Browse DORAS
Browse Theses
Search
Latest Additions
Creative Commons License
Except where otherwise noted, content on this site is licensed for use under a:

The role of altered cyclic strain patterns on proliferation and apoptosis of vascular smooth muscle cells - implications for in-stent restenosis

Colombo, Alberto (2009) The role of altered cyclic strain patterns on proliferation and apoptosis of vascular smooth muscle cells - implications for in-stent restenosis. PhD thesis, Dublin City University.

Full text available as:

[img]
Preview
PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
12Mb

Abstract

Currently, Percutaneous Transluminal Coronary Angioplasty (PTCA) followed by stent implantation is the frontline treatment in the management of coronary artery disease. To-date the main drawback of stent implantation is in-stent restenosis. Restenosis is a partial re-occlusion of the arterial wall predominantly due to vascular smooth muscle cells (SMC) migration from the media to the intima and subsequent SMC proliferation. A stent procedure dramatically alters the level of strains and stresses in the coronary artery and hence the mechanical environment of the SMC. We hypothesised that there exists a direct causal relationship between the level of strain and vascular SMC proliferation and apoptosis within the vessel wall. Cyclic strain can be seen as made by different independent components: mean strain, amplitude and frequency. In this work, the role of each strain component (mean strain, amplitude and frequency) in controlling Bovine Aortic Smooth Muscle Cells (BASMC) proliferative and apoptotic capacity was investigated. Cyclic strain decreased SMC proliferation and increased apoptosis in a temporal manner. The mean cyclic strain had no significant effect on the proliferative and apoptotic behaviour of SMC whereas SMC behaviour was highly dependent on strain amplitude. This observation was further validated using human SMC. The role of mean strain and strain amplitude was further investigated using a novel in-house phantom mock arterial system where BASMC were cultured inside a perfused stented Sylgard mock artery under physiological levels of strain. Vascular SMC proliferation was significantly increased (+40%) and apoptosis decreased within the stented region in comparison to the more compliant upstream and downstream non-stented regions of the mock Sylgard artery. We therefore conclude that the decrease in strain amplitude experienced by vascular SMC within the stented region may be responsible for SMC accumulation due to enhanced proliferation and decreased apoptosis. This study provides important evidence for the use of more compliant stent designs to maintain the anti-proliferative effect of cyclic strain on vascular SMC and therefore reduce restenosis.

Item Type:Thesis (PhD)
Date of Award:November 2009
Refereed:No
Supervisor(s):Lally, Caitriona and Cahill, Paul
Uncontrolled Keywords:stenting; biomechanics; smooth muscle cells; restenosis;
Subjects:Engineering > Mechanical engineering
Biological Sciences > Cell biology
Medical Sciences > Biomechanics
DCU Faculties and Centres:DCU Faculties and Schools > Faculty of Engineering and Computing > School of Mechanical and Manufacturing Engineering
Use License:This item is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 License. View License
Funders:Enterprise Ireland, Medtronic Vascular, Galway
ID Code:14917
Deposited On:12 Nov 2009 13:34 by Caitriona Lally. Last Modified 12 Nov 2009 13:34

Download statistics

Archive Staff Only: edit this record