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Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease

PURPOSE OF REVIEW: Inflammasomes are multimeric protein structures with crucial roles in host responses against infections and injuries. The importance of inflammasome activation goes beyond host defense as a dysregulated inflammasome and subsequent secretion of IL-1 family members is believed to be...

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Autores principales: Tseng, Hsu-Wen, Samuel, Selwin Gabriel, Schroder, Kate, Lévesque, Jean-Pierre, Alexander, Kylie A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209354/
https://www.ncbi.nlm.nih.gov/pubmed/35567665
http://dx.doi.org/10.1007/s11914-022-00729-8
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author Tseng, Hsu-Wen
Samuel, Selwin Gabriel
Schroder, Kate
Lévesque, Jean-Pierre
Alexander, Kylie A
author_facet Tseng, Hsu-Wen
Samuel, Selwin Gabriel
Schroder, Kate
Lévesque, Jean-Pierre
Alexander, Kylie A
author_sort Tseng, Hsu-Wen
collection PubMed
description PURPOSE OF REVIEW: Inflammasomes are multimeric protein structures with crucial roles in host responses against infections and injuries. The importance of inflammasome activation goes beyond host defense as a dysregulated inflammasome and subsequent secretion of IL-1 family members is believed to be involved in the pathogenesis of various diseases, some of which also produce skeletal manifestations. The purpose of this review is to summarize recent developments in the understanding of inflammasome regulation and IL-1 family members in bone physiology and pathology and current therapeutics will be discussed. RECENT FINDINGS: Small animal models have been vital to help understand how the inflammasome regulates bone dynamics. Animal models with gain or loss of function in various inflammasome components or IL-1 family signaling have illustrated how these systems can impact numerous bone pathologies and have been utilized to test new inflammasome therapeutics. SUMMARY: It is increasingly clear that a tightly regulated inflammasome is required not only for host defense but for skeletal homeostasis, as a dysregulated inflammasome is linked to diseases of pathological bone accrual and loss. Given the complexities of inflammasome activation and redundancies in IL-1 activation and secretion, targeting these pathways is at times challenging. Ongoing research into inflammasome-mediated mechanisms will allow the development of new therapeutics for inflammasome/IL-1 diseases.
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spelling pubmed-92093542022-06-22 Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease Tseng, Hsu-Wen Samuel, Selwin Gabriel Schroder, Kate Lévesque, Jean-Pierre Alexander, Kylie A Curr Osteoporos Rep Osteoimmunology (A Pettit and J Charles, Section Editors) PURPOSE OF REVIEW: Inflammasomes are multimeric protein structures with crucial roles in host responses against infections and injuries. The importance of inflammasome activation goes beyond host defense as a dysregulated inflammasome and subsequent secretion of IL-1 family members is believed to be involved in the pathogenesis of various diseases, some of which also produce skeletal manifestations. The purpose of this review is to summarize recent developments in the understanding of inflammasome regulation and IL-1 family members in bone physiology and pathology and current therapeutics will be discussed. RECENT FINDINGS: Small animal models have been vital to help understand how the inflammasome regulates bone dynamics. Animal models with gain or loss of function in various inflammasome components or IL-1 family signaling have illustrated how these systems can impact numerous bone pathologies and have been utilized to test new inflammasome therapeutics. SUMMARY: It is increasingly clear that a tightly regulated inflammasome is required not only for host defense but for skeletal homeostasis, as a dysregulated inflammasome is linked to diseases of pathological bone accrual and loss. Given the complexities of inflammasome activation and redundancies in IL-1 activation and secretion, targeting these pathways is at times challenging. Ongoing research into inflammasome-mediated mechanisms will allow the development of new therapeutics for inflammasome/IL-1 diseases. Springer US 2022-05-14 2022 /pmc/articles/PMC9209354/ /pubmed/35567665 http://dx.doi.org/10.1007/s11914-022-00729-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Osteoimmunology (A Pettit and J Charles, Section Editors)
Tseng, Hsu-Wen
Samuel, Selwin Gabriel
Schroder, Kate
Lévesque, Jean-Pierre
Alexander, Kylie A
Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title_full Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title_fullStr Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title_full_unstemmed Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title_short Inflammasomes and the IL-1 Family in Bone Homeostasis and Disease
title_sort inflammasomes and the il-1 family in bone homeostasis and disease
topic Osteoimmunology (A Pettit and J Charles, Section Editors)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209354/
https://www.ncbi.nlm.nih.gov/pubmed/35567665
http://dx.doi.org/10.1007/s11914-022-00729-8
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