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Collective nitric oxide production provides tissue-wide immunity during Leishmania infection
Romain Olekhnovitch, … , Andreas J. Müller, Philippe Bousso
Romain Olekhnovitch, … , Andreas J. Müller, Philippe Bousso
Published March 10, 2014
Citation Information: J Clin Invest. 2014;124(4):1711-1722. https://doi.org/10.1172/JCI72058.
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Research Article Microbiology

Collective nitric oxide production provides tissue-wide immunity during Leishmania infection

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Abstract

Nitric oxide (NO) production is critical for the host defense against intracellular pathogens; however, it is unclear whether NO-dependent control of intracellular organisms depends on cell-intrinsic or cell-extrinsic activity of NO. For example, NO production by infected phagocytes may enable these cells to individually control their pathogen burden. Alternatively, the ability of NO to diffuse across cell membranes might be critical for infection control. Here, using a murine ear infection model, we found that, during infection with the intracellular parasite Leishmania major, expression of inducible NO synthase does not confer a cell-intrinsic ability to lower parasite content. We demonstrated that the diffusion of NO promotes equally effective parasite killing in NO-producing and bystander cells. Importantly, the collective production of NO by numerous phagocytes was necessary to reach an effective antimicrobial activity. We propose that, in contrast to a cell-autonomous mode of pathogen control, this cooperative mechanism generates an antimicrobial milieu that provides the basis for pathogen containment at the tissue level.

Authors

Romain Olekhnovitch, Bernhard Ryffel, Andreas J. Müller, Philippe Bousso

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Figure 1

Tracking the fate of recruited phagocytes at the site of infection.

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Tracking the fate of recruited phagocytes at the site of infection.
(A) ...
(A) C57BL/6 mice were infected with DsRed-expressing L. major parasites in the ear dermis. Two weeks later, infected ear tissues were stained for intracellular iNOS and analyzed by flow cytometry. (B) Experimental set up of BMC transfers. GFP-expressing BMCs were transferred to recipients after 2 weeks of infection. Infected ear tissues were analyzed from day 1 to day 5 after injection by flow cytometry. (C) Representative flow cytometry plots of infected ear tissues harvested either 2 or 3 days after BMC injection. (D) Plots correspond to cell population frequencies measured by flow cytometry. Green, blue, and pink shading in C and D identify Ly6C+ MHC class II–, Ly6C+ MHC II+, and Ly6C– MHC II+ cell populations, respectively. Each dot represents an individual ear; horizontal lines represent average values. Numbers shown in flow cytometry profiles represent the percentage of cells falling into the indicated region.*P < 0.05; **P < 0.01; ***P < 0.001. Data are representative of 2 independent experiments.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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