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Biomimetic Nucleus Pulposus Scaffold Created from Bovine Caudal Intervertebral Disc Tissue Utilizing an Optimal Decellularization Procedure

机译:从牛尾椎间盘组织利用最佳脱细胞程序创建仿生髓核支架。

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摘要

Intervertebral disc (IVD) degeneration (IDD) and herniation (IDH) can result in low back pain and impart significant socioeconomic burden. These pathologies involve detrimental alteration to the nucleus pulposus (NP) either via biochemical degradation or extrusion from the IVD, respectively. Thus, engineering living NP tissue utilizing biomaterial scaffolds that recapitulate native NP microarchitecture, biochemistry, mechanical properties and which support cell viability represents an approach to aiding patients with IDD and IDH. To date, an ideal biomaterial to support NP regeneration has yet to be developed; however, one promising approach to generating biomimetic materials is to employ the decellularization (decell) of xenogeneic NP tissue to remove host DNA while maintaining critical native extracellular matrix (ECM) components. Herein, 13 different procedures were evaluated in an attempt to decell bovine caudal IVD NP tissue. An optimal method was identified which was confirmed to effectively remove bovine DNA, while maintaining physiologically relevant amounts of glycosaminoglycan (GAG) and type-II collagen. Unconfined static and dynamic compressive mechanical properties of scaffolds approached values reported for human NP and viability of human amniotic stem cells (hAMSCs) was maintained on non-crosslinked and EDC/NHS treated scaffolds for up to 14 days in culture. Taken together, NP tissue obtained from bovine caudal IVDs can be successfully decelled in order to generate a biomimetic scaffold for NP tissue regeneration.
机译:椎间盘(IVD)变性(IDD)和椎间盘突出(IDH)可能导致腰痛,并给社会经济带来沉重负担。这些病理涉及分别通过生化降解或从IVD挤出对髓核(NP)的有害改变。因此,利用生物材料支架工程化活的NP组织,该支架概括了天然NP的微体系结构,生物化学,机械特性并支持细胞活力,这是一种帮助IDD和IDH患者的方法。迄今为止,尚未开发出支持NP再生的理想生物材料。但是,一种产生仿生材料的有前途的方法是利用异种NP组织的脱细胞作用(decell)去除宿主DNA,同时保持关键的天然细胞外基质(ECM)成分。在本文中,评估了13种不同的程序,以尝试去除牛尾IVD NP组织。确定了一种最佳方法,该方法被证实可以有效去除牛DNA,同时保持生理相关量的糖胺聚糖(GAG)和II型胶原蛋白。支架的无侧限静态和动态压缩机械性能接近人类NP报道的值,并且人类羊膜干细胞(hAMSC)的活力在未交联且经EDC / NHS处理的支架上保持培养14天。综上所述,从牛尾部IVD获得的NP组织可以成功脱细胞,以生成用于NP组织再生的仿生支架。

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