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Role of Gut Microbiota in the Skeletal Response to PTH

Exposed surfaces of mammals are colonized with 100 trillion indigenous bacteria, fungi, and viruses, creating a diverse ecosystem known as the human microbiome. The gut microbiome is the richest microbiome and is now known to regulate postnatal skeletal development and the activity of the major endo...

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Detalles Bibliográficos
Autor principal: Pacifici, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947780/
https://www.ncbi.nlm.nih.gov/pubmed/33254225
http://dx.doi.org/10.1210/clinem/dgaa895
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author Pacifici, Roberto
author_facet Pacifici, Roberto
author_sort Pacifici, Roberto
collection PubMed
description Exposed surfaces of mammals are colonized with 100 trillion indigenous bacteria, fungi, and viruses, creating a diverse ecosystem known as the human microbiome. The gut microbiome is the richest microbiome and is now known to regulate postnatal skeletal development and the activity of the major endocrine regulators of bone. Parathyroid hormone (PTH) is one of the bone-regulating hormone that requires elements of the gut microbiome to exert both its bone catabolic and its bone anabolic effects. How the gut microbiome regulates the skeletal response to PTH is object of intense research. Involved mechanisms include absorption and diffusion of bacterial metabolites, such as short-chain fatty acids, and trafficking of immune cells from the gut to the bone marrow. This review will focus on how the gut microbiome communicates and regulates bone marrow cells in order to modulate the skeletal effects of PTH.
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spelling pubmed-79477802021-03-16 Role of Gut Microbiota in the Skeletal Response to PTH Pacifici, Roberto J Clin Endocrinol Metab Mini-Reviews Exposed surfaces of mammals are colonized with 100 trillion indigenous bacteria, fungi, and viruses, creating a diverse ecosystem known as the human microbiome. The gut microbiome is the richest microbiome and is now known to regulate postnatal skeletal development and the activity of the major endocrine regulators of bone. Parathyroid hormone (PTH) is one of the bone-regulating hormone that requires elements of the gut microbiome to exert both its bone catabolic and its bone anabolic effects. How the gut microbiome regulates the skeletal response to PTH is object of intense research. Involved mechanisms include absorption and diffusion of bacterial metabolites, such as short-chain fatty acids, and trafficking of immune cells from the gut to the bone marrow. This review will focus on how the gut microbiome communicates and regulates bone marrow cells in order to modulate the skeletal effects of PTH. Oxford University Press 2020-12-01 /pmc/articles/PMC7947780/ /pubmed/33254225 http://dx.doi.org/10.1210/clinem/dgaa895 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Mini-Reviews
Pacifici, Roberto
Role of Gut Microbiota in the Skeletal Response to PTH
title Role of Gut Microbiota in the Skeletal Response to PTH
title_full Role of Gut Microbiota in the Skeletal Response to PTH
title_fullStr Role of Gut Microbiota in the Skeletal Response to PTH
title_full_unstemmed Role of Gut Microbiota in the Skeletal Response to PTH
title_short Role of Gut Microbiota in the Skeletal Response to PTH
title_sort role of gut microbiota in the skeletal response to pth
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947780/
https://www.ncbi.nlm.nih.gov/pubmed/33254225
http://dx.doi.org/10.1210/clinem/dgaa895
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