Mechanisms of synovial joint and articular cartilage development

被引:81
作者
Chijimatsu, Ryota [1 ]
Saito, Taku [2 ]
机构
[1] Univ Tokyo, Grad Sch Med, Bone & Cartilage Regenerat Med, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138655, Japan
[2] Univ Tokyo, Grad Sch Med, Sensory & Motor Syst Med, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138655, Japan
基金
日本学术振兴会;
关键词
Articular cartilage; Joint; Interzone; Chondrocyte; BONE MORPHOGENETIC PROTEIN; FIBROBLAST GROWTH FACTOR-18; HORMONE-RELATED PEPTIDE; MEK-ERK PATHWAY; 4 HUMAN EMBRYOS; INDIAN HEDGEHOG; TGF-BETA; CHONDROCYTE PROLIFERATION; ENDOCHONDRAL BONE; MOUSE LIMB;
D O I
10.1007/s00018-019-03191-5
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
Articular cartilage is formed at the end of epiphyses in the synovial joint cavity and permanently contributes to the smooth movement of synovial joints. Most skeletal elements develop from transient cartilage by a biological process known as endochondral ossification. Accumulating evidence indicates that articular and growth plate cartilage are derived from different cell sources and that different molecules and signaling pathways regulate these two kinds of cartilage. As the first sign of joint development, the interzone emerges at the presumptive joint site within a pre-cartilage tissue. After that, joint cavitation occurs in the center of the interzone, and the cells in the interzone and its surroundings gradually form articular cartilage and the synovial joint. During joint development, the interzone cells continuously migrate out to the epiphyseal cartilage and the surrounding cells influx into the joint region. These complicated phenomena are regulated by various molecules and signaling pathways, including GDF5, Wnt, IHH, PTHrP, BMP, TGF-beta, and FGF. Here, we summarize current literature and discuss the molecular mechanisms underlying joint formation and articular development.
引用
收藏
页码:3939 / 3952
页数:14
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