Department of Materials Science and Engineering, Research Center for Biomolecular Nanotechnology, Gwangju Institute of Science and Technology, Gwangju 500-712, South Korea.
J Biomater Sci Polym Ed. 2010;21(8-9):1173-90. doi: 10.1163/092050609X12471222313524.
The tissue engineering of tendon was studied using highly elastic poly(L-lactide-co-epsilon-caprolactone) (PLCL) scaffolds and focusing on the effect of dynamic tensile stimulation. Tenocytes from rabbit Achilles tendon were seeded (1.0 x 10(6) cells/scaffold) onto porous PLCL scaffolds and cultured for periods of 2 weeks and 4 weeks. This was performed in a static system and also in a bioreactor equipped with tensile modulation which mimicked the environmental surroundings of tendons with respect to tensile extension. The degradation of the polymeric scaffolds during the culture was relatively slow. However, there was an indication that cells accelerated the degradation of PLCL scaffolds. The scaffold/cell adducts from the static culture exhibited inferior strength (at 2 weeks 350 kPa, 4 weeks 300 kPa) compared to the control without cells (at 2 weeks 460 kPa, 4 weeks 340 kPa), indicating that the cells contributed to the enhanced degradation. On the contrary, the corresponding values of the adducts from the dynamic culture (at 2 weeks 430 kPa, 4 weeks 370 kPa) were similar to, or higher than, those from the control. This could be explained by the increased quantity of cells and neo-tissues in the case of dynamic culture compensating for the loss in tensile strength. Compared with static and dynamic culture conditions, mechanical stimulation played a crucial role in the regeneration of tendon tissue. In the case of the dynamic culture system, cell proliferation was enhanced and secretion of collagen type I was increased, as evidenced by DNA assay and histological and immunofluorescence analysis. Thus, tendon regeneration, indicated by improved mechanical and biological properties, was demonstrated, confirming the effect of mechanical stimulation. It could be concluded that the dynamic tensile stimulation appeared to be an essential factor in tendon/ligament tissue engineering, and that elastic PLCL co-polymers could be very beneficial in this process.
采用高弹性聚(L-丙交酯-co-ε-己内酯)(PLCL)支架对肌腱组织工程进行了研究,并重点研究了动态拉伸刺激的效果。将兔跟腱的腱细胞(1.0×10(6)细胞/支架)接种到多孔 PLCL 支架上,并在静态系统和配备拉伸调制的生物反应器中培养 2 周和 4 周。拉伸调制模仿了肌腱的环境环境,以实现拉伸延伸。在培养过程中,聚合物支架的降解相对较慢。但是,有迹象表明细胞加速了 PLCL 支架的降解。与无细胞对照(2 周时 460 kPa,4 周时 340 kPa)相比,静态培养的支架/细胞结合物的强度较低(2 周时 350 kPa,4 周时 300 kPa),表明细胞有助于增强降解。相反,动态培养的结合物的相应值(2 周时 430 kPa,4 周时 370 kPa)与对照相似或更高。这可以通过在动态培养的情况下,细胞和新组织的数量增加来解释,这补偿了拉伸强度的损失。与静态和动态培养条件相比,机械刺激在肌腱组织再生中起着至关重要的作用。在动态培养系统中,细胞增殖增强,胶原 I 分泌增加,这可以通过 DNA 分析以及组织学和免疫荧光分析得到证明。因此,通过改善机械和生物学特性来证明了肌腱再生,证实了机械刺激的效果。可以得出结论,动态拉伸刺激似乎是肌腱/韧带组织工程的重要因素,而弹性 PLCL 共聚物在该过程中非常有益。