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小鼠器官培养模型中刺伤导致椎间盘结构和炎症反应的纵向变化

Longitudinal changes in the structure and inflammatory response of the intervertebral disc due to stab injury in a murine organ culture model.

作者信息

Abraham Adam C, Liu Jennifer W, Tang Simon Y

机构信息

Department of Orthopedic Surgery, Washington University in St. Louis, 660 S. Euclid, Campus Box 8233, St. Louis 63103, Missouri.

Department of Biomedical Engineering, Washington University in St. Louis, One Brookings Drive, Whitaker Hall, Campus Box 1097, St. Louis 63130, Missouri.

出版信息

J Orthop Res. 2016 Aug;34(8):1431-8. doi: 10.1002/jor.23325. Epub 2016 Aug 28.

Abstract

Despite the significant public health impact of intervertebral disc (IVD) degeneration and low back pain, it remains challenging to investigate the multifactorial molecular mechanisms that drive the degenerative cascade. Organ culture model systems offer the advantage of allowing cells to live and interact with their native extracellular matrix, while simultaneously reducing the amount of biological variation and complexity present at the organismal level. Murine organ cultures in particular also allow the use of widely available genetically modified animals with molecular level reporters that would reveal insights on the degenerative cascade. Here, we utilize an organ culture system of murine lumbar functional spinal units where we are able to maintain the cellular, metabolic, and structural, and mechanical stability of the whole organ over a 21-day period. Furthermore, we describe a novel approach in organ culture by using tissues from animals with an NF-κB-luc reporter in combination with a mechanical injury model, and are able to show that proinflammatory factors and cytokines such as NF-κB and IL-6 produced by IVD cells can be monitored longitudinally during culture in a stab injury model. Taken together, we utilize a murine organ culture system that maintains the cellular and tissue level behavior of the intervertebral disc and apply it to transgenic animals that allow the monitoring of the inflammatory profile of IVDs. This approach could provide important insights on the molecular and metabolic mediators that regulate the homeostasis of the IVD. © 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1431-1438, 2016.

摘要

尽管椎间盘(IVD)退变和腰痛对公众健康有重大影响,但研究驱动退变级联反应的多因素分子机制仍然具有挑战性。器官培养模型系统的优势在于能让细胞在其天然细胞外基质中存活并相互作用,同时减少生物体水平上存在的生物变异和复杂性。特别是小鼠器官培养还允许使用广泛可得的带有分子水平报告基因的基因改造动物,从而揭示退变级联反应的相关见解。在此,我们利用小鼠腰椎功能性脊柱单元的器官培养系统,在21天的时间内能够维持整个器官的细胞、代谢、结构和机械稳定性。此外,我们描述了一种器官培养的新方法,即使用来自带有NF-κB-荧光素酶报告基因动物的组织,并结合机械损伤模型,且能够表明在刺伤模型的培养过程中可纵向监测IVD细胞产生的促炎因子和细胞因子,如NF-κB和IL-6。综上所述,我们利用一种能维持椎间盘细胞和组织水平行为的小鼠器官培养系统,并将其应用于可监测IVD炎症特征的转基因动物。这种方法可为调节IVD稳态的分子和代谢介质提供重要见解。© 2016骨科研究协会。由威利期刊公司出版。《矫形外科学研究》34:1431 - 1438,2016年。

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