Walter B A, Illien-Jünger S, Nasser P R, Hecht A C, Iatridis J C
Leni & Peter W. May Department of Orthopaedics, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Department of Biomedical Engineering, The City College of New York, New York, NY, USA.
Leni & Peter W. May Department of Orthopaedics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J Biomech. 2014 Jun 27;47(9):2095-101. doi: 10.1016/j.jbiomech.2014.03.015. Epub 2014 Mar 27.
Intervertebral disc (IVD) degeneration is a common cause of back pain, and attempts to develop therapies are frustrated by lack of model systems that mimic the human condition. Human IVD organ culture models can address this gap, yet current models are limited since vertebral endplates are removed to maintain cell viability, physiological loading is not applied, and mechanical behaviors are not measured. This study aimed to (i) establish a method for isolating human IVDs from autopsy with intact vertebral endplates, and (ii) develop and validate an organ culture loading system for human or bovine IVDs. Human IVDs with intact endplates were isolated from cadavers within 48h of death and cultured for up to 21 days. IVDs remained viable with ~80% cell viability in nucleus and annulus regions. A dynamic loading system was designed and built with the capacity to culture 9 bovine or 6 human IVDs simultaneously while applying simulated physiologic loads (maximum force: 4kN) and measuring IVD mechanical behaviors. The loading system accurately applied dynamic loading regimes (RMS error <2.5N and total harmonic distortion <2.45%), and precisely evaluated mechanical behavior of rubber and bovine IVDs. Bovine IVDs maintained their mechanical behavior and retained >85% viable cells throughout the 3 week culture period. This organ culture loading system can closely mimic physiological conditions and be used to investigate response of living human and bovine IVDs to mechanical and chemical challenges and to screen therapeutic repair techniques.
椎间盘(IVD)退变是背痛的常见原因,然而由于缺乏能够模拟人类情况的模型系统,开发相关治疗方法的尝试屡屡受挫。人类IVD器官培养模型可以填补这一空白,但目前的模型存在局限性,因为为了维持细胞活力需要去除椎体终板,未施加生理负荷,也未测量力学行为。本研究旨在:(i)建立一种从尸检中分离带有完整椎体终板的人类IVD的方法,以及(ii)开发并验证一种用于人类或牛IVD的器官培养加载系统。在死亡后48小时内从尸体中分离出带有完整终板的人类IVD,并培养长达21天。IVD在髓核和纤维环区域保持存活,细胞活力约为80%。设计并构建了一种动态加载系统,该系统能够同时培养9个牛IVD或6个人类IVD,同时施加模拟生理负荷(最大力:4kN)并测量IVD的力学行为。该加载系统能够准确施加动态加载模式(均方根误差<2.5N,总谐波失真<2.45%),并精确评估橡胶和牛IVD的力学行为。在整个3周的培养期内,牛IVD保持其力学行为,并且保留了超过85%的活细胞。这种器官培养加载系统可以紧密模拟生理条件,用于研究活体人类和牛IVD对机械和化学刺激的反应,以及筛选治疗修复技术。