Tsiridis Eleftherios, Giannoudis Peter V
Trauma & Orthopaedic Surgery, School of Medicine, University of Leeds, and St. James's University Hospital, Beckett Street, Leeds LS9 7TF, UK.
Injury. 2006 Apr;37 Suppl 1:S13-9. doi: 10.1016/j.injury.2006.02.036. Epub 2006 Apr 17.
Fracture healing is a complex physiological post-natal process, which involves the coordination of several different cell types. Exploring the orchestration of events and the simultaneous activation of osteogenesis and chondrogenesis that recapitulates mammalian embryological skeletal development seems to be not only sophisticated but also challenging. A large number of genes involved in the above process are known, but many more remain to be discovered. The functional characterisation of these genes promises to elucidate the repair process as well as skeletal abnormalities and aging. We here review the current knowledge on early and late gene expression during fracture healing, the genes so far associated with osteoblast and osteoclast differentiation, the BMP antagonists, and the Wnts signalling pathway.
骨折愈合是一个复杂的出生后生理过程,涉及多种不同细胞类型的协调。探索事件的编排以及成骨和软骨生成的同时激活,以重现哺乳动物胚胎骨骼发育,这似乎不仅复杂,而且具有挑战性。已知大量参与上述过程的基因,但仍有更多基因有待发现。这些基因的功能表征有望阐明修复过程以及骨骼异常和衰老。我们在此回顾关于骨折愈合过程中早期和晚期基因表达、目前与成骨细胞和破骨细胞分化相关的基因、骨形态发生蛋白(BMP)拮抗剂以及Wnt信号通路的现有知识。