Papageorgiou Iraklis, Abberton Thomas, Fuller Martin, Tipper Joanne L, Fisher John, Ingham Eileen
IMBE (Institute of Medical & Biological Engineering), School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
IMBE, School of Mechanical Engineering, University of Leeds, Leeds LS2 9JT, UK.
Nanomaterials (Basel). 2014 Jun 16;4(2):485-504. doi: 10.3390/nano4020485.
Medical interventions for the treatment of spinal disc degeneration include total disc replacement and fusion devices. There are, however, concerns regarding the generation of wear particles by these devices, the majority of which are in the nanometre sized range with the potential to cause adverse biological effects in the surrounding tissues. The aims of this study were to develop an organ culture model of the porcine dura mater and to investigate the biological effects of CoCr nanoparticles in this model. A range of histological techniques were used to analyse the structure of the tissue in the organ culture. The biological effects of the CoCr wear particles and the subsequent structural changes were assessed using tissue viability assays, cytokine assays, histology, immunohistochemistry, and TEM imaging. The physiological structure of the dura mater remained unchanged during the seven days of culture. There was no significant loss of cell viability. After exposure of the organ culture to CoCr nanoparticles, there was significant loosening of the epithelial layer, as well as the underlying collagen matrix. TEM imaging confirmed these structural alterations. These structural alterations were attributed to the production of MMP-1, -3, -9, -13, and TIMP-1. ELISA analysis revealed that there was significant release of cytokines including IL-8, IL-6, TNF-α, ECP and also the matrix protein, tenascin-C. This study suggested that CoCr nanoparticles did not cause cytotoxicity in the dura mater but they caused significant alterations to its structural integrity that could lead to significant secondary effects due to nanoparticle penetration, such as inflammation to the local neural tissue.
治疗椎间盘退变的医学干预措施包括全椎间盘置换和融合装置。然而,人们担心这些装置会产生磨损颗粒,其中大多数颗粒尺寸在纳米范围内,有可能对周围组织产生不良生物学影响。本研究的目的是建立猪硬脑膜的器官培养模型,并研究该模型中钴铬纳米颗粒的生物学效应。使用了一系列组织学技术来分析器官培养中组织的结构。使用组织活力测定、细胞因子测定、组织学、免疫组织化学和透射电镜成像来评估钴铬磨损颗粒的生物学效应以及随后的结构变化。在培养的七天中,硬脑膜的生理结构保持不变。细胞活力没有明显丧失。将器官培养物暴露于钴铬纳米颗粒后,上皮层以及下面的胶原基质出现明显疏松。透射电镜成像证实了这些结构改变。这些结构改变归因于MMP-1、-3、-9、-13和TIMP-1的产生。酶联免疫吸附测定分析显示,包括IL-8、IL-6、TNF-α、嗜酸性粒细胞阳离子蛋白以及基质蛋白肌腱蛋白-C在内的细胞因子有显著释放。本研究表明,钴铬纳米颗粒不会在硬脑膜中引起细胞毒性,但会导致其结构完整性发生显著改变,由于纳米颗粒的渗透可能导致显著的继发效应,如局部神经组织炎症。