Integrins and chondrocyte-matrix interactions in articular cartilage

被引:214
作者
Loeser, Richard F. [1 ]
机构
[1] Univ N Carolina, Sch Med, Div Rheumatol Allergy & Immunol, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
Integrin; Cartilage; Chondrocyte; Osteoarthritis; Cell signaling; FIBRONECTIN FRAGMENTS; CELL-ADHESION; ALPHA-5-BETA-1; INTEGRIN; SIGNAL-TRANSDUCTION; GENE-EXPRESSION; PROTEIN; ACTIVATION; BINDING; KINASE; OSTEOARTHRITIS;
D O I
10.1016/j.matbio.2014.08.007
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
The integrin family of cell adhesion receptors plays a major role in mediating interactions between cells and the extracellular matrix. Normal adult articular chondrocytes express alpha 1 beta 1, alpha 3 beta 1, alpha 5 beta 1, alpha 10 beta 1, alpha V beta 1, alpha V beta 3, and alpha V beta 5 integrins, while chondrocytes from osteoarthritic tissue also express alpha 2 beta 1, alpha 4 beta 1, alpha 6 beta 1. These integrins bind a host of cartilage extracellular matrix (ECM) proteins, most notably fibronectin and collagen types II and VI, which provide signals that regulate cell proliferation, survival, differentiation, and matrix remodeling. By initiating signals in response to mechanical forces, chondrocyte integrins also serve as mechanotransducers. When the cartilage matrix is damaged in osteoarthritis, fragments of fibronectin are generated that signal through the alpha 5 beta 1 integrin to activate a pro-inflammatory and pro-catabolic response which, if left unchecked, could contribute to progressive matrix degradation. The cell signaling pathways activated in response to excessive mechanical signals and to fibronectin fragments are being unraveled and may represent useful therapeutic targets for slowing or stopping progressive matrix destruction in arthritis. (C) 2014 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
引用
收藏
页码:11 / 16
页数:6
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