Sirois E, Charara J, Ruel J, Dussault J C, Gagnon P, Doillon C J
Biomaterials Institute of Quebec, CHUQ, Quebec City, Canada.
Biomaterials. 1998 Nov;19(21):1925-34. doi: 10.1016/s0142-9612(98)00094-5.
After injury and vascular replacement, endothelial cell recovery is limited and could lead to thrombosis. Seeding small diameter vascular prosthesis with endothelial cells has been proposed to fulfil cell lining and improve surface hemocompatibility. However, detachment of seeded cells occurs following implantation. Previous in vitro studies have looked at the fluid shear stress as a major cause of cell detachment. To our knowledge, the role of erythrocyte collisions has not been investigated. The present in vitro study aims at investigating whether endothelial cell adhesion depends on (i) the presence of erythrocytes in flow and (ii) the latent culture period (1, 24 and 48 h) between seeding and exposure to flow. Endothelial cells were exposed to culture media containing different erythrocyte concentrations using a steady laminar flow of 1350 ml min(-1) in a parallel plate flow chamber. Endothelial cell morphology in dynamic conditions was quantified and compared to that in static conditions. The projected area of cells were mostly found smaller under dynamic than static conditions, particularly at a wall shear stress of 23 dyn cm(-2). Cells from the 1 h latent culture period were oriented parallel to the flow axis and were more elongated than under static conditions. Conversely, endothelial cell shape was slightly modified when either the latent period or the wall shear stress was increased. Disparate orientation was observed on confluent endothelial cells (24-48 h latent period) exposed to shear stress with or without erythrocytes. Increasing fluid viscous forces due to erythrocytes play a critical role on the behaviour of freshly seeded endothelial cells upon exposure to blood flow.
损伤和血管置换后,内皮细胞的恢复有限,可能导致血栓形成。有人提出在小口径血管假体中接种内皮细胞以形成细胞内衬并改善表面血液相容性。然而,植入后接种的细胞会发生脱落。以往的体外研究认为流体剪切应力是细胞脱落的主要原因。据我们所知,红细胞碰撞的作用尚未得到研究。本体外研究旨在调查内皮细胞的黏附是否取决于:(i)流动中红细胞的存在;(ii)接种与暴露于流动之间的潜伏培养期(1、24和48小时)。使用平行板流动腔室中1350 ml min(-1)的稳定层流,将内皮细胞暴露于含有不同红细胞浓度的培养基中。对动态条件下的内皮细胞形态进行量化,并与静态条件下的形态进行比较。在动态条件下,细胞的投影面积大多比静态条件下小,尤其是在壁面剪应力为23 dyn cm(-2)时。潜伏培养1小时的细胞与流动轴平行排列,比静态条件下更细长。相反,当潜伏时间或壁面剪应力增加时,内皮细胞的形状会略有改变。在暴露于有或无红细胞剪切应力的汇合内皮细胞(潜伏24 - 48小时)上观察到不同的取向。红细胞引起的流体粘性力增加对新接种的内皮细胞在暴露于血流时的行为起着关键作用。