Recapitulation of morphogenetic cell shape changes enables wound re-epithelialisation
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Wound repair is a fundamental, conserved mechanism for maintaining tissue homeostasis and shares many parallels with embryonic morphogenesis. Small wounds in simple epithelia rapidly assemble a contractile actomyosin cable at their leading edge, as well as dynamic filopodia that finally knit the wound edges together. Most studies of wound re-epithelialisation have focused on the actin machineries that assemble in the leading edge of front row cells and that resemble the contractile mechanisms that drive morphogenetic episodes, including Drosophila dorsal closure, but, clearly, multiple cell rows back must also contribute for efficient repair of the wound. Here, we examine the role of cells back from the wound edge and show that they also stretch towards the wound and cells anterior-posterior to the wound edge rearrange their junctions with neighbours to drive cell intercalation events. This process in anterior-posterior cells is active and dependent on pulses of actomyosin that lead to ratcheted shrinkage of junctions; the actomyosin pulses are targeted to breaks in the cell polarity protein Par3 at cell vertices. Inhibiting actomyosin dynamics back from the leading edge prevents junction shrinkage and inhibits the wound edge from advancing. These events recapitulate cell rearrangements that occur during germband extension, in which intercalation events drive the elongation of tissues.
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A recent Drosophila study showed active cell shape changes and junctional alterations several rows back from the wound edge, shifting attention from the front row of cells.
“A recent study in Drosophila showed that there are active cell shape changes and junctional alterations several rows back from the wound edge, moving attention away from the front row of cells, which have been considered the key players (121).”
From Wound repair and regeneration: Mechanisms, signaling, and translation (2014) · cites this paper as [121]
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Mortensen, R. D., Moore, R. P., Fogerson, S. M., Chiou, H. Y., Obinero, C. V., Prabhu, N. K., Wei, A. H., Crawford, J. M., & Kiehart, D. P. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200233 · Cited by 6 · see citing works
Turley, J., Chenchiah, I. V., Martin, P. B., Liverpool, T. B., & Weavers, H. (2023) · eLife · doi:10.7554/elife.87949.1 · Cited by 4 · see citing works
Self-citationGupta, K., Mukherjee, S., Sen, S., & Sonawane, M. S. (2022) · Development · doi:10.1242/dev.199363 · Cited by 3 · see citing works
Porfírio-Rodrigues, P., Pereira, T., Jacinto, A., & Carvalho, L. (2025) · Journal of Cell Science · doi:10.1242/jcs.263674 · Cited by 3 · see citing works
Turley, J., Chenchiah, I. V., Martin, P. B., Liverpool, T. B., & Weavers, H. (2024) · eLife · doi:10.7554/elife.87949.3 · Cited by 2 · see citing works
Self-citationInitiation of epithelial wound closure by an active instability at the purse string
Movrin, V., & Krajnc, M. (2024) · Biophysical Journal · doi:10.1016/j.bpj.2024.11.008 · Cited by 2 · see citing works
ReSCU-Nets: Recurrent U-Nets for segmentation of three-dimensional microscopy data
Hawkins, R., Balaghi, N., Rothenberg, K. E., Ly, M., & Fernández‐González, R. (2025) · The Journal of Cell Biology · doi:10.1083/jcb.202506102 · Cited by 3 · see citing works
Turley, J., Chenchiah, I. V., Martin, P. B., Liverpool, T. B., & Weavers, H. (2024) · eLife · doi:10.7554/elife.87949.2 · Cited by 2 · see citing works
Self-citationDynamics of Wound Closure in Living Nematic Epithelia
Andralojc, H., Turley, J., Weavers, H., Martin, P. B., Chenchiah, I. V., Bennett, R. R., & Liverpool, T. B. (2026) · Physical Review Letters · doi:10.1103/8871-8m6c · Cited by 1 · see citing works
Self-citationRecapitulation of morphogenetic cell shape changes enables wound re-epithelialisation
Razzell, W., Wood, W., & Martin, P. B. (2014) · Journal of Cell Science · doi:10.1242/jcs.154773 · Cited by 1 · see citing works
Self-citationMechanochemical modelling of dorsal closure reveals emergent cell behaviour in tissue morphogenesisPreprint
Atzeni, F., Pasakarnis, L., Mosca, G., Smith, R. S., Aegerter, C. M., & Brunner, D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.20.912725 · Cited by 1 · see citing works
Actomyosin Dynamics During Coordinated Cell Movements in Embryonic Wound Repair
Kobb, A. B. (2019) · TSpace (University of Toronto) · Cited by 1 · see citing works
Turley, J., Chenchiah, I. V., Martin, P. B., Liverpool, T. B., & Weavers, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.20.533343 · Cited by 1 · see citing works
Self-citationJunctional and cytoplasmatic contributions in wound healingPreprint
Mosaffa, P., Tetley, R. J., Ferran, A. R., Mao, Y., & Muñoz, J. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.21.959379
For Special Issue: Tissue size and shape
Mao, Y., & Franck Pichaud, N. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.05.019
Malamy, J. E., Sassaman, M., & Mony, M. P. (2026) · Molecular Biology of the Cell · doi:10.1091/mbc.e26-02-0094
- Authors
- Razzell, W., Wood, W., & Martin, P.
- Affiliations
- University of Bristol (GB)
- University of Bath (GB)
- Corresponding author
- Martin, Paul
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2014-05-01
- Volume
- 141
- Issue
- 9
- Pages
- 1814-1820
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC3994776
- OpenAlex
- W2163949267
- Cited by
- 82
- References
- 34
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 6 · 2023: 7 · 2022: 10 · 2021: 5 · 2020: 8 · 2019: 8 · 2018: 9 · 2017: 6 · 2016: 5 · 2015: 7 · 2014: 6
- FWCI
- 3.96
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Development (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Explore Bristol Research (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Wellcome Trust (090899)
- Medical Research Council (MR/J002577/1)
- National Institute of General Medical Sciences (R01GM084947)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- wound healing, cell intercalation, actomyosin contractility, Par3, cell polarity, morphogenesis, epithelial mechanics, filopodia, Drosophila
- MeSH terms
- Animals, Drosophila melanogaster, Embryo, Nonmammalian, Epithelium, Intercellular Junctions, Morphogenesis, Myosins, Wound Healing, Cell Polarity, Cell Shape
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