Document Type
Dissertation
Degree
Doctor of Philosophy (PhD)
Major/Program
Biomedical Engineering
First Advisor's Name
Sharan Ramaswamy
First Advisor's Committee Title
Committee Chair
Second Advisor's Name
Lidia Kos
Second Advisor's Committee Title
Committee Member
Third Advisor's Name
Wei-Chiang Lin
Third Advisor's Committee Title
Committee Member
Fourth Advisor's Name
Nikolaos Tsoukias
Fourth Advisor's Committee Title
Committee Member
Fifth Advisor's Name
Vinu Unnikrishnan
Fifth Advisor's Committee Title
Committee Member
Keywords
Tissue Engineering, Stem Cell, Heart Valve
Date of Defense
3-20-2015
Abstract
Heart valve disease occurs in adults as well as in pediatric population due to age-related changes, rheumatic fever, infection or congenital condition. Current treatment options are limited to mechanical heart valve (MHV) or bio-prosthetic heart valve (BHV) replacements. Lifelong anti-coagulant medication in case of MHV and calcification, durability in case of BHV are major setbacks for both treatments. Lack of somatic growth of these implants require multiple surgical interventions in case of pediatric patients. Advent of stem cell research and regenerative therapy propose an alternative and potential tissue engineered heart valves (TEHV) treatment approach to treat this life threatening condition. TEHV has the potential to promote tissue growth by replacing and regenerating a functional native valve. Hemodynamics play a crucial role in heart valve tissue formation and sustained performance. The focus of this study was to understand the role of physiological shear stress and flexure effects on de novo HV tissue formation as well as resulting gene and protein expression. A bioreactor system was used to generate physiological shear stress and cyclic flexure. Human bone marrow mesenchymal stem cell derived tissue constructs were exposed to native valve-like physiological condition. Responses of these tissue constructs to the valve-relevant stress states along with gene and protein expression were investigated after 22 days of tissue culture. We conclude that the combination of steady flow and cyclic flexure helps support engineered tissue formation by the co-existence of both OSS and appreciable shear stress magnitudes, and potentially augment valvular gene and protein expression when both parameters are in the physiological range.
Identifier
FI15050204
Recommended Citation
Rath, Sasmita, "Regulation of Bone Marrow Stem Cells through Oscillatory Shear Stresses - A Heart Valve Tissue Engineering Perspective" (2015). FIU Electronic Theses and Dissertations. 1824.
https://digitalcommons.fiu.edu/etd/1824
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