Lee Yong-Ung, Yi Tai, James Iyore, Tara Shuhei, Stuber Alexander J, Shah Kejal V, Lee Avione Y, Sugiura Tadahisa, Hibino Narutoshi, Shinoka Toshiharu, Breuer Christopher K
Tissue Engineering Program and Surgical Research, Nationwide Children's Hospital;
Tissue Engineering Program and Surgical Research, Nationwide Children's Hospital.
J Vis Exp. 2014 Jul 23(89):51695. doi: 10.3791/51695.
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.
组织工程心脏瓣膜,尤其是去细胞化瓣膜,在重建手术的临床应用中开始获得发展势头,结果不一。然而,新组织发育、瓣膜增厚和狭窄发展的细胞和分子机制尚未得到广泛研究。为了回答上述问题,我们建立了一种小鼠异位心脏瓣膜移植模型。从瓣膜供体小鼠获取心脏瓣膜并移植到心脏供体小鼠。带有新瓣膜的心脏被异位移植到受体小鼠。移植的心脏显示出自身的心跳,独立于受体的心跳。使用带有脉冲波多普勒的高频超声系统对血流进行定量。通过植入肺动脉瓣的血流显示为前向血流,反流最小,峰值血流接近100毫米/秒。这种心脏瓣膜移植的小鼠模型具有高度的通用性,因此可以进行修改和调整以提供不同的血流动力学环境,和/或可与各种转基因小鼠一起使用,以研究组织工程心脏瓣膜中的新组织发育。