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本文引用的文献

1
Differential response of human bone marrow stromal cells to either TGF-β(1) or rhGDF-5.人骨髓基质细胞对 TGF-β(1)或 rhGDF-5 的不同反应。
Eur Spine J. 2011 Jun;20(6):962-71. doi: 10.1007/s00586-010-1619-z. Epub 2010 Nov 18.
2
Influence of low glucose supply on the regulation of gene expression by nucleus pulposus cells and their responsiveness to mechanical loading.低葡萄糖供应对髓核细胞基因表达调控及其对机械加载响应的影响。
J Neurosurg Spine. 2010 Oct;13(4):535-42. doi: 10.3171/2010.4.SPINE09713.
3
The effect of running exercise on intervertebral disc extracellular matrix production in a rat model.跑步运动对大鼠模型椎间盘细胞外基质产生的影响。
Spine (Phila Pa 1976). 2010 Jul 1;35(15):1429-36. doi: 10.1097/BRS.0b013e3181e0f5bc.
4
Notochordal cell conditioned medium stimulates mesenchymal stem cell differentiation toward a young nucleus pulposus phenotype.脊索细胞条件培养基刺激间充质干细胞向年轻的髓核样表型分化。
Stem Cell Res Ther. 2010 Jun 16;1(2):18. doi: 10.1186/scrt18.
5
Low oxygen tension is a more potent promoter of chondrogenic differentiation than dynamic compression.低氧张力比动态压缩更能促进软骨细胞分化。
J Biomech. 2010 Sep 17;43(13):2516-23. doi: 10.1016/j.jbiomech.2010.05.020. Epub 2010 Jun 16.
6
The combined effects of limited nutrition and high-frequency loading on intervertebral discs with endplates.有限营养与高频加载对终板的椎间盘的联合作用。
Spine (Phila Pa 1976). 2010 Sep 1;35(19):1744-52. doi: 10.1097/BRS.0b013e3181c48019.
7
The role of mechanical signals in regulating chondrogenesis and osteogenesis of mesenchymal stem cells.机械信号在调节间充质干细胞软骨生成和成骨过程中的作用。
Birth Defects Res C Embryo Today. 2010 Mar;90(1):75-85. doi: 10.1002/bdrc.20173.
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Cryopreserved intervertebral disc with injected bone marrow-derived stromal cells: a feasibility study using organ culture.注射骨髓基质细胞的冷冻椎间盘:器官培养的可行性研究。
Spine J. 2010 Jun;10(6):486-96. doi: 10.1016/j.spinee.2009.12.019. Epub 2010 Feb 19.
9
Differential expression level of cytokeratin 8 in cells of the bovine nucleus pulposus complicates the search for specific intervertebral disc cell markers.细胞角蛋白 8 在牛髓核细胞中的差异表达水平使寻找特定椎间盘细胞标志物的研究变得复杂。
Arthritis Res Ther. 2010;12(1):R24. doi: 10.1186/ar2931. Epub 2010 Feb 12.
10
Transcriptional profiling of bovine intervertebral disc cells: implications for identification of normal and degenerate human intervertebral disc cell phenotypes.牛椎间盘细胞的转录组分析:对鉴定正常和退变人类椎间盘细胞表型的启示。
Arthritis Res Ther. 2010;12(1):R22. doi: 10.1186/ar2929. Epub 2010 Feb 11.

动态加载对椎间盘的影响。

The effects of dynamic loading on the intervertebral disc.

机构信息

ARTORG Center for Biomedical Engineering, Spine Research Center, Institute for Surgical Technology and Biomechanics, University of Bern, Stauffacherstrasse 78, 3014 Bern, Switzerland.

出版信息

Eur Spine J. 2011 Nov;20(11):1796-812. doi: 10.1007/s00586-011-1827-1. Epub 2011 May 4.

DOI:10.1007/s00586-011-1827-1
PMID:21541667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3207351/
Abstract

Loading is important to maintain the balance of matrix turnover in the intervertebral disc (IVD). Daily cyclic diurnal assists in the transport of large soluble factors across the IVD and its surrounding circulation and applies direct and indirect stimulus to disc cells. Acute mechanical injury and accumulated overloading, however, could induce disc degeneration. Recently, there is more information available on how cyclic loading, especially axial compression and hydrostatic pressure, affects IVD cell biology. This review summarises recent studies on the response of the IVD and stem cells to applied cyclic compression and hydrostatic pressure. These studies investigate the possible role of loading in the initiation and progression of disc degeneration as well as quantifying a physiological loading condition for the study of disc degeneration biological therapy. Subsequently, a possible physiological/beneficial loading range is proposed. This physiological/beneficial loading could provide insight into how to design loading regimes in specific system for the testing of various biological therapies such as cell therapy, chemical therapy or tissue engineering constructs to achieve a better final outcome. In addition, the parameter space of 'physiological' loading may also be an important factor for the differentiation of stem cells towards most ideally 'discogenic' cells for tissue engineering purpose.

摘要

负荷对于维持椎间盘(IVD)基质转换的平衡很重要。日常的周期性昼夜节律有助于大的可溶性因子在 IVD 及其周围循环中的运输,并对椎间盘细胞施加直接和间接的刺激。然而,急性机械损伤和累积性过载会导致椎间盘退变。最近,关于周期性负荷(尤其是轴向压缩和静水压力)如何影响 IVD 细胞生物学的信息越来越多。这篇综述总结了最近关于 IVD 和干细胞对施加的循环压缩和静水压力的反应的研究。这些研究探讨了负荷在椎间盘退变的起始和进展中的可能作用,并量化了椎间盘退变生物治疗研究的生理负荷条件。随后,提出了一个可能的生理/有益的负荷范围。这种生理/有益的负荷可以深入了解如何为各种生物治疗(如细胞治疗、化学治疗或组织工程构建体)设计特定系统中的负荷方案,以实现更好的最终结果。此外,“生理”负荷的参数空间对于干细胞向最理想的“椎间盘形成”细胞的分化也可能是一个重要因素,以实现组织工程的目的。