Kitoh Hiroshi, Ishiguro Naoki
Nagoya University School of Medicine, Department of Orthopaedic Surgery.
Clin Calcium. 2007 Apr;17(4):493-8.
The differentiation of chondocytes is well regulated by the interactions of a variety of growth factors, cytokines, and signal molecules. Bone morphogenetic proteins (BMPs) and Sry-box 9 (SOX9) , which play important roles in the process of mesenchymal condensations, promote chondrocyte differentiation and proliferation. Parathyroid hormone related peptide (PTHrP) and Indian hedgehog (Ihh) modulate the rate of cartilage differentiation through the formation of a negative feedback loop. Fibroblast growth factor receptor 3 (FGFR3) inhibits chondrocytes proliferation and enhances their differentiation into the hypertrophic phenotype. Here, we summarize the functions of these molecules and their networks for the differentiation and maturation of chondrocytes.
软骨细胞的分化受到多种生长因子、细胞因子和信号分子相互作用的良好调控。骨形态发生蛋白(BMPs)和性别决定区Y盒9(SOX9)在间充质凝聚过程中发挥重要作用,促进软骨细胞的分化和增殖。甲状旁腺激素相关肽(PTHrP)和印度刺猬因子(Ihh)通过形成负反馈环来调节软骨分化的速率。成纤维细胞生长因子受体3(FGFR3)抑制软骨细胞增殖,并增强其向肥大表型的分化。在此,我们总结这些分子的功能及其在软骨细胞分化和成熟过程中的网络关系。