Abstract
The innate immune system relies to a great deal on the interaction of pattern recognition receptors with pathogen- or damage-associated molecular pattern molecules. Extracellular histones belong to the latter group and their release has been described to contribute to the induction of systemic inflammatory reactions. However, little is known about their functions in the early immune response to an invading pathogen. Here we show that extracellular histones specifically target monocytes in human blood and this evokes the mobilization of the chemotactic chemokines CXCL9 and CXCL10 from these cells. The chemokine induction involves the toll-like receptor 4/myeloid differentiation factor 2 complex on monocytes, and is under the control of interferon-γ. Consequently, subcutaneous challenge with extracellular histones results in elevated levels of CXCL10 in a murine air pouch model and an influx of leukocytes to the site of injection in a TLR4 dependent manner. When analyzing tissue biopsies from patients with necrotizing fasciitis caused by Streptococcus pyogenes, extracellular histone H4 and CXCL10 are immunostained in necrotic, but not healthy tissue. Collectively, these results show for the first time that extracellular histones have an important function as chemoattractants as their local release triggers the recruitment of immune cells to the site of infection.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Chemokine CXCL10 / biosynthesis*
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Chemokine CXCL10 / immunology
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Chemokine CXCL9 / biosynthesis*
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Chemokine CXCL9 / immunology
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Chemokines / biosynthesis
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Chemotaxis, Leukocyte / immunology*
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Enzyme-Linked Immunosorbent Assay
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Female
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Histones / immunology*
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Humans
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Leukocytes / immunology*
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Leukocytes / metabolism
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Male
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Mice, Knockout
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Microscopy, Immunoelectron
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Monocytes / immunology
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Surface Plasmon Resonance
Substances
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Chemokine CXCL10
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Chemokine CXCL9
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Chemokines
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Histones
Grants and funding
This work was supported in part by the foundations of Alfred Österlund (
http://www.alfredosterlundsstiftelse.se), Crafoord (
http://www.crafoord.se), Greta and Johan Kock (
http://www.kockskastiftelsen.se), the Knut and Alice Wallenberg Foundation (
https://www.wallenberg.com/kaw/, KAW2011.0037), the Ragnar Söderberg Foundation (
http://ragnarsoderbergsstiftelse.se), Sten K Johnson Foundation (
http://www.stenkjohnsonsstiftelse.se), Sven-Olof Janson Lifework (
http://www.stiftelsen-sojansons-livsverk.se), the Royal Physiographic Society in Lund (
http://www.fysiografen.se/sv/), the Medical Faculty at Lund University (
http://www.med.lu.se), the Swedish Foundation for Strategic Research (
http://www.stratresearch.se, K2014-56X-13413-15-3) and the Swedish Research Council (
http://www.vr.se, SB12-0019). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.