Transplantation of Pulmonary Valve Using a Mouse Model of Heterotopic Heart Transplantation

被引:5
|
作者
Lee, Yong-Ung [1 ,2 ]
Yi, Tai [1 ,2 ]
James, Iyore [1 ,2 ]
Tara, Shuhei [1 ,2 ]
Stuber, Alexander J. [1 ,2 ]
Shah, Kejal V. [1 ,2 ]
Lee, Avione Y. [1 ,2 ]
Sugiura, Tadahisa [1 ,2 ]
Hibino, Narutoshi [2 ]
Shinoka, Toshiharu [1 ,2 ]
Breuer, Christopher K. [1 ,2 ]
机构
[1] Nationwide Childrens Hosp, Tissue Engn Program, Columbus, OH 43205 USA
[2] Nationwide Childrens Hosp, Columbus, OH USA
来源
关键词
Medicine; Issue; 89; tissue engineering; pulmonary valve; congenital heart defect; decellularized heart valve; transgenic mouse model; heterotopic heart transplantation; LEAFLET REPLACEMENT; LAMB MODEL;
D O I
10.3791/51695
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:5
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