Eybl E, Grimm M, Grabenwöger M, Böck P, Müller M M, Wolner E
Second Department of Surgery, University of Vienna, Austria.
J Thorac Cardiovasc Surg. 1992 Sep;104(3):763-9.
To investigate the conditions for endothelial cell lining of glutaraldehyde-treated bioprosthetic heart valves, we examined in vitro the growth properties of endothelial cells on clinically used pericardial valve material and on glutaraldehyde-fixed pericardium treated with L-glutamic acid. To improve endothelial cell attachment to the valvular surface, we precoated both materials either with fibronectin or with fibrillar collagen (95% type I, 5% type III). Toxicity of glutaraldehyde, released from clinically used valve material, caused endothelial cell death, independent of the type of precoating. Treatment of the valve material with L-glutamic acid resulted in regular endothelial cell proliferation. We found that collagenous precoating, compared with fibronectin precoating, markedly enhanced endothelial cell proliferation and attachment (p less than 0.05). Maintenance of antithrombogenic potency of the seeded cells on L-glutamic acid-treated valve material was proved by regular release of prostacyclin. We conclude that bioprosthetic heart valve materials can be lined with endothelial cells if toxic glutaraldehyde released from the bioprostheses is eliminated.
为了研究经戊二醛处理的生物人工心脏瓣膜内皮细胞衬里的条件,我们在体外检测了内皮细胞在临床使用的心包瓣膜材料以及用L - 谷氨酸处理的戊二醛固定心包上的生长特性。为了改善内皮细胞与瓣膜表面的附着,我们用纤连蛋白或纤维状胶原蛋白(95% I型,5% III型)预涂这两种材料。临床使用的瓣膜材料释放的戊二醛毒性导致内皮细胞死亡,与预涂层类型无关。用L - 谷氨酸处理瓣膜材料可导致内皮细胞正常增殖。我们发现,与纤连蛋白预涂层相比,胶原蛋白预涂层显著增强了内皮细胞的增殖和附着(p小于0.05)。通过前列环素的正常释放证明了接种在L - 谷氨酸处理的瓣膜材料上的细胞具有抗血栓形成能力。我们得出结论,如果消除生物假体释放的有毒戊二醛,生物人工心脏瓣膜材料可以内衬内皮细胞。