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Notch1–Dll4 signalling and mechanical force regulate leader cell formation during collective cell migration

Author

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  • Reza Riahi

    (The University of Arizona
    Present address: Harvard-MIT Health Sciences and Technology, Massachusetts Institute of Technology and Harvard Medical School, Cambridge, Massachusetts 02139, USA)

  • Jian Sun

    (The University of Arizona)

  • Shue Wang

    (The University of Arizona)

  • Min Long

    (Xinqiao Hospital, Third Military Medical University
    The University of Arizona)

  • Donna D. Zhang

    (The University of Arizona)

  • Pak Kin Wong

    (The University of Arizona)

Abstract

At the onset of collective cell migration, a subset of cells within an initially homogenous population acquires a distinct ‘leader’ phenotype with characteristic morphology and motility. However, the factors driving the leader cell formation as well as the mechanisms regulating leader cell density during the migration process remain to be determined. Here we use single-cell gene expression analysis and computational modelling to show that the leader cell identity is dynamically regulated by Dll4 signalling through both Notch1 and cellular stress in a migrating epithelium. Time-lapse microscopy reveals that Dll4 is induced in leader cells after the creation of the cell-free region and leader cells are regulated via Notch1–Dll4 lateral inhibition. Furthermore, mechanical stress inhibits Dll4 expression and leader cell formation in the monolayer. Collectively, our findings suggest that a reduction of mechanical force near the boundary promotes Notch1–Dll4 signalling to dynamically regulate the density of leader cells during collective cell migration.

Suggested Citation

  • Reza Riahi & Jian Sun & Shue Wang & Min Long & Donna D. Zhang & Pak Kin Wong, 2015. "Notch1–Dll4 signalling and mechanical force regulate leader cell formation during collective cell migration," Nature Communications, Nature, vol. 6(1), pages 1-11, May.
    • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7556
    DOI: 10.1038/ncomms7556
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