1 Institute of Biomaterials and Biomedical Engineering, University of Toronto , Toronto, Canada .
2 BioEngineering of Skeletal Tissues Team, Pathology and Laboratory Medicine, Mount Sinai Hospital, Lunenfeld Tanenbaum Research Institute, University of Toronto , Toronto, Canada .
Tissue Eng Part A. 2017 Sep;23(17-18):1001-1010. doi: 10.1089/ten.TEA.2016.0433. Epub 2017 Jul 11.
The intervertebral disc (IVD) is composed of nucleus pulposus (NP) surrounded by multilamellated annulus fibrosus (AF), and is located between the vertebral bodies. Current treatments for chronic neck or low back pain do not completely restore the functionality of degenerated IVDs. Thus, developing biological disc replacements is an approach of great interest. Given the complex structure of the IVD, tissue engineering of the individual IVD components and then combining them together may be the only way to achieve this. The engineered disc must then be able to integrate into the host spine to ensure mechanical stability. The goal of this study was to generate an integrated model of an IVD in vitro. Multilamellated AF tissues were generated in vitro using aligned nanofibrous polycarbonate urethane scaffolds and AF cells. After 3 weeks in culture, it was placed around NP tissue formed on and integrated with a porous bone substitute material (calcium polyphosphate). The two tissues were cocultured to fabricate the IVD model. The AF tissue composed of six lamellae containing type I collagen-rich extracellular matrix (ECM) and the NP tissue had type II collagen- and aggrecan-rich ECM. Immunofluorescence studies showed both type I and II collagen at the AF-NP interface. There was evidence of integration of the tissues. The peel test for AF lamellae showed an interlamellar shear stress of 0.03 N/mm. The AF and NP were integrated as the pushout test demonstrated that the AF-NP interface had significantly increased mechanical stability by 2 weeks of coculture. To evaluate if these tissues remained integrated, allogeneic IVD model constructs were implanted into defects freshly made in the NP-inner AF and bone of the bovine coccygeal spine. One month postimplantation, the interfaces between the AF lamellae remained intact and there was integration with the host AF tissue. No inflammatory reaction was noted at this time period. In summary, an engineered IVD implant with mechanically stable integration between AF lamellae and AF-NP can be generated in vitro. Further study is required to scale up the size of this construct and evaluate its ability to serve as a biological disc replacement.
椎间盘(IVD)由被多层纤维环(AF)包围的髓核(NP)组成,位于椎体之间。目前治疗慢性颈部或腰部疼痛的方法并不能完全恢复退化的 IVD 的功能。因此,开发生物椎间盘替代品是一种非常有意义的方法。鉴于 IVD 的复杂结构,对单个 IVD 成分进行组织工程化,然后将它们组合在一起可能是实现这一目标的唯一方法。工程化的椎间盘必须能够与宿主脊柱整合,以确保机械稳定性。本研究的目的是在体外生成一个完整的 IVD 模型。使用排列的纳米纤维聚碳酸酯聚氨酯支架和 AF 细胞在体外生成多层纤维环组织。培养 3 周后,将其放置在多孔骨替代材料(磷酸钙)上形成并整合的 NP 组织周围。两种组织被共培养以制造 IVD 模型。由富含 I 型胶原蛋白的细胞外基质(ECM)组成的 6 层 AF 组织和富含 II 型胶原蛋白和聚集蛋白聚糖的 NP 组织。免疫荧光研究显示在 AF-NP 界面处存在 I 型和 II 型胶原蛋白。有组织整合的证据。AF 层压板的剥离试验显示层间剪切应力为 0.03 N/mm。随着共培养 2 周的推进试验表明,AF-NP 界面的机械稳定性显著增加,AF 和 NP 得到了整合。为了评估这些组织是否仍然保持整合,同种异体 IVD 模型构建体被植入牛尾骨脊柱 NP-内纤维环和骨的新鲜缺损中。植入后 1 个月,AF 层压板之间的界面保持完整,并与宿主纤维环组织整合。此时没有观察到炎症反应。总之,可以在体外生成具有 AF 层压板和 AF-NP 之间机械稳定整合的工程化 IVD 植入物。需要进一步研究来扩大这种构建体的尺寸,并评估其作为生物椎间盘替代品的能力。