Department of Plastic and Reconstructive Surgery, Shanghai 9th People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.
Biomaterials. 2011 Mar;32(9):2265-73. doi: 10.1016/j.biomaterials.2010.11.078. Epub 2010 Dec 30.
Acellular cartilage can provide a native extracellular matrix for cartilage engineering. However, it is difficult for cells to migrate into acellular cartilage because of its non-porous structure. The aim of this study is to establish a sandwich model for engineering cartilage with acellular cartilage sheets and chondrocytes. Cartilage from adult pig ear was cut into a circular cylinder with a diameter of approximately 6 mm and freeze-sectioned at thicknesses of 10 μm and 30 μm. The sheets were then decellularized and lyophilized. Chondrocytes isolated from newborn pig ear were expanded for 2 passages. The acellular sheets and chondrocytes were then stacked layer-by-layer, in a sandwich model, and cultured in dishes. After 4 weeks of cultivation, the constructs were then either maintained in culture for another 12 weeks or implanted subcutaneously in nude mouse. Histological analysis showed that cells were completely removed from cartilage sheets after decellularization. By re-seeding cells and stacking 20 layers of sheets together, a cylinder-shaped cell sheet was achieved. Cartilage-like tissues formed after 4 weeks of culture. Histological analyses showed the formation of cartilage with a typical lacunar structure. Cartilage formation was more efficient with 10 μm-thick sheets than with 30 μm sheets. Mature cartilage was achieved after 12 weeks of implantation, which was demonstrated by histology and confirmed by Safranin O, Toluidine blue and anti-type II collagen antibody staining. Furthermore, we achieved cartilage with a designed shape by pre-shaping the sheets prior to implantation. These results indicate that the sandwich model could be a useful model for engineering cartilage in vitro and in vivo.
去细胞软骨可为软骨工程提供天然的细胞外基质。然而,由于其非多孔结构,细胞很难迁移到去细胞软骨中。本研究旨在建立一种使用去细胞软骨片和软骨细胞工程软骨的三明治模型。从成年猪耳中切取直径约 6mm 的圆形圆柱体,然后将其冷冻切成 10μm 和 30μm 的厚度。然后将这些薄片去细胞化并冻干。从新生猪耳中分离的软骨细胞经过 2 代扩增。然后将去细胞片和软骨细胞层层叠放在三明治模型中,并在培养皿中培养。培养 4 周后,将构建体在培养中再维持 12 周,或皮下植入裸鼠。组织学分析表明,去细胞化后软骨片中的细胞被完全去除。通过重新接种细胞并将 20 层薄片堆叠在一起,实现了圆柱形细胞片。培养 4 周后形成了类似软骨的组织。组织学分析表明形成了具有典型腔隙结构的软骨。与 30μm 厚的薄片相比,使用 10μm 厚的薄片形成软骨的效率更高。植入 12 周后获得成熟的软骨,这通过组织学证实,并通过番红 O、甲苯胺蓝和抗 II 型胶原抗体染色得到确认。此外,我们通过在植入前对薄片进行预成型,实现了具有设计形状的软骨。这些结果表明,三明治模型可以成为体外和体内工程软骨的有用模型。