Blum Jana C, Schenck Thilo L, Birt Alexandra, Giunta Riccardo E, Wiggenhauser Paul S
Department of Hand Surgery, Plastic Surgery and Aesthetic Surgery, Ludwig Maximilian University of Munich, Munich, Germany.
Department of Breast Surgery, Plastic Surgery and Aesthetic Surgery, Frauenklinik Dr. Geisenhofer GmbH, München, Germany.
J Tissue Eng. 2021 Jun 28;12:20417314211022242. doi: 10.1177/20417314211022242. eCollection 2021 Jan-Dec.
Ideal tissue engineering frameworks should be both an optimal biological microenvironment and a shape and stability providing framework. In this study we tried to combine the advantages of cell-derived artificial extracellular matrix (ECM) with those of 3D printed polycaprolactone (PCL) scaffolds. In Part A, both chondrogenic and osteogenic ECMs were produced by human adipose derived stem cells (hASCs) on 3D-printed PCL scaffolds and then decellularized to create cell free functionalized PCL scaffolds, named acPCL and aoPCL respectively. The decellularization resulted in a significant reduction of the DNA content as well as the removal of nuclei while the ECM was largely preserved. In Part B the bioactivation and the effect of the ac/aoPCL scaffolds on the proliferation, differentiation, and gene expression of hASCs was investigated. The ac/aoPCL scaffolds were found to be non-toxic and allow good adhesion, but do not affect proliferation. In the in vitro investigation of cartilage regeneration, biochemical analysis showed that acPCL scaffolds have an additional effect on chondrogenic differentiation as gene expression analysis showed markers of cartilage hypertrophy. The aoPCL showed a large influence on the differentiation of hASCs. In control medium they were able to stimulate hASCs to produce calcium alone and all genes relevant investigated for osteogenesis were significantly higher expressed on aoPCL than on unmodified PCL. Therefore, we believe that ac/aoPCL scaffolds have a high potential to improve regenerative capacity of unmodified PCL scaffolds and should be further investigated.
理想的组织工程支架应既是一个最佳的生物微环境,又是一个能提供形状和稳定性的支架。在本研究中,我们试图将细胞衍生的人工细胞外基质(ECM)的优势与3D打印聚己内酯(PCL)支架的优势相结合。在A部分,通过人脂肪来源干细胞(hASC)在3D打印的PCL支架上产生软骨生成和骨生成ECM,然后进行脱细胞处理以创建无细胞功能化PCL支架,分别命名为acPCL和aoPCL。脱细胞处理导致DNA含量显著降低以及细胞核的去除,而ECM在很大程度上得以保留。在B部分,研究了ac/aoPCL支架对hASC增殖、分化和基因表达的生物激活作用及影响。发现ac/aoPCL支架无毒且具有良好的黏附性,但不影响增殖。在软骨再生的体外研究中,生化分析表明acPCL支架对软骨生成分化有额外作用,因为基因表达分析显示了软骨肥大的标志物。aoPCL对hASC的分化有很大影响。在对照培养基中,它们能够单独刺激hASC产生钙,并且在aoPCL上所有与成骨相关的研究基因的表达均显著高于未修饰的PCL。因此,我们认为ac/aoPCL支架具有提高未修饰PCL支架再生能力的巨大潜力,应进一步研究。