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Ostm1 from Mouse to Human: Insights into Osteoclast Maturation

The maintenance of bone mass is a dynamic process that requires a strict balance between bone formation and resorption. Bone formation is controlled by osteoblasts, while osteoclasts are responsible for resorption of the bone matrix. The opposite functions of these cell types have to be tightly regu...

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Detalles Bibliográficos
Autores principales: Vacher, Jean, Bruccoleri, Michael, Pata, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460669/
https://www.ncbi.nlm.nih.gov/pubmed/32764302
http://dx.doi.org/10.3390/ijms21165600
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author Vacher, Jean
Bruccoleri, Michael
Pata, Monica
author_facet Vacher, Jean
Bruccoleri, Michael
Pata, Monica
author_sort Vacher, Jean
collection PubMed
description The maintenance of bone mass is a dynamic process that requires a strict balance between bone formation and resorption. Bone formation is controlled by osteoblasts, while osteoclasts are responsible for resorption of the bone matrix. The opposite functions of these cell types have to be tightly regulated not only during normal bone development, but also during adult life, to maintain serum calcium homeostasis and sustain bone integrity to prevent bone fractures. Disruption of the control of bone synthesis or resorption can lead to an over accumulation of bone tissue in osteopetrosis or conversely to a net depletion of the bone mass in osteoporosis. Moreover, high levels of bone resorption with focal bone formation can cause Paget’s disease. Here, we summarize the steps toward isolation and characterization of the osteopetrosis associated trans-membrane protein 1 (Ostm1) gene and protein, essential for proper osteoclast maturation, and responsible when mutated for the most severe form of osteopetrosis in mice and humans.
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spelling pubmed-74606692020-09-03 Ostm1 from Mouse to Human: Insights into Osteoclast Maturation Vacher, Jean Bruccoleri, Michael Pata, Monica Int J Mol Sci Review The maintenance of bone mass is a dynamic process that requires a strict balance between bone formation and resorption. Bone formation is controlled by osteoblasts, while osteoclasts are responsible for resorption of the bone matrix. The opposite functions of these cell types have to be tightly regulated not only during normal bone development, but also during adult life, to maintain serum calcium homeostasis and sustain bone integrity to prevent bone fractures. Disruption of the control of bone synthesis or resorption can lead to an over accumulation of bone tissue in osteopetrosis or conversely to a net depletion of the bone mass in osteoporosis. Moreover, high levels of bone resorption with focal bone formation can cause Paget’s disease. Here, we summarize the steps toward isolation and characterization of the osteopetrosis associated trans-membrane protein 1 (Ostm1) gene and protein, essential for proper osteoclast maturation, and responsible when mutated for the most severe form of osteopetrosis in mice and humans. MDPI 2020-08-05 /pmc/articles/PMC7460669/ /pubmed/32764302 http://dx.doi.org/10.3390/ijms21165600 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vacher, Jean
Bruccoleri, Michael
Pata, Monica
Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title_full Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title_fullStr Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title_full_unstemmed Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title_short Ostm1 from Mouse to Human: Insights into Osteoclast Maturation
title_sort ostm1 from mouse to human: insights into osteoclast maturation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460669/
https://www.ncbi.nlm.nih.gov/pubmed/32764302
http://dx.doi.org/10.3390/ijms21165600
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