Goldring Mary B, Tsuchimochi Kaneyuki, Ijiri Kosei
Department of Medicine, Division of Rheumatology, Beth Israel Deaconess Medical Center, New England Baptist Bone and Joint Institute and Harvard Medical School, Boston, MA 02115, USA.
J Cell Biochem. 2006 Jan 1;97(1):33-44. doi: 10.1002/jcb.20652.
Chondrogenesis is the earliest phase of skeletal development, involving mesenchymal cell recruitment and migration, condensation of progenitors, and chondrocyte differentiation, and maturation and resulting in the formation of cartilage and bone during endochondral ossification. This process is controlled exquisitely by cellular interactions with the surrounding matrix, growth and differentiation factors, and other environmental factors that initiate or suppress cellular signaling pathways and transcription of specific genes in a temporal-spatial manner. Vertebrate limb development is controlled by interacting patterning systems involving prominently the fibroblast growth factor (FGF), bone morphogenetic protein (BMP), and hedgehog pathways. Both positive and negative signaling kinases and transcription factors, such as Sox9 and Runx2, and interactions among them determine whether the differentiated chondrocytes remain within cartilage elements in articular joints or undergo hypertrophic maturation prior to ossification. The latter process requires extracellular matrix remodeling and vascularization controlled by mechanisms that are not understood completely. Recent work has revealed novel roles for mediators such as GADD45beta, transcription factors of the Dlx, bHLH, leucine zipper, and AP-1 families, and the Wnt/beta-catenin pathway that interact at different stages during chondrogenesis.
软骨形成是骨骼发育的最早阶段,涉及间充质细胞的募集与迁移、祖细胞的凝聚、软骨细胞的分化、成熟,并在软骨内成骨过程中导致软骨和骨的形成。这一过程通过细胞与周围基质、生长和分化因子以及其他环境因子的相互作用而受到精确调控,这些因子以时空方式启动或抑制细胞信号通路以及特定基因的转录。脊椎动物肢体发育受相互作用的模式系统控制,其中显著涉及成纤维细胞生长因子(FGF)、骨形态发生蛋白(BMP)和刺猬信号通路。正向和负向信号激酶及转录因子,如Sox9和Runx2,以及它们之间的相互作用决定了分化的软骨细胞是留在关节软骨成分中,还是在骨化之前经历肥大成熟。后一过程需要细胞外基质重塑和血管生成,其控制机制尚未完全明了。最近的研究揭示了诸如GADD45β、Dlx、bHLH、亮氨酸拉链和AP-1家族转录因子以及Wnt/β-连环蛋白信号通路等介质在软骨形成不同阶段相互作用中的新作用。