Common signalling pathways in macrophage and osteoclast multinucleation
Author(s) -
Marie Pereira,
Enrico Petretto,
Siamon Gordon,
J. H. Duncan Bassett,
Graham R. Williams,
Jacques Behmoaras
Publication year - 2018
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.216267
Subject(s) - giant cell , multinucleate , biology , osteoclast , cell fusion , bone resorption , macrophage , foreign body giant cell , syncytium , pathogenesis , microbiology and biotechnology , immunology , pathology , cell , genetics , medicine , receptor , in vitro
Macrophage cell fusion and multinucleation are fundamental processes in the formation of multinucleated giant cells (MGCs) in chronic inflammatory disease and osteoclasts in the regulation of bone mass. However, this basic cell phenomenon is poorly understood despite its pathophysiological relevance. Granulomas containing multinucleated giant cells are seen in a wide variety of complex inflammatory disorders, as well as in infectious diseases. Dysregulation of osteoclastic bone resorption underlies the pathogenesis of osteoporosis and malignant osteolytic bone disease. Recent reports have shown that the formation of multinucleated giant cells and osteoclast fusion display a common molecular signature, suggesting shared genetic determinants. In this Review, we describe the background of cell-cell fusion and the similar origin of macrophages and osteoclasts. We specifically focus on the common pathways involved in osteoclast and MGC fusion. We also highlight potential approaches that could help to unravel the core mechanisms underlying bone and granulomatous disorders in humans.
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