Erez E, Sandbank J, Stamler A, Raanani E, Sharoni E, Vidne B A, Barak J
Department of Cardiothoracic Surgery, Rabin Medical Center, Petah-Tikva, Israel.
J Heart Valve Dis. 2001 Jan;10(1):125-8.
In order to provide valved xenografts with reduced immunity, yet durability comparable with that of homografts, a method for endothelial cell removal was developed.
Adult porcine valved pulmonary conduits were isolated, washed and incubated in trypsin-EDTA solution. The endothelial cells were flushed free with a stream of culture medium, and the xenografts cryopreserved. Grafts were thawed after three months, and evaluated structurally.
Macroscopic inspection of the grafts revealed no cracks or other morphological damage. Light microscopy revealed mildly edematous changes, and the elastic layers appeared to be preserved. Incubation with trypsin-EDTA solution consistently removed the entire endothelial layer, without obvious damage to the underlying tissues.
With care and appropriate timing, the xenograft endothelium can be selectively removed, leaving the underlying tissue intact. This process may allow further structural manipulations to improve the durability of these grafts.
为了提供免疫性降低但耐久性与同种异体移植物相当的带瓣异种移植物,开发了一种去除内皮细胞的方法。
分离成年猪带瓣肺动脉导管,冲洗后在胰蛋白酶 - 乙二胺四乙酸(EDTA)溶液中孵育。用培养基流冲洗使内皮细胞游离,然后将异种移植物冷冻保存。三个月后将移植物解冻并进行结构评估。
对移植物的宏观检查未发现裂缝或其他形态损伤。光学显微镜检查显示有轻度水肿变化,弹性层似乎得以保留。用胰蛋白酶 - EDTA溶液孵育始终能去除整个内皮细胞层,而对其下方组织无明显损伤。
谨慎操作并把握适当时间,可以选择性地去除异种移植物的内皮,使下方组织保持完整。这一过程可能允许进行进一步的结构操作以提高这些移植物的耐久性。