Involvement of the cytoskeletal elements in articular cartilage homeostasis and pathology

被引:86
作者
Blain, Emma J. [1 ]
机构
[1] Cardiff Univ, Sch Biosci, Connect Tissue Biol Labs, Cardiff CF10 3US, S Glam, Wales
关键词
actin microfilaments; articular cartilage; chondrocyte; cytoskeleton; tubulin microtubules; vimentin intermediate filaments; HYDROSTATIC-PRESSURE; GENE-EXPRESSION; CELL-SHAPE; IN-VITRO; INTERMEDIATE-FILAMENTS; HUMAN CHONDROCYTES; ACTIN-FILAMENTS; CYTOCHALASIN-D; PROTEOGLYCAN SYNTHESIS; VIMENTIN CYTOSKELETON;
D O I
10.1111/j.1365-2613.2008.00625.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The cytoskeleton of all cells is a three-dimensional network comprising actin microfilaments, tubulin microtubules and intermediate filaments. Studies in many cell types have indicated roles for these cytoskeletal proteins in many diverse cellular processes including alteration of cell shape, movement of organelles, migration, endocytosis, secretion, cell division and extracellular matrix assembly. The cytoskeletal networks are highly organized in structure enabling them to fulfil their biological functions. This review will primarily focus on the organization and function of the three major cytoskeletal networks in articular cartilage chondrocytes. Articular cartilage is a major load-bearing tissue of the synovial joint; it is well known that the cytoskeleton acts as a physical interface between the chondrocytes and the extracellular matrix in 'sensing' mechanical stimuli. The effect of mechanical load on cytoskeletal element expression and organization will also be reviewed. Abnormal mechanical load is widely believed to be a risk factor for the development of osteoarthritis. Several studies have intimated that the major cytoskeletal networks are disorganized or often absent in osteoarthritic cartilage chondrocytes. The implications and possible reasoning for this are more widely discussed and placed into context with their potential relevance to disease and therapeutic strategies.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 116 条
[31]   The ARP2/3 complex: an actin nucleator comes of age [J].
Goley, Erin D. ;
Welch, Matthew D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (10) :713-726
[32]  
Gomez J, 1997, J IMMUNOL, V158, P1516
[33]   Cartilage tissue remodeling in response to mechanical forces [J].
Grodzinsky, AJ ;
Levenston, ME ;
Jin, M ;
Frank, EH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2000, 2 :691-+
[34]   CORRELATION BETWEEN TUMOR NECROSIS FACTOR-ALPHA(TNF-ALPHA)-INDUCED CYTOSKELETAL CHANGES AND HUMAN COLLAGENASE GENE INDUCTION [J].
GRONOWICZ, G ;
HADJIMICHAEL, J ;
RICHARDS, D ;
CERAMI, A ;
ROSSOMANDO, EF .
JOURNAL OF PERIODONTAL RESEARCH, 1992, 27 (06) :562-568
[35]   Compression-induced changes in the shape and volume of the chondrocyte nucleus [J].
Guilak, F .
JOURNAL OF BIOMECHANICS, 1995, 28 (12) :1529-+
[36]  
Hayes AJ, 1999, DEV DYNAM, V215, P179, DOI 10.1002/(SICI)1097-0177(199907)215:3<179::AID-AJA1>3.3.CO
[37]  
2-H
[38]   CELL LOCOMOTION - NEW RESEARCH TESTS OLD IDEAS ON MEMBRANE AND CYTOSKELETAL FLOW [J].
HEATH, JP ;
HOLIFIELD, BF .
CELL MOTILITY AND THE CYTOSKELETON, 1991, 18 (04) :245-257
[39]   Alterations in the vimentin cytoskeleton in response to single impact load in an in vitro model of cartilage damage in the rat [J].
Henson, Frances M. D. ;
Vincent, Thea A. .
BMC MUSCULOSKELETAL DISORDERS, 2008, 9 (1)
[40]   Intermediate filaments and their associates: multi-talented structural elements specifying cytoarchitecture and cytodynamics [J].
Herrmann, H ;
Aebi, U .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (01) :79-90