Juran Cassandra M, Dolwick M Franklin, McFetridge Peter S
1 J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida , Gainesville, Florida.
Tissue Eng Part A. 2015 Feb;21(3-4):829-39. doi: 10.1089/ten.TEA.2014.0250. Epub 2015 Jan 9.
The temporomandibular joint (TMJ) disc is susceptible to numerous pathologies that may lead to structural degradation and jaw dysfunction. The limited treatment options and debilitating nature of severe temporomandibular disorders has been the primary driving force for the introduction and development of TMJ disc tissue engineering as an approach to alleviate this important clinical issue. This study aimed to evaluate the efficacy of laser micropatterning (LMP) ex vivo-derived TMJ disc scaffolds to enhance cellular integration, a major limitation to the development of whole tissue implant technology. LMP was incorporated into the decellularized extracellular matrix scaffold structure using a 40 W CO2 laser ablation system to drill an 8×16 pattern with a bore diameter of 120 μm through the scaffold thickness. Disc scaffolds were seeded with human neonatal-derived umbilical cord mesenchymal stem cells differentiated into chondrocytes at a density of 900 cells per mm(2) and then assessed on days 1, 7, 14, and 21 of culture. Results derived from histology, PicoGreen DNA quantification, and cellular metabolism assays indicate that the LMP scaffolds improve cellular remodeling compared to the unworked scaffold over the 21-day culture period. Mechanical analysis further supports the use of the LMP showing the compressive properties of the LMP constructs closely represent native disc mechanics. The addition of an artificial path of infiltration by LMP culminated in improved chondrocyte adhesion, dispersion, and migration after extended culture aiding in recapitulating the native TMJ disc characteristics.
颞下颌关节(TMJ)盘易患多种疾病,这些疾病可能导致结构退化和颌功能障碍。严重颞下颌关节紊乱的治疗选择有限且性质使人衰弱,这一直是引入和发展颞下颌关节盘组织工程作为缓解这一重要临床问题的方法的主要驱动力。本研究旨在评估激光微图案化(LMP)体外衍生的颞下颌关节盘支架增强细胞整合的功效,细胞整合是全组织植入技术发展的一个主要限制因素。使用40W二氧化碳激光烧蚀系统将LMP纳入脱细胞细胞外基质支架结构,以在支架厚度上钻出直径为120μm的8×16图案。将盘状支架接种以每平方毫米900个细胞的密度分化为软骨细胞的人新生儿来源的脐带间充质干细胞,然后在培养的第1、7、14和21天进行评估。组织学、PicoGreen DNA定量和细胞代谢分析的结果表明,在21天的培养期内,与未处理的支架相比,LMP支架改善了细胞重塑。力学分析进一步支持LMP的使用,显示LMP构建体的压缩特性与天然盘状力学特性密切相似。通过LMP添加人工渗透路径最终在延长培养后改善了软骨细胞的粘附、分散和迁移,有助于重现天然颞下颌关节盘的特征。