Piters Elke, Boudin Eveline, Van Hul Wim
Department of Medical Genetics, University and University Hospital Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.
Arch Biochem Biophys. 2008 May 15;473(2):112-6. doi: 10.1016/j.abb.2008.03.006. Epub 2008 Mar 14.
Wnt signaling plays a central role in many processes during embryonic development and in later stages of life. At least three distinct wnt signaling pathways have been described. In 2001, evidence was obtained from genetic studies on some rare hereditary conditions, that the canonical wnt signaling pathway plays an important role in bone formation. Functional studies and experimental analysis of relevant animal models confirmed the anabolic effect of wnt signaling by modulating the differentiation, the proliferation, the activity and finally the apoptosis of (pre)osteoblasts and osteocytes. More recently, also non-canonical wnt signaling was shown to play a role in bone formation. Since there is currently a major lack of anabolic therapeutic agents for the prevention and treatment of osteoporosis this signaling pathway deserves major attention. A big concern, however, is the pleiotropic function of the pathway that needs to be taken into account in order to avoid unwanted side-effects. Preliminary data are already indicating that this might be achieved by targeting sclerostin, a bone-specific extracellular antagonist of canonical wnt signaling.
Wnt信号通路在胚胎发育的许多过程以及生命后期阶段发挥着核心作用。至少已描述了三种不同的Wnt信号通路。2001年,通过对一些罕见遗传性疾病的基因研究获得证据,表明经典Wnt信号通路在骨形成中起重要作用。相关动物模型的功能研究和实验分析证实,Wnt信号通路通过调节(前)成骨细胞和骨细胞的分化、增殖、活性以及最终的凋亡发挥合成代谢作用。最近,非经典Wnt信号通路也被证明在骨形成中起作用。由于目前严重缺乏用于预防和治疗骨质疏松症的合成代谢治疗药物,该信号通路值得高度关注。然而,一个重大问题是该通路的多效性功能,为避免不必要的副作用需要加以考虑。初步数据已表明,这可能通过靶向硬化蛋白来实现,硬化蛋白是经典Wnt信号通路的一种骨特异性细胞外拮抗剂。