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Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host
Inflammation has a role in the pathogenesis of childhood malnutrition. We investigated the effect of malnutrition and inflammatory challenge on bone marrow composition and bone health. We studied an established murine model of moderate acute malnutrition at baseline and after acute inflammatory chal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380851/ https://www.ncbi.nlm.nih.gov/pubmed/35983045 http://dx.doi.org/10.3389/fimmu.2022.846246 |
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author | Osorio, E. Yaneth Gugala, Zbigniew Patterson, Grace T. Palacios, Genesis Cordova, Erika Uscanga-Palomeque, Ashanti Travi, Bruno L. Melby, Peter C. |
author_facet | Osorio, E. Yaneth Gugala, Zbigniew Patterson, Grace T. Palacios, Genesis Cordova, Erika Uscanga-Palomeque, Ashanti Travi, Bruno L. Melby, Peter C. |
author_sort | Osorio, E. Yaneth |
collection | PubMed |
description | Inflammation has a role in the pathogenesis of childhood malnutrition. We investigated the effect of malnutrition and inflammatory challenge on bone marrow composition and bone health. We studied an established murine model of moderate acute malnutrition at baseline and after acute inflammatory challenge with bacterial lipopolysaccharide (LPS), a surrogate of Gram-negative bacterial sepsis, or Leishmania donovani, the cause of visceral leishmaniasis. Both of these infections cause significant morbidity and mortality in malnourished children. Of the 2 stimuli, LPS caused more pronounced bone marrow changes that were amplified in malnourished mice. LPS challenge led to increased inflammatory cytokine expression (Il1b, Il6, and Tnf), inflammasome activation, and inflammatory monocyte accumulation in the bone marrow of malnourished mice. Depletion of inflammatory monocytes in Csfr1-LysMcre-DT malnourished mice significantly reduced the inflammasome activation and IL1-ß production after LPS challenge. The inflammatory challenge also led to increased expansion of mesenchymal stem cells (MSCs), bone marrow adiposity, and expression of genes (Pparg, Adipoq, and Srbp1) associated with adipogenesis in malnourished mice. This suggests that inflammatory challenge promotes differentiation of BM MSCs toward the adipocyte lineage rather than toward bone-forming osteoblasts in the malnourished host. Concurrent with this reduced osteoblastic potential there was an increase in bone-resorbing osteoclasts, enhanced osteoclast activity, upregulation of inflammatory genes, and IL-1B involved in osteoclast differentiation and activation. The resulting weakened bone formation and increased bone resorption would contribute to the bone fragility associated with malnutrition. Lastly, we evaluated the effect of replacing lipid rich in omega-6 fatty acids (corn oil) with lipid-rich in omega-3 fatty acids (fish oil) in the nutrient-deficient diet. LPS-challenged malnourished mice that received dietary fish oil showed decreased expression of inflammatory cytokines and Rankl and reduced osteoclast differentiation and activation in the bone marrow. This work demonstrates that the negative effect of inflammatory challenge on bone marrow is amplified in the malnourished host. Increasing dietary intake of omega-3 fatty acids may be a means to reduce inflammation and improve bone health in malnourished children. |
format | Online Article Text |
id | pubmed-9380851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93808512022-08-17 Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host Osorio, E. Yaneth Gugala, Zbigniew Patterson, Grace T. Palacios, Genesis Cordova, Erika Uscanga-Palomeque, Ashanti Travi, Bruno L. Melby, Peter C. Front Immunol Immunology Inflammation has a role in the pathogenesis of childhood malnutrition. We investigated the effect of malnutrition and inflammatory challenge on bone marrow composition and bone health. We studied an established murine model of moderate acute malnutrition at baseline and after acute inflammatory challenge with bacterial lipopolysaccharide (LPS), a surrogate of Gram-negative bacterial sepsis, or Leishmania donovani, the cause of visceral leishmaniasis. Both of these infections cause significant morbidity and mortality in malnourished children. Of the 2 stimuli, LPS caused more pronounced bone marrow changes that were amplified in malnourished mice. LPS challenge led to increased inflammatory cytokine expression (Il1b, Il6, and Tnf), inflammasome activation, and inflammatory monocyte accumulation in the bone marrow of malnourished mice. Depletion of inflammatory monocytes in Csfr1-LysMcre-DT malnourished mice significantly reduced the inflammasome activation and IL1-ß production after LPS challenge. The inflammatory challenge also led to increased expansion of mesenchymal stem cells (MSCs), bone marrow adiposity, and expression of genes (Pparg, Adipoq, and Srbp1) associated with adipogenesis in malnourished mice. This suggests that inflammatory challenge promotes differentiation of BM MSCs toward the adipocyte lineage rather than toward bone-forming osteoblasts in the malnourished host. Concurrent with this reduced osteoblastic potential there was an increase in bone-resorbing osteoclasts, enhanced osteoclast activity, upregulation of inflammatory genes, and IL-1B involved in osteoclast differentiation and activation. The resulting weakened bone formation and increased bone resorption would contribute to the bone fragility associated with malnutrition. Lastly, we evaluated the effect of replacing lipid rich in omega-6 fatty acids (corn oil) with lipid-rich in omega-3 fatty acids (fish oil) in the nutrient-deficient diet. LPS-challenged malnourished mice that received dietary fish oil showed decreased expression of inflammatory cytokines and Rankl and reduced osteoclast differentiation and activation in the bone marrow. This work demonstrates that the negative effect of inflammatory challenge on bone marrow is amplified in the malnourished host. Increasing dietary intake of omega-3 fatty acids may be a means to reduce inflammation and improve bone health in malnourished children. Frontiers Media S.A. 2022-08-02 /pmc/articles/PMC9380851/ /pubmed/35983045 http://dx.doi.org/10.3389/fimmu.2022.846246 Text en Copyright © 2022 Osorio, Gugala, Patterson, Palacios, Cordova, Uscanga-Palomeque, Travi and Melby https://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 Osorio, E. Yaneth Gugala, Zbigniew Patterson, Grace T. Palacios, Genesis Cordova, Erika Uscanga-Palomeque, Ashanti Travi, Bruno L. Melby, Peter C. Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title | Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title_full | Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title_fullStr | Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title_full_unstemmed | Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title_short | Inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
title_sort | inflammatory stimuli alter bone marrow composition and compromise bone health in the malnourished host |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380851/ https://www.ncbi.nlm.nih.gov/pubmed/35983045 http://dx.doi.org/10.3389/fimmu.2022.846246 |
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