Programmed cell death in intervertebral disc degeneration

被引:336
作者
Zhao, Chang-Qing [1 ]
Jiang, Lei-Sheng [1 ]
Dai, Li-Yang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Orthoped Surg, Shanghai 200092, Peoples R China
关键词
intervertebral disc; degeneration; programmed cell death;
D O I
10.1007/s10495-006-0290-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Intervertebral disc (IVD) degeneration is largely a process of destruction and failure of the extracellular matrix (ECM), and symptomatic IVD degeneration is thought to be one of the leading causes of morbidity or life quality deterioration in the elderly. To date, however, the mechanism of IVD degeneration is still not fully understood. Cellular loss from cell death in the process of IVD degeneration has long been confirmed and considered to contribute to ECM degradation, but the causes and the manners of IVD cell death remain unclear. Programmed cell death (PCD) is executed by an active cellular process and is extensively involved in many physiological and pathological processes, including embryonic development and human degenerative diseases. Thus, the relationship between PCD and IVD degeneration has become a new research focus of interest in recent years. By reviewing the available literature concentrated on PCD in IVD and discussing the methodology of detecting PCD in IVD cells, its inducing factors, the relationship of cell death to ECM degradation, and the potential therapy for IVD degeneration by modulation of PCD, we conclude that IVD cells undergo PCD via different signal transduction pathways in response to different stimuli, that PCD may play a role in the process of IVD degeneration, and that modulation of PCD might be a potential therapeutic strategy for IVD degeneration.
引用
收藏
页码:2079 / 2088
页数:10
相关论文
共 95 条
[21]
Court C, 2001, Spine J, V1, P239, DOI 10.1016/S1529-9430(01)00056-0
[22]
Changes in collagen cross-linking in degenerative disc disease and scoliosis [J].
Duance, VC ;
Crean, JKG ;
Sims, TJ ;
Avery, N ;
Smith, S ;
Menage, J ;
Eisenstein, SM ;
Roberts, S .
SPINE, 1998, 23 (23) :2545-2551
[23]
AN IMPROVED METHOD FOR THE DETECTION OF DNA FRAGMENTATION [J].
FACCHINETTI, A ;
TESSAROLLO, L ;
MAZZOCCHI, M ;
KINGSTON, R ;
COLLAVO, D ;
BIASI, G .
JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 136 (01) :125-131
[24]
DISRUPTION OF EPITHELIAL CELL-MATRIX INTERACTIONS INDUCES APOPTOSIS [J].
FRISCH, SM ;
FRANCIS, H .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :619-626
[25]
Intervertebral disc tissue engineering II: Cultures of nucleus pulposus cells [J].
Gan, JC ;
Ducheyne, P ;
Vresilovic, EJ ;
Shapiro, IM .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2003, (411) :315-324
[26]
Disc chondrocyte transplantation in a canine model: A treatment for degenerated or damaged intervertebral disc [J].
Ganey, T ;
Libera, J ;
Moos, V ;
Alasevic, O ;
Fritsch, KG ;
Meisel, HJ ;
Hutton, WC .
SPINE, 2003, 28 (23) :2609-2620
[27]
IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[28]
GOLD R, 1994, LAB INVEST, V71, P219
[29]
Analysis of aging and degeneration of the human intervertebral disc - Comparison of surgical specimens with normal controls [J].
Gruber, HE ;
Hanley, EN .
SPINE, 1998, 23 (07) :751-757
[30]
Anti-apoptotic effects of IGF-1 and PDGF on human intervertebral disc cells in vitro [J].
Gruber, HE ;
Norton, HJ ;
Hanley, EN .
SPINE, 2000, 25 (17) :2153-2157