Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Roosevelt Drive, Oxford, OX3 7FY, UK.
Calcif Tissue Int. 2014 Jan;94(1):98-111. doi: 10.1007/s00223-013-9764-0. Epub 2013 Aug 3.
There is a complex interplay between the cells of the immune system and bone. Immune cells, such as T and NK cells, are able to enhance osteoclast formation via the production of RANKL. Yet there is increasing evidence to show that during the resolution of inflammation or as a consequence of increased osteoclastogenesis there is an anabolic response via the formation of more osteoblasts. Furthermore, osteoblasts themselves are involved in the control of immune cell function, thus promoting the resolution of inflammation. Hence, the concept of "coupling"-how bone formation is linked to resorption-needs to be more inclusive rather than restricting our focus to osteoblast-osteoclast interactions as in a whole organism these cells are never in isolation. This review will investigate the role of immune cells in normal bone homeostasis and in inflammatory diseases where the balance between resorption and formation is lost.
免疫系统细胞和骨骼之间存在着复杂的相互作用。免疫细胞,如 T 和 NK 细胞,能够通过产生 RANKL 来增强破骨细胞的形成。然而,越来越多的证据表明,在炎症的消退过程中,或者由于破骨细胞生成增加,通过形成更多的成骨细胞,会出现合成代谢反应。此外,成骨细胞本身也参与了免疫细胞功能的控制,从而促进了炎症的消退。因此,“耦联”的概念——即骨形成与吸收的联系——需要更加全面,而不是将我们的注意力仅仅局限于成骨细胞-破骨细胞的相互作用,因为在整个生物体中,这些细胞从来都不是孤立存在的。这篇综述将探讨免疫细胞在正常骨稳态和炎症性疾病中的作用,在这些疾病中,吸收和形成之间的平衡被打破了。