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Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion

Osteoclasts are myeloid lineage cells with a unique bone-destroying ability that maintains bone homeostasis together with bone formation by osteoblasts. An advanced intravital imaging system using a two-photon microscopy has enabled the observation and evaluation of osteoclast dynamics and behaviors...

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Autores principales: Agemura, Tomoya, Hasegawa, Tetsuo, Yari, Shinya, Kikuta, Junichi, Ishii, Masaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161570/
https://www.ncbi.nlm.nih.gov/pubmed/35650653
http://dx.doi.org/10.1186/s41232-022-00206-w
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author Agemura, Tomoya
Hasegawa, Tetsuo
Yari, Shinya
Kikuta, Junichi
Ishii, Masaru
author_facet Agemura, Tomoya
Hasegawa, Tetsuo
Yari, Shinya
Kikuta, Junichi
Ishii, Masaru
author_sort Agemura, Tomoya
collection PubMed
description Osteoclasts are myeloid lineage cells with a unique bone-destroying ability that maintains bone homeostasis together with bone formation by osteoblasts. An advanced intravital imaging system using a two-photon microscopy has enabled the observation and evaluation of osteoclast dynamics and behaviors in the bone marrow of living mice. Using this system, it has become clear that pathological osteoclasts under inflamed conditions differ from physiological osteoclasts under a steady-state. Recently, we identified novel osteoclast precursors in arthritis, called arthritis-associated osteoclastogenic macrophages (AtoMs), which differentiate into pathological osteoclasts and induce inflammatory bone destruction. In this review, we introduce the in vivo imaging of physiological and pathological osteoclasts and their differentiation mechanism.
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spelling pubmed-91615702022-06-03 Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion Agemura, Tomoya Hasegawa, Tetsuo Yari, Shinya Kikuta, Junichi Ishii, Masaru Inflamm Regen Review Osteoclasts are myeloid lineage cells with a unique bone-destroying ability that maintains bone homeostasis together with bone formation by osteoblasts. An advanced intravital imaging system using a two-photon microscopy has enabled the observation and evaluation of osteoclast dynamics and behaviors in the bone marrow of living mice. Using this system, it has become clear that pathological osteoclasts under inflamed conditions differ from physiological osteoclasts under a steady-state. Recently, we identified novel osteoclast precursors in arthritis, called arthritis-associated osteoclastogenic macrophages (AtoMs), which differentiate into pathological osteoclasts and induce inflammatory bone destruction. In this review, we introduce the in vivo imaging of physiological and pathological osteoclasts and their differentiation mechanism. BioMed Central 2022-06-02 /pmc/articles/PMC9161570/ /pubmed/35650653 http://dx.doi.org/10.1186/s41232-022-00206-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Agemura, Tomoya
Hasegawa, Tetsuo
Yari, Shinya
Kikuta, Junichi
Ishii, Masaru
Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title_full Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title_fullStr Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title_full_unstemmed Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title_short Arthritis-associated osteoclastogenic macrophage, AtoM, as a key player in pathological bone erosion
title_sort arthritis-associated osteoclastogenic macrophage, atom, as a key player in pathological bone erosion
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161570/
https://www.ncbi.nlm.nih.gov/pubmed/35650653
http://dx.doi.org/10.1186/s41232-022-00206-w
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