Edinburgh Research Archive

MMP-12 activity during vascular remodelling

dc.contributor.advisor
Hadoke, Patrick
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dc.contributor.advisor
Bradley, Mark
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dc.contributor.advisor
Dhaliwal, Kanwaldeep
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dc.contributor.author
Stott, Holly Rosannah
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dc.contributor.sponsor
other
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dc.date.accessioned
2017-10-05T10:02:19Z
dc.date.available
2017-10-05T10:02:19Z
dc.date.issued
2017-07-08
dc.description.abstract
Matrix metalloproteinases (MMPs) are required for tissue remodelling processes, including angiogenesis. MMP activity is generally proangiogenic but MMP-12 is suggested to be antiangiogenic and its precise role is still unclear. The work in this thesis describes the synthesis of an MMP-12 inhibitor and activity probe to address the hypothesis that MMP-12 inhibits angiogenesis. An inhibitor, synthesised in-house, selectively inhibited MMP-12 in in vitro recombinant enzyme assays. An activity probe, also synthesised in-house, was selective for MMP-12 in in vitro recombinant enzyme assays. The function of MMP-12 during angiogenesis was assessed using murine models of angiogenesis; the in vivo sponge implantation, and the ex vivo aortic ring assays. Angiogenesis and MMP activity were imaged in vivo in sponges in C57Bl6/J mice over 7 − 21 days (D) using commercial probes (MMPSense™ and AngioSense™). MMP-12 protein concentration and activity were higher in sponges during early angiogenesis (D 3 − 7) when gene expression of vascular endothelial growth factor (a proangiogenic marker) was also high. Gene expression for MMP-12 and platelet-derived growth factor receptor (a marker of vascular maturation) were both higher on D 21 as angiogenesis started to stabilise. The MMP-12 activity probe was unsuccessful in selectively detecting MMP-12 activity in sponge lysate mixtures from D 7 − 21. Administration of an MMP-12 inhibitor did not increase angiogenesis in the sponges in vivo. Additionally, sponges implanted in MMP-12-/- mice did not exhibit significant changes in angiogenesis or MMP activity when imaged in vivo using commercial probes (MMPSense™ and AngioSense™) on D 7. Supporting this, histological analysis of the sponges (removed on D 21) showed that deletion of MMP-12 also did not increase angiogenesis within the sponges.
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dc.identifier.uri
http://hdl.handle.net/1842/23609
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.subject
matrix metalloproteinases
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dc.subject
MMPs
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dc.subject
MMP-12 inhibitor
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dc.subject
angiogenesis
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dc.title
MMP-12 activity during vascular remodelling
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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