Common signalling pathways in macrophage and osteoclast multinucleation
File(s)Pereira et al, JCS accepted version.pdf (942.39 KB)
Accepted version
Author(s)
Type
Journal Article
Abstract
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.
Date Issued
2018-06-05
Date Acceptance
2018-04-16
Citation
Journal of Cell Science, 2018, 131 (11)
ISSN
0021-9533
Publisher
Company of Biologists
Journal / Book Title
Journal of Cell Science
Volume
131
Issue
11
Copyright Statement
© 2018. Published by The Company of Biologists Ltd
Sponsor
Medical Research Council (MRC)
Medical Research Council (MRC)
Grant Number
MR/M004716/1
MR/N01121X/1
Subjects
Science & Technology
Life Sciences & Biomedicine
Cell Biology
fusion
Macrophages
Multinucleation
Osteoclasts
GIANT-CELL FORMATION
COLONY-STIMULATING FACTOR
TUMOR-NECROSIS-FACTOR
MOUSE BONE-MARROW
GRANULOMA-FORMATION
DENDRITIC CELLS
FACTOR-I
MYCOBACTERIUM-TUBERCULOSIS
ALPHA-V-BETA-3 INTEGRIN
MONONUCLEAR PHAGOCYTES
Cell fusion
06 Biological Sciences
11 Medical And Health Sciences
Developmental Biology
Publication Status
Published