Chondrocyte apoptosis in development, aging and disease

被引:112
作者
Horton, WE [1 ]
Feng, LX [1 ]
Adams, C [1 ]
机构
[1] NIA, Gerontol Res Ctr, Biol Chem Lab, NIH, Baltimore, MD 21224 USA
关键词
D O I
10.1016/S0945-053X(98)90024-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is increasing evidence that chondrocyte apoptosis plays an important role in cartilage development, aging and disease. A variety of morphological and biochemical studies have identified apoptotic chondrocytes in both growth plate and articular cartilage of a variety of species. In addition, there is an ever increasing list of diverse stimuli that can induce chondrocyte apoptosis in vitro. A feedback loop regulating chondrocyte apoptosis in the growth plate has been described that includes Indian Hedgehog, parathyroid hormone-related protein and Bcl-2. The molecular mechanism regulating apoptosis in articular cartilage is still under investigation. Future studies should elucidate more fully how abnormal regulation of chondrocyte apoptosis may contribute to the development of chondrodysplasias and chondrosarcomas. Also, it will be of importance to define the relationship between chondrocyte apoptosis and the regulation of chondrocyte-specific gene expression.
引用
收藏
页码:107 / 115
页数:9
相关论文
共 53 条
[1]  
Adams CS, 1998, ANAT RECORD, V250, P418
[2]   Bcl-2 lies downstream of parathyroid hormone-related peptide in a signaling pathway that regulates chondrocyte maturation during skeletal development [J].
Amling, M ;
Neff, L ;
Tanaka, S ;
Inoue, D ;
Kuida, K ;
Weir, E ;
Philbrick, WM ;
Broadus, AE ;
Baron, R .
JOURNAL OF CELL BIOLOGY, 1997, 136 (01) :205-213
[3]  
ARENDS MJ, 1990, AM J PATHOL, V136, P593
[4]   HEDGEHOG AND BMP GENES ARE COEXPRESSED AT MANY DIVERSE SITES OF CELL-CELL INTERACTION IN THE MOUSE EMBRYO [J].
BITGOOD, MJ ;
MCMAHON, AP .
DEVELOPMENTAL BIOLOGY, 1995, 172 (01) :126-138
[5]  
BLANCO FJ, 1995, AM J PATHOL, V146, P75
[6]   Type II transglutaminase expression in rabbit articular chondrocytes in culture: Relation with cell differentiation, cell growth, cell adhesion and cell apoptosis [J].
Borge, L ;
Demignot, S ;
Adolphe, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1996, 1312 (02) :117-124
[7]  
Bronckers ALJJ, 1996, J BONE MINER RES, V11, P1281
[8]   Aging and cancer: The double-edged sword of replicative senescence [J].
Campisi, J .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1997, 45 (04) :482-488
[9]   Activation of the cell death program by inhibition of proteasome function [J].
Drexler, HCA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (03) :855-860
[10]  
EASTMAN A, 1995, METHOD CELL BIOL, V46, P41