Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.690373
Title: Coordinating cell-cell contacts with cell-matrix contacts in fibroblast migration during wound healing
Author: Brooks, Rebecca
Awarding Body: University of Bristol
Current Institution: University of Bristol
Date of Award: 2016
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Abstract:
Following injury, fibroblasts migrate into the wound bed, where they play essential roles in effective wound healing through matrix deposition and contraction. Fibroblast migration relies on cell-matrix and cell-cell contacts, both of which are regulated by transmembrane receptors that are differentially regulated during wound healing. The fibronectin receptor syndecan-4 is increased upon wounding, which promotes fibroblast migration through activation of small GTPases and the recycling of integrin a5~1. Members of the Eph family of receptor tyrosine kinases, which regulate cellcell contacts, are also differentially regulated upon wounding. Little is known about whether there is a relationship between the syndecan-4 and Eph receptors, and how this might regulate the balance between cell -cell and cell-matrix contacts, and therefore fibroblast migration and clustering. Using transient knockdown and genetic knockout models, this project demonstrates that syndecan-4 downregulates EphA2, a receptor that mediates cell-cell repulsion, through a PKCa- and Fyn-dependent mechanism. In syndecan-4 knockout mouse embryonic fibroblasts, elevated EphA2 expression increases sensitivity to the EphA2 ligand ephrinA 1 and increases the rate and frequency of cell-cell repulsion when compared to wild type, demonstrating that the relationship between syndecan-4 and EphA2 has a direct effect on fibroblast clustering. Importantly, the findings are translated in vivo; EphA2 expression is increased in syndecan-4 knockout mouse wounds compared to wild type. This may contribute to the healing defect previously observed in syndecan-4 knockout mice 1. We hypothesise that the balance between syndecan-4 and EphA2 signalling regulates the switch between fibroblast clustering or scattering, and therefore coordinates the initiation and resolution of healing.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.690373  DOI: Not available
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