Martin T John, Sims Natalie A
Department of Medicine at St. Vincent's Hospital, St. Vincent's Institute of Medical Research and The University of Melbourne, 9 Princes St, Fitzroy, VIC, 3065, Australia,
Rev Endocr Metab Disord. 2015 Jun;16(2):131-9. doi: 10.1007/s11154-014-9308-6.
After it was proposed that the osteoblast lineage controlled the formation of osteoclasts, cell culture methods were developed that established this to be the case. Evidence was obtained that cytokines and hormones that promote osteoclast formation act first on osteoblast lineage cells to promote the production of a membrane-bound regulator of osteoclastogenesis. This proved to be receptor activator of NF-kB ligand (RANKL) a member of the tumor necrosis factor ligand family that acts upon its receptor RANK in the hematopoietic lineage, with interaction restricted by a decoy soluble receptor osteoprotegerin (OPG), also a product of the osteoblast lineage. The physiological roles of these factors were established through genetic and pharmacological studies, have led to a new physiology of bone, with complete revision of older ideas over the last 15 years, ultimately leading to the development of new pharmaceutical agents for bone disease.
在有人提出成骨细胞谱系控制破骨细胞形成之后,人们开发了细胞培养方法来证实确实如此。有证据表明,促进破骨细胞形成的细胞因子和激素首先作用于成骨细胞谱系细胞,以促进一种破骨细胞生成的膜结合调节因子的产生。事实证明,这就是核因子κB受体活化因子配体(RANKL),它是肿瘤坏死因子配体家族的一员,作用于造血谱系中的其受体RANK,而这种相互作用受到一种诱饵可溶性受体骨保护素(OPG)的限制,骨保护素也是成骨细胞谱系的产物。这些因子的生理作用通过基因和药理学研究得以确立,带来了骨生理学的新进展,在过去15年里对旧观念进行了全面修订,最终促成了用于治疗骨病的新型药物的研发。