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Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis

Variability in bacterial sterilization is a key feature of Mycobacterium tuberculosis (Mtb) disease. In a population of human macrophages, there are macrophages that restrict Mtb growth and those that do not. However, the sources of heterogeneity in macrophage state during Mtb infection are poorly u...

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Autores principales: Bryson, Bryan D., Rosebrock, Tracy R., Tafesse, Fikadu G., Itoh, Christopher Y., Nibasumba, Armel, Babunovic, Gregory H., Corleis, Bjorn, Martin, Constance, Keegan, Caroline, Andrade, Priscila, Realegeno, Susan, Kwon, Douglas, Modlin, Robert L., Fortune, Sarah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536549/
https://www.ncbi.nlm.nih.gov/pubmed/31133636
http://dx.doi.org/10.1038/s41467-019-10065-8
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author Bryson, Bryan D.
Rosebrock, Tracy R.
Tafesse, Fikadu G.
Itoh, Christopher Y.
Nibasumba, Armel
Babunovic, Gregory H.
Corleis, Bjorn
Martin, Constance
Keegan, Caroline
Andrade, Priscila
Realegeno, Susan
Kwon, Douglas
Modlin, Robert L.
Fortune, Sarah M.
author_facet Bryson, Bryan D.
Rosebrock, Tracy R.
Tafesse, Fikadu G.
Itoh, Christopher Y.
Nibasumba, Armel
Babunovic, Gregory H.
Corleis, Bjorn
Martin, Constance
Keegan, Caroline
Andrade, Priscila
Realegeno, Susan
Kwon, Douglas
Modlin, Robert L.
Fortune, Sarah M.
author_sort Bryson, Bryan D.
collection PubMed
description Variability in bacterial sterilization is a key feature of Mycobacterium tuberculosis (Mtb) disease. In a population of human macrophages, there are macrophages that restrict Mtb growth and those that do not. However, the sources of heterogeneity in macrophage state during Mtb infection are poorly understood. Here, we perform RNAseq on restrictive and permissive macrophages and reveal that the expression of genes involved in GM-CSF signaling discriminates between the two subpopulations. We demonstrate that blocking GM-CSF makes macrophages more permissive of Mtb growth while addition of GM-CSF increases bacterial control. In parallel, we find that the loss of bacterial control that occurs in HIV-Mtb coinfected macrophages correlates with reduced GM-CSF secretion. Treatment of coinfected cells with GM-CSF restores bacterial control. Thus, we leverage the natural variation in macrophage control of Mtb to identify a critical cytokine response for regulating Mtb survival and identify components of the antimicrobial response induced by GM-CSF.
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spelling pubmed-65365492019-05-29 Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis Bryson, Bryan D. Rosebrock, Tracy R. Tafesse, Fikadu G. Itoh, Christopher Y. Nibasumba, Armel Babunovic, Gregory H. Corleis, Bjorn Martin, Constance Keegan, Caroline Andrade, Priscila Realegeno, Susan Kwon, Douglas Modlin, Robert L. Fortune, Sarah M. Nat Commun Article Variability in bacterial sterilization is a key feature of Mycobacterium tuberculosis (Mtb) disease. In a population of human macrophages, there are macrophages that restrict Mtb growth and those that do not. However, the sources of heterogeneity in macrophage state during Mtb infection are poorly understood. Here, we perform RNAseq on restrictive and permissive macrophages and reveal that the expression of genes involved in GM-CSF signaling discriminates between the two subpopulations. We demonstrate that blocking GM-CSF makes macrophages more permissive of Mtb growth while addition of GM-CSF increases bacterial control. In parallel, we find that the loss of bacterial control that occurs in HIV-Mtb coinfected macrophages correlates with reduced GM-CSF secretion. Treatment of coinfected cells with GM-CSF restores bacterial control. Thus, we leverage the natural variation in macrophage control of Mtb to identify a critical cytokine response for regulating Mtb survival and identify components of the antimicrobial response induced by GM-CSF. Nature Publishing Group UK 2019-05-27 /pmc/articles/PMC6536549/ /pubmed/31133636 http://dx.doi.org/10.1038/s41467-019-10065-8 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bryson, Bryan D.
Rosebrock, Tracy R.
Tafesse, Fikadu G.
Itoh, Christopher Y.
Nibasumba, Armel
Babunovic, Gregory H.
Corleis, Bjorn
Martin, Constance
Keegan, Caroline
Andrade, Priscila
Realegeno, Susan
Kwon, Douglas
Modlin, Robert L.
Fortune, Sarah M.
Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title_full Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title_fullStr Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title_full_unstemmed Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title_short Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis
title_sort heterogeneous gm-csf signaling in macrophages is associated with control of mycobacterium tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536549/
https://www.ncbi.nlm.nih.gov/pubmed/31133636
http://dx.doi.org/10.1038/s41467-019-10065-8
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