Ingram Joanne Helen, Korossis Sotirios, Howling Graeme, Fisher John, Ingham Eileen
Faculties of Engineering and Biological Sciences, Institute of Medical and Biological Engineering, University of Leeds, Leeds, West Yorkshire, United Kingdom.
Tissue Eng. 2007 Jul;13(7):1561-72. doi: 10.1089/ten.2006.0362.
Tissue engineering offers a promising solution to the replacement of anterior cruciate ligament. A decellularized porcine patella tendon scaffold was produced by immersing whole tissues sequentially in hypotonic buffer, 0.1% (w/v) sodium dodecyl sulfate (SDS) in hypotonic buffer, and nuclease solution prior to sterilization with 0.1% (w/v) peracetic acid. Initial studies revealed that primary human tenocytes would attach to, but failed to penetrate into, the decellularized scaffold. A novel use of ultrasonication was therefore developed to allow extrinsic cells to migrate into the acellular scaffold. Various intensities of ultrasonication were tested in order to produce a microscopically more open porous matrix without damaging the overall architecture of the scaffold. Ultrasonication treatment with the intensity of 360 W and a pulse time of 1 s for a total of 1 min was found to be the optimal treatment. This process did not have a significant effect upon the biochemical constituents (collagen, glycosaminoglycans), nor did it denature the collagen. Moreover, the acellular sonicated scaffold retained the essential biomechanical characteristics of the native tissue. Primary human tenocytes penetrated into the center of whole acellular sonicated scaffolds over a 3-week period in static culture. The viability of the cells in the center of the scaffold (depth of circa 2.5 mm) was, however, compromised. To circumvent the problem of nutrient limitation, acellular sonicated scaffolds were split into fascicular scaffolds (500 mum thick). Cells seeded onto the fascicular scaffolds penetrated throughout the scaffold and remained viable after 3 weeks of culture. This study has shown that an acellular biocompatible tendon scaffold can be produced using 0.1% (w/v) SDS and that ultrasonication can provide a novel method to enhance the recellularization of decellularized natural tissues.
组织工程为前交叉韧带的替代提供了一个有前景的解决方案。通过将整个组织依次浸入低渗缓冲液、含0.1%(w/v)十二烷基硫酸钠(SDS)的低渗缓冲液和核酸酶溶液中,然后用0.1%(w/v)过氧乙酸进行灭菌,制备了去细胞猪髌腱支架。初步研究表明,原代人肌腱细胞能够附着在去细胞支架上,但无法穿透。因此,开发了一种超声处理的新方法,以使外源性细胞迁移到无细胞支架中。测试了不同强度的超声处理,以产生在显微镜下更开放的多孔基质,同时不破坏支架的整体结构。发现强度为360 W、脉冲时间为1 s、总时长为1 min的超声处理是最佳处理方法。该过程对生化成分(胶原蛋白、糖胺聚糖)没有显著影响,也没有使胶原蛋白变性。此外,无细胞超声处理的支架保留了天然组织的基本生物力学特性。在静态培养的3周时间内,原代人肌腱细胞穿透了整个无细胞超声处理支架的中心。然而,支架中心(深度约2.5 mm)的细胞活力受到了影响。为了规避营养限制问题,将无细胞超声处理的支架分割成束状支架(500μm厚)。接种到束状支架上的细胞在整个支架中均有穿透,并且在培养3周后仍保持活力。这项研究表明,使用0.1%(w/v)SDS可以制备无细胞生物相容性肌腱支架,并且超声处理可以提供一种新方法来增强去细胞天然组织的再细胞化。