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本文引用的文献

1
Cartilage intermediate layer protein promotes lumbar disc degeneration.软骨中间层蛋白促进腰椎间盘退变。
Biochem Biophys Res Commun. 2014 Apr 18;446(4):876-81. doi: 10.1016/j.bbrc.2014.03.025. Epub 2014 Mar 14.
2
Bioactive factors in platelet-rich plasma obtained by apheresis.富含血小板血浆中的生物活性因子。
Transfus Med Hemother. 2013 Dec;40(6):432-40. doi: 10.1159/000356329. Epub 2013 Oct 27.
3
Dual release of dexamethasone and TGF-β3 from polymeric microspheres for stem cell matrix accumulation in a rat disc degeneration model.聚合物微球中地塞米松和 TGF-β3 的双重释放促进大鼠椎间盘退变模型中干细胞基质的积累。
Acta Biomater. 2013 Dec;9(12):9423-33. doi: 10.1016/j.actbio.2013.08.019. Epub 2013 Aug 22.
4
Development of poly(trimethylene carbonate) network implants for annulus fibrosus tissue engineering.用于纤维环组织工程的聚三亚甲基碳酸酯网络植入物的开发。
J Appl Biomater Funct Mater. 2012;10(3):177-84. doi: 10.5301/JABFM.2012.10354.
5
Exhaustion of nucleus pulposus progenitor cells with ageing and degeneration of the intervertebral disc.椎间盘老化和退变导致髓核祖细胞耗竭。
Nat Commun. 2012;3:1264. doi: 10.1038/ncomms2226.
6
Platelet-rich plasma effects on degenerative disc disease: analysis of histology and imaging in an animal model.富血小板血浆对椎间盘退变疾病的影响:动物模型的组织学与影像学分析
Evid Based Spine Care J. 2011 Nov;2(4):13-8. doi: 10.1055/s-0031-1274752.
7
Effect of autologous platelet-rich plasma-releasate on intervertebral disc degeneration in the rabbit anular puncture model: a preclinical study.自体富血小板血浆释放物对兔椎间盘穿刺模型椎间盘退变的影响:一项临床前研究。
Arthritis Res Ther. 2012 Nov 5;14(6):R241. doi: 10.1186/ar4084.
8
[An experimental study on effect of autologous platelet-rich plasma on treatment of early intervertebral disc degeneration].[自体富血小板血浆治疗早期椎间盘退变的效果实验研究]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2012 Aug;26(8):977-83.
9
Incidence and risk factors for lumbar degenerative disc disease in the United States military 1999-2008.1999 - 2008年美国军队中腰椎退行性椎间盘疾病的发病率及危险因素
Mil Med. 2011 Nov;176(11):1320-4. doi: 10.7205/milmed-d-11-00061.
10
Genetic susceptibility of intervertebral disc degeneration among young Finnish adults.年轻芬兰成年人椎间盘退变的遗传易感性。
BMC Med Genet. 2011 Nov 22;12:153. doi: 10.1186/1471-2350-12-153.

椎间盘退变的细胞与分子生物学:当前认识及对潜在治疗策略的启示

Cell and molecular biology of intervertebral disc degeneration: current understanding and implications for potential therapeutic strategies.

作者信息

Wang S Z, Rui Y F, Lu J, Wang C

机构信息

Department of Orthopaedics, Zhongda Hospital, Medical School of Southeast University, Nanjing, Jiangsu, 210009, China.

出版信息

Cell Prolif. 2014 Oct;47(5):381-90. doi: 10.1111/cpr.12121. Epub 2014 Aug 11.

DOI:10.1111/cpr.12121
PMID:25112472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6495969/
Abstract

Intervertebral disc degeneration (IDD) is a chronic, complex process associated with low back pain; mechanisms of its occurrence have not yet been fully elucidated. Its process is not only accompanied by morphological changes, but also by systematic changes in its histological and biochemical properties. Many cellular and molecular mechanisms have been reported to be related with IDD and to reverse degenerative trends, abnormal conditions of the living cells and altered cell phenotypes would need to be restored. Promising biological therapeutic strategies still rely on injection of active substances, gene therapy and cell transplantation. With advanced study of tissue engineering protocols based on cell therapy, combined use of seeding cells, bio-active substances and bio-compatible materials, are promising for IDD regeneration. Recently reported progenitor cells within discs themselves also hold prospects for future IDD studies. This article describes the background of IDD, current understanding and implications of potential therapeutic strategies.

摘要

椎间盘退变(IDD)是一种与腰痛相关的慢性复杂过程;其发生机制尚未完全阐明。该过程不仅伴随着形态学变化,还伴随着组织学和生化特性的系统性改变。据报道,许多细胞和分子机制与IDD相关,若要逆转退变趋势,需要恢复活细胞的异常状态并改变细胞表型。有前景的生物治疗策略仍依赖于活性物质注射、基因治疗和细胞移植。随着基于细胞治疗的组织工程方案的深入研究,种子细胞、生物活性物质和生物相容性材料的联合应用有望实现IDD再生。最近报道的椎间盘内的祖细胞也为未来的IDD研究带来了希望。本文介绍了IDD的背景、对潜在治疗策略的当前认识及意义。