J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, 1275 Center Drive, Biomedical Sciences Building, JG-56, Gainesville, FL 32611, USA.
Biotechnol Bioeng. 2013 Jul;110(7):2035-45. doi: 10.1002/bit.24934. Epub 2013 Apr 29.
The regeneration of functional, clinically viable, tissues from acellular ex vivo tissues has been problematic largely due to poor nutrient transport conditions that limit cell migration and integration. Compounding these issues are subcellular pore sizes that necessarily requires extracellular matrix (ECM) remodeling in order for cells to migrate and regenerate the tissue. The aim of the present work was to create a directed growth environment that allows cells to fully populate an ex vivo-derived vascular scaffold and maintain viability over extended periods. Three different culture conditions using single (one nutrient source) or dual perfusion bioreactor systems (two nutrients sources) were designed to assess the effect of pressure and nutrient gradients under either low (50/30 mmHg) or high (120/80) relative pressure conditions. Human myofibroblasts were seeded to the ablumenal periphery of an ex vivo-derived vascular scaffold using a collagen/hydrogel cell delivery system. After 30 days culture, total cell density was consistent between groups; however, significant variation was noted in cell distribution and construct mechanics as a result of differing perfusion conditions. The most aggressive transport gradient was developed by the single perfusion low-pressure circuits and resulted in a higher proportion of cells migrating across the scaffold toward the vessel lumen (nutrient source). These investigations illustrate the influence of directed nutrient gradients where precisely controlled perfusion conditions significantly affects cell migration, distribution and function, resulting in pronounced effects on construct mechanics during early remodeling events.
由于细胞迁移和整合的营养物质传输条件较差,使得从无细胞的离体组织中再生具有功能的、临床上可行的组织一直存在问题。使问题更加复杂的是亚细胞孔径大小,为了让细胞迁移并再生组织,必然需要细胞外基质(ECM)重塑。本研究的目的是创建一个定向生长环境,使细胞能够完全填充离体衍生的血管支架,并在延长的时间内保持活力。设计了三种不同的培养条件,使用单(一种营养源)或双(两种营养源)灌注生物反应器系统,以评估在相对低压(50/30mmHg)或高压(120/80mmHg)条件下压力和营养梯度的影响。使用胶原/水凝胶细胞输送系统将人肌成纤维细胞接种到离体衍生的血管支架的内腔周围。培养 30 天后,各组的总细胞密度保持一致;然而,由于灌注条件的不同,细胞分布和构建力学存在显著差异。单灌注低压回路形成的最具侵略性的传输梯度导致更多的细胞向血管腔(营养源)迁移穿过支架。这些研究说明了定向营养梯度的影响,其中精确控制的灌注条件显著影响细胞迁移、分布和功能,从而在早期重塑事件中对构建力学产生显著影响。