Chen Xuesong, Macica Carolyn M, Nasiri Ali, Broadus Arthur E
Yale University School of Medicine, New Haven, Connecticut 06520-8020, USA.
Arthritis Rheum. 2008 Dec;58(12):3788-97. doi: 10.1002/art.23985.
Chondrocytes of the epiphyseal growth zone are regulated by the Indian hedgehog (IHH)-parathyroid hormone-related protein (PTHrP) axis. In weight-bearing joints, this growth zone comes to be subdivided by the secondary ossification center into distinct articular and growth cartilage structures. The purpose of this study was to explore the cells of origin, localization, regulation of expression, and putative functions of IHH and PTHrP in articular cartilage in the mouse.
We assessed IHH and PTHrP expression in an allelic PTHrP-LacZ-knockin mouse and several versions of PTHrP-null mice. Selected joints were unloaded surgically to examine load-induction of PTHrP and IHH.
The embryonic growth zone appears to serve as the source of PTHrP-expressing proliferative chondrocytes that populate both the forming articular cartilage and growth plate structures. In articular cartilage, these cells take the form of articular chondrocytes in the midzone. In PTHrP-knockout mice, mineralizing chondrocytes encroach upon developing articular cartilage but appear to be prevented from mineralizing the joint space by IHH-driven surface chondrocyte proliferation. In growing and adult mice, PTHrP expression in articular chondrocytes is load-induced, and unloading is associated with rapid changes in PTHrP expression and articular chondrocyte differentiation.
We conclude that the IHH-PTHrP axis participates in the maintenance of articular cartilage. Dysregulation of this system might contribute to the pathogenesis of arthritis.
骨骺生长区的软骨细胞受印度刺猬因子(IHH)-甲状旁腺激素相关蛋白(PTHrP)轴调控。在负重关节中,该生长区会被次级骨化中心细分为不同的关节软骨和生长软骨结构。本研究旨在探究小鼠关节软骨中IHH和PTHrP的细胞起源、定位、表达调控及假定功能。
我们在等位基因PTHrP-LacZ敲入小鼠和多个版本的PTHrP基因敲除小鼠中评估了IHH和PTHrP的表达。对选定关节进行手术卸载,以检查PTHrP和IHH的负荷诱导情况。
胚胎生长区似乎是表达PTHrP的增殖性软骨细胞的来源,这些细胞同时填充正在形成的关节软骨和生长板结构。在关节软骨中,这些细胞在中层以关节软骨细胞的形式存在。在PTHrP基因敲除小鼠中,矿化软骨细胞侵入发育中的关节软骨,但似乎因IHH驱动的表面软骨细胞增殖而无法使关节间隙矿化。在生长中和成年小鼠中,关节软骨细胞中的PTHrP表达受负荷诱导,卸载与PTHrP表达及关节软骨细胞分化的快速变化相关。
我们得出结论,IHH-PTHrP轴参与关节软骨的维持。该系统失调可能导致关节炎的发病机制。