TY - JOUR
T1 - Differential cell adhesion implemented by Drosophila Toll corrects local distortions of the anterior-posterior compartment boundary
AU - Iijima, Norihiro
AU - Sato, Katsuhiko
AU - Kuranaga, Erina
AU - Umetsu, Daiki
N1 - Funding Information:
We thank Yang Hong, Yoshimasa Yagi, Christian Dahmann, Shigeo Hayashi, David Strutt, the NIG-FLY Stock Center, and the Bloomington Drosophila Stock Center; Yu-Chiun Wang and Shigeo Hayashi for critical comments on the paper; Shu Kondo for providing a vector for CRISPR/Cas9-mediated knock-in DNA construction; and the Kuranaga lab members for useful discussion. This work is supported by JST CREST Japan to E.K., the research grant for Astellas Foundation for Research on Metabolic Disorders to E.K., Global Station for Soft Matter at Hokkaido University to K.S., Grants-in-Aid for Scientific Research from MEXT to K.S. (17H02939), E.K. (JP26114003, JP16H04800, and JP24687027) and D.U. (15K18536, 17K07402, and 17H02939).
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12
Y1 - 2020/12
N2 - Maintaining lineage restriction boundaries in proliferating tissues is vital to animal development. A long-standing thermodynamics theory, the differential adhesion hypothesis, attributes cell sorting phenomena to differentially expressed adhesion molecules. However, the contribution of the differential adhesion system during tissue morphogenesis has been unsubstantiated despite substantial theoretical support. Here, we report that Toll-1, a transmembrane receptor protein, acts as a differentially expressed adhesion molecule that straightens the fluctuating anteroposterior compartment boundary in the abdominal epidermal epithelium of the Drosophila pupa. Toll-1 is expressed across the entire posterior compartment under the control of the selector gene engrailed and displays a sharp expression boundary that coincides with the compartment boundary. Toll-1 corrects local distortions of the boundary in the absence of cable-like Myosin II enrichment along the boundary. The reinforced adhesion of homotypic cell contacts, together with pulsed cell contraction, achieves a biased vertex sliding action by resisting the separation of homotypic cell contacts in boundary cells. This work reveals a self-organizing system that integrates a differential adhesion system with pulsed contraction of cells to maintain lineage restriction boundaries.
AB - Maintaining lineage restriction boundaries in proliferating tissues is vital to animal development. A long-standing thermodynamics theory, the differential adhesion hypothesis, attributes cell sorting phenomena to differentially expressed adhesion molecules. However, the contribution of the differential adhesion system during tissue morphogenesis has been unsubstantiated despite substantial theoretical support. Here, we report that Toll-1, a transmembrane receptor protein, acts as a differentially expressed adhesion molecule that straightens the fluctuating anteroposterior compartment boundary in the abdominal epidermal epithelium of the Drosophila pupa. Toll-1 is expressed across the entire posterior compartment under the control of the selector gene engrailed and displays a sharp expression boundary that coincides with the compartment boundary. Toll-1 corrects local distortions of the boundary in the absence of cable-like Myosin II enrichment along the boundary. The reinforced adhesion of homotypic cell contacts, together with pulsed cell contraction, achieves a biased vertex sliding action by resisting the separation of homotypic cell contacts in boundary cells. This work reveals a self-organizing system that integrates a differential adhesion system with pulsed contraction of cells to maintain lineage restriction boundaries.
UR - http://www.scopus.com/inward/record.url?scp=85097388269&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85097388269&partnerID=8YFLogxK
U2 - 10.1038/s41467-020-20118-y
DO - 10.1038/s41467-020-20118-y
M3 - Article
C2 - 33303753
AN - SCOPUS:85097388269
SN - 2041-1723
VL - 11
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6320
ER -