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Osteoclasts are multinucleated cells derived from mononuclear phagocyte precursors (monocytes, macrophages); in the canonical pathway of osteoclastogenesis, these cells fuse and differentiate to form specialised bone-resorbing osteoclasts in the presence of receptor activator for nuclear factor kappa B ligand (RANKL). Non-canonical pathways of osteoclastogenesis have been described in which several cytokines and growth factors are able to substitute for RANKL. These humoral factors can generally be divided into those which, like RANKL, are tumour necrosis family (TNF) superfamily members and those which are not; the former include TNFα lymphotoxin exhibiting inducible expression and competing with herpes simplex virus glycoprotein D for herpesvirus entry mediator, a receptor expressed by T lymphocytes (LIGHT), a proliferation inducing ligand (APRIL) and B cell activating factor (BAFF); the latter include transforming growth factor beta (TGF-β), interleukin-6 (IL-6), IL-8, IL-11, nerve growth factor (NGF), insulin-like growth factor-I (IGF-I) and IGF-II. This review summarises the evidence for these RANKL substitutes in inducing osteoclast differentiation from tissue-derived and circulating mononuclear phagocytes. It also assesses the role these factors are likely to play in promoting the pathological bone resorption seen in many inflammatory and neoplastic lesions of bone and joint including rheumatoid arthritis, aseptic implant loosening and primary and secondary tumours of bone.

Original publication

DOI

10.1007/s12016-015-8523-6

Type

Journal article

Journal

Clin Rev Allergy Immunol

Publication Date

08/2016

Volume

51

Pages

16 - 26

Keywords

Bone resorption, Cytokine, LIGHT, Osteoclast, RANKL, TNF, Bone Resorption, Cytokines, Humans, Multigene Family, Musculoskeletal Diseases, Osteoclasts, Protein Binding, RANK Ligand, Receptor Activator of Nuclear Factor-kappa B, Signal Transduction, Tumor Necrosis Factor Ligand Superfamily Member 14, Tumor Necrosis Factors