Vortkamp A
Max-Planck-Insitut für Molekulare Genetik, Berlin, Germany.
Osteoarthritis Cartilage. 2001;9 Suppl A:S109-17.
Endochondral ossification is multistep process that is regulated by a complex network of signalling systems. Endochondral ossification is initiated with the condensation of chondrocytes into cartilage elements in which the chondrocytes subsequently progress through stages of proliferation and hypertrophic differentiation. Finally, terminally differentiated chondrocytes undergo apoptosis and are replaced by bone. As hypertrophic differentiation links chondrocyte proliferation with the ossification of the skeletal elements it seems to be one of the critical steps in this process (Fig. 5). Ihh and PTHrP are two signalling molecules that interact in a negative feedback loop regulating the pace of hypertrophic differentiation. In addition Ihh has recently been shown to independently regulate chondrocyte proliferation and the ossification process, thus coordinating three different steps of endochondral bone formation. Two other groups of signalling molecules have been found to interact with Ihh during endochondral ossification. BMP signalling seems to act downstream of Ihh. BMPs might serve as secondary signals downstream of Ihh mediating the Ihh signals to the periarticular perichondrium to induce PTHrP. Alternatively BMP signalling, induced by Ihh, might reciprocally act back on the prehypertrophic chondrocytes, thereby coordinating hypertrophic differentiation with the differentiation of the periosteum. The idea of an interaction of the two signalling systems is supported by the fact that not only BMPs but also their receptors and at least two of the BMP antagonist are expressed in regions that are thought to be targets of Ihh signalling. A third signalling pathway critical for proper bone development is signalling through the FGFR3, which seem to act upstream of both Ihh and BMP signalling. In summary, it becomes more and more obvious that the single steps of endochondral ossification are tightly coordinated. For example signals from the joint region of the cartilage elements play an important role in regulating both chondrocyte proliferation and differentiation and at least some of these signals seem to interact with signals from the hypertrophic region, linking hypertrophic differentiation and proliferation. In addition, signals from the perichondrium/periosteum are thought to interact with signals from the differentiating chondrocytes to coordinate the differentiation of the periosteum with hypertrophic differentiation. Although significant progress has been made during the last years in analysing the signals regulating endochondral ossification in the developing embryo, complete understanding of the control system will require further extensive studies.
软骨内成骨是一个多步骤的过程,受复杂信号系统网络的调控。软骨内成骨始于软骨细胞凝聚形成软骨元件,其中软骨细胞随后经历增殖和肥大分化阶段。最后,终末分化的软骨细胞发生凋亡并被骨组织取代。由于肥大分化将软骨细胞增殖与骨骼元件的骨化联系起来,它似乎是这一过程中的关键步骤之一(图5)。Ihh和甲状旁腺激素相关蛋白(PTHrP)是在负反馈回路中相互作用以调节肥大分化进程的两种信号分子。此外,最近研究表明Ihh可独立调节软骨细胞增殖和骨化过程,从而协调软骨内骨形成的三个不同步骤。在软骨内成骨过程中还发现另外两组信号分子与Ihh相互作用。骨形态发生蛋白(BMP)信号似乎在Ihh下游起作用。BMP可能作为Ihh下游的二级信号,将Ihh信号传递至关节周围软骨膜以诱导PTHrP。或者,由Ihh诱导的BMP信号可能反过来作用于前肥大软骨细胞,从而协调肥大分化与骨膜分化。两个信号系统相互作用的观点得到以下事实的支持:不仅BMP及其受体,而且至少两种BMP拮抗剂在被认为是Ihh信号靶标的区域表达。对正常骨骼发育至关重要的第三条信号通路是通过成纤维细胞生长因子受体3(FGFR3)的信号传导,它似乎在Ihh和BMP信号传导的上游起作用。总之,越来越明显的是,软骨内成骨的各个步骤紧密协调。例如,来自软骨元件关节区域的信号在调节软骨细胞增殖和分化方面发挥重要作用,并且这些信号中至少有一些似乎与来自肥大区域的信号相互作用,将肥大分化与增殖联系起来。此外,软骨膜/骨膜的信号被认为与分化中的软骨细胞的信号相互作用,以协调骨膜分化与肥大分化。尽管在过去几年中,在分析发育胚胎中调节软骨内成骨的信号方面取得了重大进展,但要完全理解控制系统仍需要进一步广泛的研究。