Back to Search
Start Over
Oxidative Stress Orchestrates Cell Polarity to Promote Embryonic Wound Healing
- Source :
- Developmental cell. 47(3)
- Publication Year :
- 2018
-
Abstract
- Summary Embryos have a striking ability to heal wounds rapidly and without scarring. Embryonic wound repair is a conserved process, driven by polarization of cell-cell junctions and the actomyosin cytoskeleton in the cells around the wound. However, the upstream signals that trigger cell polarization around wounds are unknown. We used quantitative in vivo microscopy in Drosophila and zebrafish embryos to identify reactive oxygen species (ROS) as a critical signal that orchestrates cell polarity around wounds. ROS promote trafficking of adherens junctions and accumulation of actin and myosin at the wound edge and are necessary for wound closure. We show that, in Drosophila, ROS drive wound healing in part through an ortholog of Src kinase, Src42A, which we identify as a redox sensor that promotes polarization of junctions and the cytoskeleton around wounds. We propose that ROS are a reparative signal that drives rapid embryonic wound healing in vertebrate and invertebrate species.
- Subjects :
- 0301 basic medicine
Embryo, Nonmammalian
Proto-Oncogene Proteins pp60(c-src)
Biology
Myosins
medicine.disease_cause
General Biochemistry, Genetics and Molecular Biology
Adherens junction
03 medical and health sciences
0302 clinical medicine
Myosin
Cell polarity
medicine
Animals
Drosophila Proteins
Cytoskeleton
Molecular Biology
Zebrafish
Wound Healing
integumentary system
Cell Polarity
Cell Biology
Actomyosin
Adherens Junctions
Cadherins
Embryonic stem cell
Actins
Cell biology
Oxidative Stress
030104 developmental biology
Drosophila melanogaster
Intercellular Junctions
Wound healing
Reactive Oxygen Species
030217 neurology & neurosurgery
Oxidative stress
Developmental Biology
Proto-oncogene tyrosine-protein kinase Src
Subjects
Details
- ISSN :
- 18781551
- Volume :
- 47
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Developmental cell
- Accession number :
- edsair.doi.dedup.....2ff048c8812b1b00b8980787e17b745d