The mechanobiology of articular cartilage development and degeneration

被引:247
作者
Carter, DR [1 ]
Beaupré, GS [1 ]
Wong, M [1 ]
Smith, RL [1 ]
Andriacchi, TP [1 ]
Schurman, DJ [1 ]
机构
[1] Vet Affairs Hlth Care Syst, Rehabil Res & Dev Ctr 153, Palo Alto, CA USA
关键词
D O I
10.1097/01.blo.0000144970.05107.7e
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The development, maintenance, and destruction of cartilage are regulated by mechanical factors throughout life. Mechanical cues in the cartilage fetal endoskeleton influence the expression of genes that guide the processes of growth, vascular invasion, and ossification. Intermittent fluid pressure maintains the cartilage phenotype whereas mild tension (or shear) promotes growth and ossification. The articular cartilage thickness is determined by the position at which the subchondral growth front stabilizes. In mature joints, cartilage is thickest and healthiest where the contact pressure and cartilage fluid pressure are greatest. The depth-dependent histomorphology reflects the local fluid pressure, tensile strain, and fluid exudation. Osteoarthritis represents the final demise and loss of cartilage in the skeletal elements. The initiation and progression of osteoarthritis can follow many pathways and can be promoted by mechanical factors including: (1) reduced loading, which activates the subchondral growth front by reducing fluid pressure; (2) blunt impact, causing microdamage and activation of the subchondral growth front by local shear stress; (3) mechanical abnormalities that increase wear at the articulating surface; and (4) other mechanically related factors. Research should be directed at integrating our mechanical understanding of osteoarthritis pathogenesis and progression within the framework of cellular and molecular events throughout ontogeny.
引用
收藏
页码:S69 / S77
页数:9
相关论文
共 54 条
[1]   A framework for the in vivo pathomechanics of osteoarthritis at the knee [J].
Andriacchi, TP ;
Mündermann, A ;
Smith, RL ;
Alexander, EJ ;
Dyrby, CO ;
Koo, S .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (03) :447-457
[2]  
Beaupré GS, 2000, J REHABIL RES DEV, V37, P145
[3]   The influence of strenuous exercise on collagen characteristics of articular cartilage in Thoroughbreds age 2 years [J].
Brama, PAJ ;
Tekoppele, JM ;
Bank, RA ;
Barneveld, A ;
Firth, EC ;
van Weeren, PR .
EQUINE VETERINARY JOURNAL, 2000, 32 (06) :551-554
[4]  
Bullough P, 1973, J Bone Joint Surg Br, V55, P746
[5]  
Bullough P., 1992, Osteoarthritis, P39
[6]  
BULLOUGH P G, 1976, Bulletin of the Hospital for Joint Diseases, V37, P110
[7]   Microfractures and microcracks in subchondral bone: are they relevant to osteoarthrosis? [J].
Burr, DB ;
Radin, EL .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2003, 29 (04) :675-+
[8]   Ruthenium hexaammine trichloride chemography for aggrecan mapping in cartilage is a sensitive indicator of matrix degradation [J].
Buschmann, MD ;
Maurer, AM ;
Berger, E ;
Perumbuli, P ;
Hunziker, EB .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (01) :81-88
[9]  
Carter D. R., 2001, SKELETAL FUNCTION FO
[10]   Modelling cartilage mechanobiology [J].
Carter, DR ;
Wong, M .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 2003, 358 (1437) :1461-1471