Schmidt S P, Monajjem N, Evancho M M, Pippert T R, Sharp W V
Vascular Research Laboratory, Akron City Hospital, OH 44309.
J Invest Surg. 1988;1(1):35-44. doi: 10.3109/08941938809141074.
One obstacle to the clinical implementation of endothelial cell seeding of vascular prostheses is the difficulty in derivation of large numbers of autologous endothelial cells from blood vessels of patients requiring vascular grafting. Capillary endothelial cells obtained from fat have been suggested as an abundant alternative to large-vessel endothelium for graft seeding. The object of this study was to evaluate the performance of 4-mm internal diameter (ID) Dacron Microvel grafts seeded with omentally derived microvascular endothelial cells. Six-cm lengths of the test grafts were implanted bilaterally into canine carotid arteries. One of each pair of grafts was seeded with endothelial cells (means = 8.4 x 10(6)) derived from collagenase digestion of autologous omental fat samples. The contralateral graft of each pair was nonseeded. At 5 weeks postoperatively, the grafts were harvested and evaluated. The mean patencies of both the seeded and nonseeded grafts were 89 percent. The mean thrombus-free surface area for seeded grafts was 95 +/- 11 percent. This value was significantly different statistically from the mean thrombus-free surface area of nonseeded grafts, which was 43 +/- 19 percent (P less than .05). Histologically, midgraft regions of seeded grafts were cellular, stained positive for collagen, and were characterized by inner capsules ranging in thickness between 35-94 microns. Luminal cells were identified as endothelial by peroxidase antiperoxidase staining techniques. Midgraft regions of nonseeded grafts demonstrated thrombus accumulation, limited cellularity, and inner capsules between 59-194 microns thick. Scanning electron microscopy of seeded grafts revealed smooth luminal surfaces with tight junctions between adjacent cells; surface cells were not present on midgraft regions of nonseeded grafts. In conclusion, endothelial cells derived from omental fat successfully surfaced on Dacron grafts and imparted characteristics to the graft that would predict long-term graft success.
血管假体进行内皮细胞种植的临床应用面临一个障碍,即从需要血管移植的患者血管中获取大量自体内皮细胞存在困难。已有人提出,从脂肪中获取的毛细血管内皮细胞可作为丰富的替代来源,用于替代大血管内皮细胞进行移植物种植。本研究的目的是评估种植了来自网膜的微血管内皮细胞的内径4毫米的涤纶微孔血管移植物的性能。将6厘米长的测试移植物双侧植入犬颈动脉。每对移植物中的一个种植来自自体网膜脂肪样本胶原酶消化得到的内皮细胞(均值 = 8.4×10⁶)。每对移植物的对侧移植物不进行种植。术后5周,取出移植物并进行评估。种植和未种植移植物的平均通畅率均为89%。种植移植物的平均无血栓表面积为95±11%。该值与未种植移植物的平均无血栓表面积(43±19%)在统计学上有显著差异(P<0.05)。组织学上,种植移植物的移植物中部区域有细胞,胶原染色呈阳性,其特征是内膜厚度在35 - 94微米之间。通过过氧化物酶抗过氧化物酶染色技术将腔内细胞鉴定为内皮细胞。未种植移植物的移植物中部区域显示有血栓积聚、细胞数量有限,内膜厚度在59 - 194微米之间。种植移植物的扫描电子显微镜检查显示管腔表面光滑,相邻细胞间有紧密连接;未种植移植物的移植物中部区域没有表面细胞。总之,来自网膜脂肪的内皮细胞成功地在涤纶移植物表面生长,并赋予移植物一些可预测长期移植物成功的特征。