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Sequential adaptation of perfusion and transport conditions significantly improves vascular construct recellularization and biomechanics

机译:灌注和运输条件的顺序适应显着改善了血管构建透气性和生物力学

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Abstract Recellularization of ex vivo‐derived scaffolds remains a significant hurdle primarily due to the scaffolds subcellular pore size that restricts initial cell seeding to the scaffolds periphery and inhibits migration over time. With the aim to improve cell migration, repopulation, and graft mechanics, the effects of a four‐step culture approach were assessed. Using an ex vivo‐derived vein as a model scaffold, human smooth muscle cells were first seeded onto its ablumen (Step 1: 3 hr) and an aggressive 0–100% nutrient gradient (lumenal flow under hypotensive pressure) was created to initiate cell migration across the scaffold (Step 2: Day 0 to 19). The effects of a prolonged aggressive nutrient gradient created by this single lumenal flow was then compared with a dual flow (lumenal and ablumenal) in Step 3 (Day 20 to 30). Analyses showed that a single lumenal flow maintained for 30 days resulted in a higher proportion of cells migrating across the scaffold toward the vessel lumen (nutrient source), with improved distribution. In Step 4 (Day 31 to 45), the transition from hypotensive pressure (12/8 mmHg) to normotensive (arterial‐like) pressure (120/80 mmHg) was assessed. It demonstrated that recellularized scaffolds exposed to arterial pressures have increased glycosaminoglycan deposition, physiological modulus, and Young's modulus. By using this stepwise conditioning, the challenging recellularization of a vein‐based scaffold and its positive remodeling toward arterial biomechanics were obtained.
机译:摘要出现前体内衍生的支架的缩进仍然是由于支架亚细胞孔径,其限制初始细胞周围的初始细胞周围并抑制随时间迁移的冠状动动型亚细胞孔径。旨在改善细胞迁移,重新迁移和移植力学,评估四步培养方法的影响。使用例如exvivo衍生的静脉作为模型支架,首先将人的光滑肌细胞接种到其Ablumen上(步骤1:3小时),并产生腐蚀性的0-100%营养梯度(在降压压力下的腔流量)以引发细胞在脚手架上迁移(步骤2:第0天至19)。然后将通过该单个腔流动产生的长期侵蚀性营养梯度的效果与步骤3(第20至30天)的双流量(LumeNal和Ablumal)进行比较。分析表明,保持30天的单个腔流量,导致较高比例的细胞,朝向血管腔(营养源)迁移到血管内,具有改进的分布。在步骤4(第31至45天)中,评估从降压压力(12/8mmHg)至正常(动脉样)压力(120/80mmHg)的转变。它证明了暴露于动脉压力的细胞间化支架增加了糖胺聚糖沉积,生理模量和杨氏模量增加。通过使用该逐步调节,获得了静脉制的支架的挑战速度和其朝向动脉生物力学的阳性重塑。

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