PUBLICATION
Plexins function in epithelial repair in both Drosophila and zebrafish
- Authors
- Yoo, S.K., Pascoe, H.G., Pereira, T., Kondo, S., Jacinto, A., Zhang, X., Hariharan, I.K.
- ID
- ZDB-PUB-160728-27
- Date
- 2016
- Source
- Nature communications 7: 12282 (Journal)
- Registered Authors
- Keywords
- Adherens junctions, Disease model, Drosophila
- MeSH Terms
-
- Actins/metabolism
- Adherens Junctions/metabolism
- Animal Fins/metabolism
- Animals
- Cell Adhesion Molecules/metabolism*
- Drosophila melanogaster/metabolism*
- Epithelial Cells/metabolism
- Epithelium/metabolism*
- Nerve Tissue Proteins/metabolism*
- RNA Interference
- Signal Transduction
- Wound Healing*
- Zebrafish/metabolism*
- PubMed
- 27452696 Full text @ Nat. Commun.
Citation
Yoo, S.K., Pascoe, H.G., Pereira, T., Kondo, S., Jacinto, A., Zhang, X., Hariharan, I.K. (2016) Plexins function in epithelial repair in both Drosophila and zebrafish. Nature communications. 7:12282.
Abstract
In most multicellular organisms, homeostasis is contingent upon maintaining epithelial integrity. When unanticipated insults breach epithelial barriers, dormant programmes of tissue repair are immediately activated. However, many of the mechanisms that repair damaged epithelia remain poorly characterized. Here we describe a role for Plexin A (PlexA), a protein with particularly well-characterized roles in axonal pathfinding, in the healing of damaged epithelia in Drosophila. Semaphorins, which are PlexA ligands, also regulate tissue repair. We show that Drosophila PlexA has GAP activity for the Rap1 GTPase, which is known to regulate the stability of adherens junctions. Our observations suggest that the inhibition of Rap1 activity by PlexA in damaged Drosophila epithelia allows epithelial remodelling, thus facilitating wound repair. We also demonstrate a role for Plexin A1, a zebrafish orthologue of Drosophila PlexA, in epithelial repair in zebrafish tail fins. Thus, plexins function in epithelial wound healing in diverse taxa.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping