Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.527536
Title: Proteomic characterisation of vascular smooth muscle cells in atherosclerosis
Author: Full, Louise Elizabeth
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2010
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
During atherosclerosis, smooth muscle cells (SMC) migrate to the intima, losing their contractile ability and reacquiring characteristics seen during development: migration, proliferation, and synthesis of extracellular matrix – a process known as “phenotypic modulation”. I hypothesised that these phenotypic and functional characteristics indicate underlying differences in protein expression between intimal and medial SMC, which could constitute a characteristic signature indicative of the diseased state. I utilised 2-dimensional gel electrophoresis (2DE) and tandem mass spectrometry to compare the cytosolic proteome of the human SMC from atherosclerotic lesions with that of non-diseased SMC. Novel findings were validated by immunoblotting and immunohistochemistry. I detected decreases in contractile proteins and an increase in the oxidised form of peroxiredoxins in carotid atheroma-derived SMC - compared to non-diseased SMC. These changes indicate respectively loss of contractile features and exposure to oxidative stress, and are in accordance with the existing literature. I also identified significant decreases in the key mitochondrial proteins ATP synthase subunit-β and aldehyde dehydrogenase-2 potentially linked to mitochondrial damage. More notably, I described for the first time that differences in expression of members of the annexin family distinguish SMC derived from stable atheroma and unstable atheroma. The antiinflammatory protein Annexin I was significantly up regulated in SMC derived from stable plaques. Annexin II, a protein involved in facilitating fibrinolysis, was significantly down regulated in SMC derived from unstable plaques. These novel findings suggest that the failure of anti-inflammatory and antithrombotic mechanisms provided by SMC might play a role in plaque instability. Finally, I investigated the effect of the exposure to pro-atherogenic factors -cholesterol and the proinflammatory cytokine tumour necrosis factor α (TNFα) - on the proteome of SMC. With this, I was able to reproduce some of the features distinguishing atheroma-derived SMC, including the down regulation of contractile proteins and signs of mitochondrial damage. In addition I uncovered features of priming to challenge with TNFα in atheroma-derived SMC, potentially mediated by an increase of the p75 receptor. In contrast, cholesterol loading of SMC induced changes primarily in endoplasmic reticulum proteins, in line with current hypotheses in the literature of the activation of the Unfolded Protein Response – a protective mechanism engaged in conditions of endoplasmic reticulum stress. The proteome of SMC in advanced human atheroma has never been investigated before, particularly in the context of an unstable plaque. My data reveal an intricate relationship between inflammation, oxidative stress, mitochondrial damage and down regulation of mechanisms of resolution of inflammation in SMC in the context of vascular disease and its complications.
Supervisor: Monaco, Claudia ; Saklatvala, Jeremy ; Wait, Robin Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.527536  DOI: Not available
Share: