Fasol R, Zilla P, Deutsch M, Fischlein T, Kadletz M, Griesmacher A, Müller M M
Department of Surgery 2, University of Vienna, Vienna, Austria.
Tex Heart Inst J. 1987 Jun;14(2):119-26.
To evaluate the possibility of providing, in vitro, an endothelial lining for artificial hearts, we cultivated adult autologous endothelial cells on two polyurethane and two silicone rubber surfaces. Over the ensuing 11-day period, we investigated the resulting cell proliferation and morphology by means of scanning electron and light microscopy. On the silicone rubber surfaces, seeding of 200,000 human saphenous vein endothelial cells per cm(2) produced an ideal cobblestone monolayer within a single day. In contrast, the polyurethane surfaces displayed an uneven, patchy distribution of endothelial cells. Scanning electron microscopy revealed microvilli and marginal overlapping in both groups. After the first day, the cell count on the polyurethane surfaces increased, whereas the count on the silicone rubber surfaces decreased. Morphologic investigations revealed that the ideally shaped cells initially on the silicone rubber had begun to overspread and subsequently to become detached, leaving denuded spheroid areas. Moreover, cultivation for 11 days on the polyurethane surfaces resulted in an unevenness of cell distribution that far exceeded the unevenness seen on the first day. Thus, despite the fact that materials with a high surface tension (such as silicone rubbers) seem to be ideal for initial cell spreading, subsequent cultivation results in cell detachment and death. On materials with a lower surface tension (such as polyurethanes), the less differentiated monolayers do at least proliferate, although their morphology remains unsatisfactory. Even if adult human endothelial cells should prove shear-stress-resistant, a minimum of 6 to 8 weeks would be required to establish autologous endothelial cell monolayers on the inner surface. Therefore, the endothelialization of artificial hearts is not possible when such hearts are used for urgent "bridging" before cardiac transplantation.
为了评估在体外为人工心脏提供内皮衬里的可能性,我们在两种聚氨酯和两种硅橡胶表面培养了成年自体内皮细胞。在随后的11天里,我们通过扫描电子显微镜和光学显微镜研究了细胞的增殖情况和形态。在硅橡胶表面,每平方厘米接种200,000个人大隐静脉内皮细胞,一天内就能形成理想的鹅卵石状单层细胞。相比之下,聚氨酯表面的内皮细胞分布不均匀且呈斑块状。扫描电子显微镜显示两组细胞均有微绒毛和边缘重叠现象。第一天后,聚氨酯表面的细胞数量增加,而硅橡胶表面的细胞数量减少。形态学研究表明,最初在硅橡胶表面形状理想的细胞开始过度生长,随后脱落,留下裸露的球状区域。此外,在聚氨酯表面培养11天后,细胞分布的不均匀程度远远超过第一天观察到的情况。因此,尽管表面张力高的材料(如硅橡胶)似乎非常适合细胞的初始铺展,但后续培养会导致细胞脱落和死亡。在表面张力较低的材料(如聚氨酯)上,虽然单层细胞的分化程度较低,但至少会增殖,尽管其形态仍不尽人意。即使成年人类内皮细胞被证明具有抗剪切应力的能力,在内表面建立自体内皮细胞单层至少也需要6至8周时间。因此,当人工心脏用于心脏移植前的紧急“搭桥”时,实现其内皮化是不可能的。