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Title: PIEZO1 regulates leader cell formation and cellular coordination during collective keratinocyte migration
The collective migration of keratinocytes during wound healing requires both the generation and transmission of mechanical forces for individual cellular locomotion and the coordination of movement across cells. Leader cells along the wound edge transmit mechanical and biochemical cues to ensuing follower cells, ensuring their coordinated direction of migration across multiple cells. Despite the observed importance of mechanical cues in leader cell formation and in controlling coordinated directionality of cell migration, the underlying biophysical mechanisms remain elusive. The mechanically-activated ion channel PIEZO1 was recently identified to play an inhibitory role during the reepithelialization of wounds. Here, through an integrative experimental and mathematical modeling approach, we elucidate PIEZO1’s contributions to collective migration. Time-lapse microscopy reveals that PIEZO1 activity inhibits leader cell formation at the wound edge. To probe the relationship between PIEZO1 activity, leader cell formation and inhibition of reepithelialization, we developed an integrative 2D continuum model of wound closure that links observations at the single cell and collective cell migration scales. Through numerical simulations and subsequent experimental validation, we found that coordinated directionality plays a key role during wound closure and is inhibited by upregulated PIEZO1 activity. We propose that PIEZO1-mediated retraction suppresses leader cell formation which inhibits coordinated directionality between cells during collective migration.  more » « less
Award ID(s):
1763272 1953410
PAR ID:
10503813
Author(s) / Creator(s):
; ; ; ;
Editor(s):
Haugh, Jason M.
Publisher / Repository:
PLOS Computational Biology
Date Published:
Journal Name:
PLOS Computational Biology
Volume:
20
Issue:
4
ISSN:
1553-7358
Page Range / eLocation ID:
e1011855
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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