Department of Mechanical and Aerospace Engineering, The George Washington University, Washington DC 20052, United States of America.
Nanotechnology. 2018 May 4;29(18):185101. doi: 10.1088/1361-6528/aaafa1. Epub 2018 Feb 15.
Cartilage tissue is prone to degradation and has little capacity for self-healing due to its avascularity. Tissue engineering, which provides artificial scaffolds to repair injured tissues, is a novel and promising strategy for cartilage repair. 3D bioprinting offers even greater potential for repairing degenerative tissue by simultaneously integrating living cells, biomaterials, and biological cues to provide a customized scaffold. With regard to cell selection, mesenchymal stem cells (MSCs) hold great capacity for differentiating into a variety of cell types, including chondrocytes, and could therefore be utilized as a cartilage cell source in 3D bioprinting. In the present study, we utilize a tabletop stereolithography-based 3D bioprinter for a novel cell-laden cartilage tissue construct fabrication. Printable resin is composed of 10% gelatin methacrylate (GelMA) base, various concentrations of polyethylene glycol diacrylate (PEGDA), biocompatible photoinitiator, and transforming growth factor beta 1 (TGF-β1) embedded nanospheres fabricated via a core-shell electrospraying technique. We find that the addition of PEGDA into GelMA hydrogel greatly improves the printing resolution. Compressive testing shows that modulus of the bioprinted scaffolds proportionally increases with the concentrations of PEGDA, while swelling ratio decreases with the increase of PEGDA concentration. Confocal microscopy images illustrate that the cells and nanospheres are evenly distributed throughout the entire bioprinted construct. Cells grown on 5%/10% (PEGDA/GelMA) hydrogel present the highest cell viability and proliferation rate. The TGF-β1 embedded in nanospheres can keep a sustained release up to 21 d and improve chondrogenic differentiation of encapsulated MSCs. The cell-laden bioprinted cartilage constructs with TGF-β1-containing nanospheres is a promising strategy for cartilage regeneration.
软骨组织由于其无血管性,容易降解,自我修复能力有限。组织工程为修复受损组织提供了人工支架,是一种新颖且有前途的软骨修复策略。3D 生物打印通过同时整合活细胞、生物材料和生物信号,提供定制化的支架,为修复退行性组织提供了更大的潜力。就细胞选择而言,间充质干细胞(MSCs)具有分化为多种细胞类型的巨大潜力,包括软骨细胞,因此可作为 3D 生物打印中的软骨细胞来源。在本研究中,我们利用基于桌面立体光刻的 3D 生物打印机制造新型细胞负载软骨组织构建体。可打印树脂由 10%的明胶甲基丙烯酰基(GelMA)基质、不同浓度的聚乙二醇二丙烯酸酯(PEGDA)、生物相容性光引发剂和通过核壳电喷雾技术制造的 TGF-β1 嵌入式纳米球组成。我们发现,PEGDA 加入 GelMA 水凝胶中可极大地提高打印分辨率。压缩测试表明,生物打印支架的模量与 PEGDA 的浓度成正比增加,而溶胀比随 PEGDA 浓度的增加而降低。共焦显微镜图像表明,细胞和纳米球均匀分布在整个生物打印构建体中。在 5%/10%(PEGDA/GelMA)水凝胶上生长的细胞表现出最高的细胞活力和增殖率。纳米球中嵌入的 TGF-β1 可以持续释放长达 21 天,并促进包封的 MSCs 的软骨分化。含有 TGF-β1 的纳米球的细胞负载生物打印软骨构建体是软骨再生的有前途的策略。