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

Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Bryson, Bryan D.;
Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Rosebrock, Tracy R.;
Zugehörigkeit
Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, United States
Tafesse, Fikadu G.;
Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Itoh, Christopher Y.;
Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Nibasumba, Armel;
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Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Babunovic, Gregory H.;
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1223547914
Zugehörigkeit
Ragon Institute of MGH, MIT, and Harvard, 400 Technology Square Cambridge, Cambridge, United States
Corleis, Björn;
Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Martin, Constance;
Zugehörigkeit
Division of Dermatology, David Geffen School of Medicine at University of California, United States
Keegan, Caroline;
Zugehörigkeit
Division of Dermatology, David Geffen School of Medicine at University of California, United States
Andrade, Priscila;
Zugehörigkeit
Division of Dermatology, David Geffen School of Medicine at University of California, United States
Realegeno, Susan;
Zugehörigkeit
Ragon Institute of MGH, MIT, and Harvard, 400 Technology Square Cambridge, Cambridge, United States
Kwon, Douglas;
Zugehörigkeit
Division of Dermatology, David Geffen School of Medicine at University of California, United States
Modlin, Robert L.;
Zugehörigkeit
Harvard T. H. Chan School of Public Health, 655 Huntington Avenue Boston, Boston, United States
Fortune, Sarah M.

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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