| Literature DB >> 25079013 |
Yong-Ung Lee1, Tai Yi2, Iyore James2, Shuhei Tara2, Alexander J Stuber2, Kejal V Shah2, Avione Y Lee2, Tadahisa Sugiura2, Narutoshi Hibino3, Toshiharu Shinoka2, Christopher K Breuer4.
Abstract
Tissue engineered heart valves, especially decellularized valves, are starting to gain momentum in clinical use of reconstructive surgery with mixed results. However, the cellular and molecular mechanisms of the neotissue development, valve thickening, and stenosis development are not researched extensively. To answer the above questions, we developed a murine heterotopic heart valve transplantation model. A heart valve was harvested from a valve donor mouse and transplanted to a heart donor mouse. The heart with a new valve was transplanted heterotopically to a recipient mouse. The transplanted heart showed its own heartbeat, independent of the recipient's heartbeat. The blood flow was quantified using a high frequency ultrasound system with a pulsed wave Doppler. The flow through the implanted pulmonary valve showed forward flow with minimal regurgitation and the peak flow was close to 100 mm/sec. This murine model of heart valve transplantation is highly versatile, so it can be modified and adapted to provide different hemodynamic environments and/or can be used with various transgenic mice to study neotissue development in a tissue engineered heart valve.Entities:
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Year: 2014 PMID: 25079013 PMCID: PMC4407638 DOI: 10.3791/51695
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355