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Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing

Bone formation as well as bone healing capacity is known to be impaired in the elderly. Although bone formation is outpaced by bone resorption in aged individuals, we hereby present a novel path that considerably impacts bone formation and architecture: Bone formation is substantially reduced in age...

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Autores principales: Bucher, Christian H., Schlundt, Claudia, Wulsten, Dag, Sass, F. Andrea, Wendler, Sebastian, Ellinghaus, Agnes, Thiele, Tobias, Seemann, Ricarda, Willie, Bettina M., Volk, Hans-Dieter, Duda, Georg N., Schmidt-Bleek, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474158/
https://www.ncbi.nlm.nih.gov/pubmed/31031773
http://dx.doi.org/10.3389/fimmu.2019.00797
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author Bucher, Christian H.
Schlundt, Claudia
Wulsten, Dag
Sass, F. Andrea
Wendler, Sebastian
Ellinghaus, Agnes
Thiele, Tobias
Seemann, Ricarda
Willie, Bettina M.
Volk, Hans-Dieter
Duda, Georg N.
Schmidt-Bleek, Katharina
author_facet Bucher, Christian H.
Schlundt, Claudia
Wulsten, Dag
Sass, F. Andrea
Wendler, Sebastian
Ellinghaus, Agnes
Thiele, Tobias
Seemann, Ricarda
Willie, Bettina M.
Volk, Hans-Dieter
Duda, Georg N.
Schmidt-Bleek, Katharina
author_sort Bucher, Christian H.
collection PubMed
description Bone formation as well as bone healing capacity is known to be impaired in the elderly. Although bone formation is outpaced by bone resorption in aged individuals, we hereby present a novel path that considerably impacts bone formation and architecture: Bone formation is substantially reduced in aged individual owing to the experience of the adaptive immunity. Thus, immune-aging in addition to chronological aging is a potential risk factor, with an experienced immune system being recognized as more pro-inflammatory. The role of the aging immune system on bone homeostasis and on the bone healing cascade has so far not been considered. Within this study mice at different age and immunological experience were analyzed toward bone properties. Healing was assessed by introducing an osteotomy, immune cells were adoptively transferred to disclose the difference in biological vs. chronological aging. In vitro studies were employed to test the interaction of immune cell products (cytokines) on cells of the musculoskeletal system. In metaphyseal bone, immune-aging affects bone homeostasis by impacting bone formation capacity and thereby influencing mass and microstructure of bone trabeculae leading to an overall reduced mechanical competence as found in bone torsional testing. Furthermore, bone formation is also impacted during bone regeneration in terms of a diminished healing capacity observed in young animals who have an experienced human immune system. We show the impact of an experienced immune system compared to a naïve immune system, demonstrating the substantial differences in the healing capacity and bone homeostasis due to the immune composition. We further showed that in vivo mechanical stimulation changed the immune system phenotype in young mice toward a more naïve composition. While this rescue was found to be significant in young individuals, aged mice only showed a trend toward the reconstitution of a more naïve immune phenotype. Considering the immune system's experience level in an individual, will likely allow one to differentiate (stratify) and treat (immune-modulate) patients more effectively. This work illustrates the relevance of including immune diagnostics when discussing immunomodulatory therapeutic strategies for the progressively aging population of the industrial countries.
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spelling pubmed-64741582019-04-26 Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing Bucher, Christian H. Schlundt, Claudia Wulsten, Dag Sass, F. Andrea Wendler, Sebastian Ellinghaus, Agnes Thiele, Tobias Seemann, Ricarda Willie, Bettina M. Volk, Hans-Dieter Duda, Georg N. Schmidt-Bleek, Katharina Front Immunol Immunology Bone formation as well as bone healing capacity is known to be impaired in the elderly. Although bone formation is outpaced by bone resorption in aged individuals, we hereby present a novel path that considerably impacts bone formation and architecture: Bone formation is substantially reduced in aged individual owing to the experience of the adaptive immunity. Thus, immune-aging in addition to chronological aging is a potential risk factor, with an experienced immune system being recognized as more pro-inflammatory. The role of the aging immune system on bone homeostasis and on the bone healing cascade has so far not been considered. Within this study mice at different age and immunological experience were analyzed toward bone properties. Healing was assessed by introducing an osteotomy, immune cells were adoptively transferred to disclose the difference in biological vs. chronological aging. In vitro studies were employed to test the interaction of immune cell products (cytokines) on cells of the musculoskeletal system. In metaphyseal bone, immune-aging affects bone homeostasis by impacting bone formation capacity and thereby influencing mass and microstructure of bone trabeculae leading to an overall reduced mechanical competence as found in bone torsional testing. Furthermore, bone formation is also impacted during bone regeneration in terms of a diminished healing capacity observed in young animals who have an experienced human immune system. We show the impact of an experienced immune system compared to a naïve immune system, demonstrating the substantial differences in the healing capacity and bone homeostasis due to the immune composition. We further showed that in vivo mechanical stimulation changed the immune system phenotype in young mice toward a more naïve composition. While this rescue was found to be significant in young individuals, aged mice only showed a trend toward the reconstitution of a more naïve immune phenotype. Considering the immune system's experience level in an individual, will likely allow one to differentiate (stratify) and treat (immune-modulate) patients more effectively. This work illustrates the relevance of including immune diagnostics when discussing immunomodulatory therapeutic strategies for the progressively aging population of the industrial countries. Frontiers Media S.A. 2019-04-12 /pmc/articles/PMC6474158/ /pubmed/31031773 http://dx.doi.org/10.3389/fimmu.2019.00797 Text en Copyright © 2019 Bucher, Schlundt, Wulsten, Sass, Wendler, Ellinghaus, Thiele, Seemann, Willie, Volk, Duda and Schmidt-Bleek. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bucher, Christian H.
Schlundt, Claudia
Wulsten, Dag
Sass, F. Andrea
Wendler, Sebastian
Ellinghaus, Agnes
Thiele, Tobias
Seemann, Ricarda
Willie, Bettina M.
Volk, Hans-Dieter
Duda, Georg N.
Schmidt-Bleek, Katharina
Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title_full Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title_fullStr Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title_full_unstemmed Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title_short Experience in the Adaptive Immunity Impacts Bone Homeostasis, Remodeling, and Healing
title_sort experience in the adaptive immunity impacts bone homeostasis, remodeling, and healing
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474158/
https://www.ncbi.nlm.nih.gov/pubmed/31031773
http://dx.doi.org/10.3389/fimmu.2019.00797
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