Functional Heterogeneity Within Osteoclast Populations-a Critical Review of Four Key Publications that May Change the Paradigm of Osteoclasts.


Journal

Current osteoporosis reports
ISSN: 1544-2241
Titre abrégé: Curr Osteoporos Rep
Pays: United States
ID NLM: 101176492

Informations de publication

Date de publication:
10 2022
Historique:
accepted: 26 06 2022
pubmed: 16 7 2022
medline: 4 10 2022
entrez: 15 7 2022
Statut: ppublish

Résumé

In this review, we critically evaluate the literature for osteoclast heterogeneity, including heterogeneity in osteoclast behavior, which has hitherto been unstudied and has only recently come to attention. We give a critical review centered on four recent high-impact papers on this topic and aim to shed light on the elusive biology of osteoclasts and focus on the variant features of osteoclasts that diverge from the classical viewpoint. Osteoclasts originate from the myeloid lineage and are best known for their unique ability to resorb bone. For decades, osteoclasts have been defined simply as multinucleated cells positive for tartrate-resistant acid phosphatase activity and quantified relative to the bone perimeter or surface in histomorphometric analyses. However, several recent, high-profile studies have demonstrated the existence of heterogeneous osteoclast populations, with variable origins and functions depending on the microenvironment. This includes long-term persisting osteoclasts, inflammatory osteoclasts, recycling osteoclasts (osteomorphs), and bone resorption modes. Most of these findings have been revealed through murine studies and have helped identify new targets for human studies. These studies have also uncovered distinct sets of behavioral patterns in heterogeneous osteoclast cultures. The underlying osteoclast heterogeneity likely drives differences in bone remodeling, altering patient risk for osteoporosis and fracture. Thus, identifying the underlying key features of osteoclast heterogeneity may help in better targeting bone diseases.

Identifiants

pubmed: 35838878
doi: 10.1007/s11914-022-00738-7
pii: 10.1007/s11914-022-00738-7
doi:

Substances chimiques

Tartrate-Resistant Acid Phosphatase EC 3.1.3.2

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

344-355

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR077538
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG075227
Pays : United States
Organisme : NIAMS NIH HHS
ID : R61 AR078073
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR069620
Pays : United States

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Neha Sharma (N)

Clinical Cell Biology, Department of Pathology, Odense University Hospital, Odense, Denmark.
Pathology Research Unit, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Department of Molecular Medicine, University of Southern Denmark, J. B. Winsløws Vej 25, 1. Floor, 5000, Odense C, Denmark.

Megan M Weivoda (MM)

Department of Hematology, Mayo Clinic, Rochester, USA.

Kent Søe (K)

Clinical Cell Biology, Department of Pathology, Odense University Hospital, Odense, Denmark. Kent.soee@rsyd.dk.
Pathology Research Unit, Department of Clinical Research, University of Southern Denmark, Odense, Denmark. Kent.soee@rsyd.dk.
Department of Molecular Medicine, University of Southern Denmark, J. B. Winsløws Vej 25, 1. Floor, 5000, Odense C, Denmark. Kent.soee@rsyd.dk.

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Classifications MeSH