Investigation of the role of hepatic stellate cells in acute liver failure and hepatocarcinogenesis
dc.contributor.advisor
Henderson, Neil
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dc.contributor.advisor
Iredale, John
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dc.contributor.author
Thompson, Alexandra Inés
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dc.contributor.sponsor
other
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dc.date.accessioned
2018-03-22T15:05:53Z
dc.date.available
2018-03-22T15:05:53Z
dc.date.issued
2017-07-08
dc.description.abstract
Introduction: Hepatic stellate cells (HSC) and myofibroblasts may be relevant stromal
drivers of human hepatocellular carcinoma (HCC). It was hypothesised that targeted
inhibition of αv integrin-mediated TGF-β activation, by HSC or hepatocytes, may result
in reduced peri-tumoural and intra-tumoural extracellular matrix formation, and reduced
hepatic carcinogenesis.
The role of HSC in acute liver injury is less well characterised. It was anticipated that
integrin signalling on HSC and hepatocytes might also be relevant in the acute setting.
The emerging technique of intravital microscopy (IVM) allows detailed, real-time
investigation of the cellular processes involved in hepatocyte injury, cell death and repair.
It was hypothesised that this could be coupled with mouse models of HCC and acute
liver injury, to perform sequential imaging under anaesthesia.
Aims: (i) To determine the effect of targeted inhibition of αv integrins on HSC and
hepatocytes, during hepatocarcinogenesis, in a mouse model of HCC. (ii) To investigate
the effect of targeted inhibition of αv and other integrins on HSC, hepatocytes, and liver
sinusoidal endothelial cells (LSEC), during acute liver injury, in the mouse model of
paracetamol-induced liver injury. (iii) To develop IVM of the liver, via an abdominal
imaging window, with optimisation of surgical and imaging techniques, to allow
sequential imaging of the same animal.
Methods: The diethylnitrosamine (DEN)-induced mouse model of hepatocarcinogenesis
was used, and PDGFRβ-Cre;αvfl/fl and Alb-Cre;αvfl/fl mice were employed to deplete αv
integrins on HSC and hepatocytes respectively. Tumours were harvested at 40 weeks
post-DEN. Tumour size and number was evaluated in all animals.
PDGFRβ-Cre;αvfl/fl and Alb-Cre;αvfl/fl mice were used in the paracetamol model, to
investigate the role of αv integrins in acute liver injury. PDGFRβ-Cre;β8fl/fl and Alb-Cre;β
8fl/fl animals were also tested in this model. The role of integrins in liver sinusoidal
endothelial cells (LSEC) during paracetamol-induced liver injury was evaluated using
Cdh5-Cre mice.
IVM of the liver was performed by surgical implantation of an abdominal imaging window,
consisting of a titanium ring and coverslip, secured in place with a purse string suture.
Fluorescent reporter mice were used to identify hepatic and vascular architecture, and
other label-free microscope technologies were utilised to image collagen, lipid
distribution, necrotic areas and blood flow within tissues.
Results: In large cohorts of PDGFRβ-Cre;αvfl/fl, Alb-Cre;αvfl/fl, and control animals, there
was no difference in mean tumour size or number, at 40 weeks. Targeted inhibition of α
v integrins and β 8 integrin on hepatocytes, HSC or LSEC was not protective in
paracetamol-induced liver injury.
IVM of the liver can be performed on animals with HCC and throughout paracetamol-induced
liver injury, to obtain high quality, real-time images of multiple cell lineages and
the hepatic microenvironment.
Conclusions: The role of TGF-β in HCC pathogenesis is complex and context-dependent.
Targeted loss of αv integrin did not result in reduction in tumour burden in
this non-cirrhotic model of HCC. IVM of the liver is a powerful tool to quantify
inflammatory infiltrates and assessment of vascular remodelling throughout the course of acute liver injury and regeneration, providing insights into the biological processes
determining recovery.
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dc.identifier.uri
http://hdl.handle.net/1842/28936
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Thompson AI, Conroy KP, Henderson NC. Hepatic stellate cells: central modulators of hepatic carcinogenesis. BMC Gastroenterology. 2015: 15(63). PMID: 26489516.
en
dc.relation.hasversion
Vliegenthart AD, Shaffer JM, Clarke JI, Peeters LE, Caporali A, Bateman DN, Wood DM, Dargan PI, Craig DG, Moore JK, Thompson AI, Henderson NC, Webb DJ, Sharkey J, Antoine DJ, Park BK, Bailey MA, Lader E, Simpson KJ, Dear JW. Comprehensive microRNA profiling in acetaminophen toxicity identifies novel circulating biomarkers for human liver and kidney injury. Scientific Reports. 2015: 5 (15501). PMID:26013123.
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dc.subject
hepatocellular carcinoma
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dc.subject
hepatic stellate cell
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dc.subject
αv integrin
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dc.subject
hepatocytes
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dc.subject
stellate cells
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dc.subject
paracetamol poisoning
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dc.subject
mouse model
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dc.title
Investigation of the role of hepatic stellate cells in acute liver failure and hepatocarcinogenesis
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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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