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Development of a whole organ culture model for intervertebral disc disease.用于椎间盘疾病的全器官培养模型的开发。
J Orthop Translat. 2015 Aug 29;5:1-8. doi: 10.1016/j.jot.2015.08.002. eCollection 2016 Apr.
2
Annular puncture with tumor necrosis factor-alpha injection enhances painful behavior with disc degeneration in vivo.环形穿刺联合注射肿瘤坏死因子-α会增强体内椎间盘退变时的疼痛行为。
Spine J. 2016 Mar;16(3):420-31. doi: 10.1016/j.spinee.2015.11.019. Epub 2015 Dec 2.
3
A Novel Organ Culture Model of Mouse Intervertebral Disc Tissues.一种新型的小鼠椎间盘组织器官培养模型。
Cells Tissues Organs. 2016;201(1):38-50. doi: 10.1159/000439268. Epub 2015 Oct 9.
4
The high-throughput phenotyping of the viscoelastic behavior of whole mouse intervertebral discs using a novel method of dynamic mechanical testing.使用一种新型动态力学测试方法对整个小鼠椎间盘的粘弹性行为进行高通量表型分析。
J Biomech. 2015 Jul 16;48(10):2189-94. doi: 10.1016/j.jbiomech.2015.04.040. Epub 2015 May 6.
5
Organ culture bioreactors--platforms to study human intervertebral disc degeneration and regenerative therapy.器官培养生物反应器——用于研究人类椎间盘退变与再生治疗的平台。
Curr Stem Cell Res Ther. 2015;10(4):339-52. doi: 10.2174/1574888x10666150312102948.
6
Genetic and functional studies of the intervertebral disc: a novel murine intervertebral disc model.椎间盘的遗传与功能研究:一种新型小鼠椎间盘模型。
PLoS One. 2014 Dec 4;9(12):e112454. doi: 10.1371/journal.pone.0112454. eCollection 2014.
7
The global burden of low back pain: estimates from the Global Burden of Disease 2010 study.全球腰痛负担:来自 2010 年全球疾病负担研究的估计。
Ann Rheum Dis. 2014 Jun;73(6):968-74. doi: 10.1136/annrheumdis-2013-204428. Epub 2014 Mar 24.
8
Novel imaging of the intervertebral disk and pain.椎间盘与疼痛的新影像学研究
Global Spine J. 2013 Jun;3(3):127-32. doi: 10.1055/s-0033-1347930. Epub 2013 May 30.
9
Role of cytokines in intervertebral disc degeneration: pain and disc content.细胞因子在椎间盘退变中的作用:疼痛和椎间盘内容物。
Nat Rev Rheumatol. 2014 Jan;10(1):44-56. doi: 10.1038/nrrheum.2013.160. Epub 2013 Oct 29.
10
Organ culture stability of the intervertebral disc: rat versus rabbit.椎间盘器官培养稳定性:大鼠与兔。
J Orthop Res. 2013 Jun;31(6):838-46. doi: 10.1002/jor.22285. Epub 2013 Mar 1.

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.

DOI:10.1002/jor.23325
PMID:27273204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5324835/
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。