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Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis
Lipocalin-2 is a constituent of the neutrophil secondary granules and is expressed de novo by macrophages and epithelium in response to inflammation. Lipocalin-2 acts in a bacteriostatic fashion by binding iron-loaded siderophores required for bacterial growth. Mycobacterium tuberculosis (M.tb) prod...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275245/ https://www.ncbi.nlm.nih.gov/pubmed/30534124 http://dx.doi.org/10.3389/fimmu.2018.02717 |
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author | Dahl, Sara Louise Woodworth, Joshua S. Lerche, Christian Johann Cramer, Elisabeth Præstekjær Nielsen, Pia Rude Moser, Claus Thomsen, Allan Randrup Borregaard, Niels Cowland, Jack Bernard |
author_facet | Dahl, Sara Louise Woodworth, Joshua S. Lerche, Christian Johann Cramer, Elisabeth Præstekjær Nielsen, Pia Rude Moser, Claus Thomsen, Allan Randrup Borregaard, Niels Cowland, Jack Bernard |
author_sort | Dahl, Sara Louise |
collection | PubMed |
description | Lipocalin-2 is a constituent of the neutrophil secondary granules and is expressed de novo by macrophages and epithelium in response to inflammation. Lipocalin-2 acts in a bacteriostatic fashion by binding iron-loaded siderophores required for bacterial growth. Mycobacterium tuberculosis (M.tb) produces siderophores that can be bound by lipocalin-2. The impact of lipocalin-2 in the innate immune response toward extracellular bacteria has been established whereas the effect on intracellular bacteria, such as M.tb, is less well-described. Here we show that lipocalin-2 surprisingly confers a growth advantage on M.tb in the early stages of infection (3 weeks post-challenge). Using mixed bone marrow chimeras, we demonstrate that lipocalin-2 derived from granulocytes, but not from epithelia and macrophages, leads to increased susceptibility to M.tb infection. In contrast, lipocalin-2 is not observed to promote mycobacterial growth at later stages of M.tb infection. We demonstrate co-localization of granulocytes and mycobacteria within the nascent granulomas at week 3 post-challenge, but not in the consolidated granulomas at week 5. We hypothesize that neutrophil-derived lipocalin-2 acts to supply a source of iron to M.tb in infected macrophages within the immature granuloma, thereby facilitating mycobacterial growth. |
format | Online Article Text |
id | pubmed-6275245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62752452018-12-10 Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis Dahl, Sara Louise Woodworth, Joshua S. Lerche, Christian Johann Cramer, Elisabeth Præstekjær Nielsen, Pia Rude Moser, Claus Thomsen, Allan Randrup Borregaard, Niels Cowland, Jack Bernard Front Immunol Immunology Lipocalin-2 is a constituent of the neutrophil secondary granules and is expressed de novo by macrophages and epithelium in response to inflammation. Lipocalin-2 acts in a bacteriostatic fashion by binding iron-loaded siderophores required for bacterial growth. Mycobacterium tuberculosis (M.tb) produces siderophores that can be bound by lipocalin-2. The impact of lipocalin-2 in the innate immune response toward extracellular bacteria has been established whereas the effect on intracellular bacteria, such as M.tb, is less well-described. Here we show that lipocalin-2 surprisingly confers a growth advantage on M.tb in the early stages of infection (3 weeks post-challenge). Using mixed bone marrow chimeras, we demonstrate that lipocalin-2 derived from granulocytes, but not from epithelia and macrophages, leads to increased susceptibility to M.tb infection. In contrast, lipocalin-2 is not observed to promote mycobacterial growth at later stages of M.tb infection. We demonstrate co-localization of granulocytes and mycobacteria within the nascent granulomas at week 3 post-challenge, but not in the consolidated granulomas at week 5. We hypothesize that neutrophil-derived lipocalin-2 acts to supply a source of iron to M.tb in infected macrophages within the immature granuloma, thereby facilitating mycobacterial growth. Frontiers Media S.A. 2018-11-26 /pmc/articles/PMC6275245/ /pubmed/30534124 http://dx.doi.org/10.3389/fimmu.2018.02717 Text en Copyright © 2018 Dahl, Woodworth, Lerche, Cramer, Nielsen, Moser, Thomsen, Borregaard and Cowland. 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 Dahl, Sara Louise Woodworth, Joshua S. Lerche, Christian Johann Cramer, Elisabeth Præstekjær Nielsen, Pia Rude Moser, Claus Thomsen, Allan Randrup Borregaard, Niels Cowland, Jack Bernard Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title | Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title_full | Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title_fullStr | Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title_full_unstemmed | Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title_short | Lipocalin-2 Functions as Inhibitor of Innate Resistance to Mycobacterium tuberculosis |
title_sort | lipocalin-2 functions as inhibitor of innate resistance to mycobacterium tuberculosis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275245/ https://www.ncbi.nlm.nih.gov/pubmed/30534124 http://dx.doi.org/10.3389/fimmu.2018.02717 |
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