Prendiville E J, Coleman J E, Callow A D, Gould K E, Laliberte-Verdon S, Ramberg K, Connolly R J
Department of Surgery, Tufts University School of Medicine, New England Medical Center Hospitals, Boston, Massachusetts.
Eur J Vasc Surg. 1991 Jun;5(3):311-9. doi: 10.1016/s0950-821x(05)80515-8.
Endothelial cell (EC) seeding is postulated as a mechanism of improving patency of small calibre vascular grafts. However, the majority of seeded cells are lost within hours following restoration of blood flow. We postulated that incubating EC in-vitro on a graft will improve adherence and resistance to the sheer stresses of pulsatile blood flow. Fibronectin-treated ePTFE (5 cm x 4 mm ID) seeded with Indium-111-labelled autologous canine EC (1.5 x 10(5) cells/cm2) were incubated for four different time periods; 90 min, 24 h, 72 h and 6 days. Incubated grafts were subjected to blood flow of 75 ml/min for 6 h, in a canine ex-vivo arteriovenous shunt circuit. EC retention during perfusion was studied by measuring gamma activity emitted by the grafts. Cell morphology of non-perfused control groups and perfused groups was compared using scanning electron microscopy (SEM). SEM of control grafts showed progressive EC spreading on the ePTFE surface for up to 72 h incubation. Gamma activity was significantly higher at 6 h perfusion in grafts incubated for 72 h (82 +/- 4%) and 24 h (63 +/- 6%) vs. 90 min (34 +/- 13%, p less than 0.05), and between grafts incubated for 72 h vs. 6 days (55 +/- 7%, p less than 0.05). Perfused grafts incubated for 72 h showed unaltered EC morphology on SEM, few cells remained on 90 min incubated grafts. We conclude that incubating EC on fibronectin-treated ePTFE for 72 h in-vitro after seeding improves cell retention during blood flow.
内皮细胞(EC)接种被认为是改善小口径血管移植物通畅性的一种机制。然而,大多数接种的细胞在恢复血流后的数小时内就会丢失。我们推测,在体外将内皮细胞接种在移植物上会提高其对搏动性血流切应力的黏附性和抵抗力。用纤连蛋白处理过的聚四氟乙烯(ePTFE,内径4mm,长5cm)接种铟-111标记的自体犬内皮细胞(1.5×10⁵个细胞/cm²),并在四个不同时间段进行孵育:90分钟、24小时、72小时和6天。将孵育后的移植物在犬体外动静脉分流回路中以75ml/min的血流灌注6小时。通过测量移植物发出的γ活性来研究灌注过程中内皮细胞的保留情况。使用扫描电子显微镜(SEM)比较未灌注对照组和灌注组的细胞形态。对照组移植物的扫描电子显微镜显示,在长达72小时的孵育过程中,内皮细胞在ePTFE表面逐渐铺展。在灌注6小时时,孵育72小时(82±4%)和24小时(63±6%)的移植物的γ活性显著高于孵育90分钟的移植物(34±13%,p<0.05),并且孵育72小时的移植物与孵育6天的移植物之间也存在显著差异(55±7%,p<0.05)。孵育72小时的灌注移植物在扫描电子显微镜下显示内皮细胞形态未改变,而孵育90分钟的移植物上几乎没有细胞残留。我们得出结论,接种后在体外将内皮细胞在纤连蛋白处理过的ePTFE上孵育72小时可提高血流过程中细胞的保留率。