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Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption
Author(s) -
Michelle M. McDonald,
Weng Hua Khoo,
Pei Ying Ng,
Ya Xiao,
Jad Zamerli,
Peter Thatcher,
Wunna Kyaw,
Karrnan Pathmanandavel,
Abigail K. Grootveld,
Imogen Moran,
Danyal Butt,
Akira Nguyen,
Alexander P. Corr,
Sean Warren,
Maté Biro,
Natalie C. Butterfield,
Siobhan E. Guilfoyle,
Davide KomlaEbri,
Michael R.G. Dack,
Hannah F. Dewhurst,
John G. Logan,
Yongxiao Li,
Sindhu T. Mohanty,
Niall M. Byrne,
Rachael Terry,
Marija K. Simic,
Ryan C. Chai,
Julian M.W. Quinn,
Scott E. Youlten,
Jessica A. Pettitt,
David AbiHanna,
Rohit Jain,
Wolfgang Weninger,
Mischa Lundberg,
Shuting Sun,
Frank H. Ebetino,
Paul Timpson,
Woei Ming Lee,
Paul A. Baldock,
Michael J. Rogers,
Robert Brink,
Graham R. Williams,
J. H. Duncan Bassett,
John P. Kemp,
Nathan J. Pavlos,
Peter I. Croucher,
Tri Giang Phan
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2021.02.002
Subject(s) - rankl , multinucleate , osteoclast , bone resorption , biology , microbiology and biotechnology , resorption , macrophage colony stimulating factor , phenotype , macrophage , gene , endocrinology , genetics , receptor , in vitro , activator (genetics)
Summary Osteoclasts are large multinucleated bone-resorbing cells formed by the fusion of monocyte/macrophage-derived precursors that are thought to undergo apoptosis once resorption is complete. Here, by intravital imaging, we reveal that RANKL-stimulated osteoclasts have an alternative cell fate in which they fission into daughter cells called osteomorphs. Inhibiting RANKL blocked this cellular recycling and resulted in osteomorph accumulation. Single-cell RNA sequencing showed that osteomorphs are transcriptionally distinct from osteoclasts and macrophages and express a number of non-canonical osteoclast genes that are associated with structural and functional bone phenotypes when deleted in mice. Furthermore, genetic variation in human orthologs of osteomorph genes causes monogenic skeletal disorders and associates with bone mineral density, a polygenetic skeletal trait. Thus, osteoclasts recycle via osteomorphs, a cell type involved in the regulation of bone resorption that may be targeted for the treatment of skeletal diseases.

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