Supracellular Actomyosin Mediates Cell-Cell Communication and Shapes Collective Migratory Morphology

During collective cell migration, front cells tend to extend a predominant leading protrusion, which is rarely present in cells at the side or rear positions. Using Drosophila border cells (BCs) as a model system of collective migration, we revealed the presence of a supracellular actomyosin network...

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Veröffentlicht in:iScience 2020-06, Vol.23 (6), p.101204-101204, Article 101204
Hauptverfasser: Wang, Heng, Guo, Xuan, Wang, Xianping, Wang, Xiaobo, Chen, Jiong
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Sprache:eng
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Zusammenfassung:During collective cell migration, front cells tend to extend a predominant leading protrusion, which is rarely present in cells at the side or rear positions. Using Drosophila border cells (BCs) as a model system of collective migration, we revealed the presence of a supracellular actomyosin network at the peripheral surface of BC clusters. We demonstrated that the Myosin II-mediated mechanical tension as exerted by this peripheral supracellular network not only mediated cell-cell communication between leading BC and non-leading BCs but also restrained formation of prominent protrusions at non-leading BCs. Further analysis revealed that a cytoplasmic dendritic actin network that depends on the function of Arp2/3 complex interacted with the actomyosin network. Together, our data suggest that the outward pushing or protrusive force as generated from Arp2/3-dependent actin polymerization and the inward restraining force as produced from the supracellular actomyosin network together determine the collective and polarized morphology of migratory BCs. [Display omitted] •A supracellular actomyosin network encompasses the surface of migratory BC cluster•The network mediates cell-cell communication and restrains protrusion formation•Dynamics of myosin patches correlate with protrusion behaviors•A cytoplasmic dendritic actin population interacts with the actomyosin network Biological Sciences; Cell Biology; Organizational Aspects of Cell Biology; Functional Aspects of Cell Biology
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2020.101204