagates as a wave in a specific direction with a much faster speed than that of cell movement. Such propagation occurs in both the absence and presence of fluctuations in the contraction of cell boundaries.
KW - Cell intercalation
KW - Collective cell migration
KW - Epithelial cells
KW - Mathematical model
KW - Mechanobiology
KW - Vertex model
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U2 - 10.3389/fcell.2017.00066
DO - 10.3389/fcell.2017.00066
M3 - Article
AN - SCOPUS:85026821486
SN - 2296-634X
VL - 5
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
IS - JUL
M1 - 66
ER -