Role of WT1 in Ischaemic Angiogenesis
dc.contributor.advisor
Hadoke, Patrick
en
dc.contributor.advisor
Hastie, Nick
en
dc.contributor.author
Ogley, Robert James
en
dc.contributor.sponsor
other
en
dc.date.accessioned
2018-09-05T09:44:00Z
dc.date.available
2018-09-05T09:44:00Z
dc.date.issued
2018-11-30
dc.description.abstract
Ischaemia causes irreversible tissue damage in cardiovascular disease. Since
regenerative angiogenesis fails to consistently induce sufficient reperfusion to
facilitate repair, targeted manipulation of angiogenesis is clinically desirable.
The Wilms’ tumour suppressor (Wt1) is a transcription factor which regulates
numerous genes and cellular processes, including many intrinsic to
angiogenesis. We hypothesise that WT1 in the endothelium influences the
angiogenic function of endothelial cells.
WT1 was identified in endothelial and non-endothelial cells comprising vessel
outgrowths generated by cultured aortic rings from WT1-GFP reporter mice.
Inducible deletion of WT1 from the endothelium (VE-Wt1 KO) significantly
delayed angiogenesis in this assay (p<0.05 relative to controls).
In vivo, WT1 expression was evident in vascular endothelial and perivascular
cells of the hindlimb as early as 3 days following femoral artery ligation to
induce ischaemia, often in cells expressing epithelial and mesenchymal
markers simultaneously. However, VE-Wt1 KO had no effect on hindlimb
reperfusion (laser Doppler; days 0-28) or on vessel density (day 28). Similarly,
VE-Wt1 KO had no effect on vessel density or expression of angiogenic factors
(qRT-PCR) in sponges inserted subcutaneously in mice (20 days). To further
understand the role of WT1 in angiogenesis, transcriptomic RNA expression
analysis was performed in WT1+ and WT1- cells isolated (FACs) from sponges
after implantation in WT1-GFP mice. WT1+ cells exhibited higher expression
of genes involved in a number of processes relevant to tissue repair, including
angiogenesis (p=3.11x10-8), wound healing (p=3.45x10-7) and epithelial-to-mesenchymal
transition (EMT) (p=5.86x10-4).
These results shed new light on the role of WT1 in ischaemic angiogenesis. In
concurrence with previously published work, we show that deletion of
endothelial WT1 can delay angiogenesis however, WT1 is not just
instrumental in endothelial cells in this context. WT1 has a broader role in
tissue repair in ischaemia, in part through regulation of cell transition (EMT).
This work has improved our understanding of the regulatory role of WT1 in
angiogenesis and repair, while revealing a number of novel insights into the
function of WT1. This highlights WT1 as a potentially beneficial therapeutic
target to facilitate regeneration in cardiovascular disease.
en
dc.identifier.uri
http://hdl.handle.net/1842/31555
dc.language.iso
en
dc.publisher
The University of Edinburgh
en
dc.subject
angiogenesis
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dc.subject
Wilms’ tumour suppressor
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dc.subject
WT1
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dc.subject
transcription factors
en
dc.title
Role of WT1 in Ischaemic Angiogenesis
en
dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
Doctoral
en
dc.type.qualificationname
PhD Doctor of Philosophy
en
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