Hfe deficiency impairs pulmonary neutrophil recruitment in response to inflammation

Regulation of iron homeostasis and the inflammatory response are tightly linked to protect the host from infection. Here we investigate how imbalanced systemic iron homeostasis in a murine disease model of hereditary hemochromatosis (Hfe−/− mice) affects the inflammatory responses of the lung. We in...

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Hauptverfasser: Gente, Karolina (VerfasserIn) , Spasić Vujić, Maja (VerfasserIn) , Schäfer, Sebastian Markus (VerfasserIn) , Stolte, Jens (VerfasserIn) , Baehr-Ivacevic, Tomi (VerfasserIn) , Waldow, Katharina (VerfasserIn) , Zhou-Suckow, Zhe (VerfasserIn) , Klingmüller, Ursula (VerfasserIn) , Benes, Vladimir (VerfasserIn) , Mall, Marcus A. (VerfasserIn) , Muckenthaler, Martina (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: June 21, 2012
In: PLOS ONE
Year: 2012, Jahrgang: 7, Heft: 6
ISSN:1932-6203
DOI:10.1371/journal.pone.0039363
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1371/journal.pone.0039363
Verlag, kostenfrei, Volltext: http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0039363
Volltext
Verfasserangaben:Karolina Benesova, Maja Vujić Spasić, Sebastian M. Schaefer, Jens Stolte, Tomi Baehr-Ivacevic, Katharina Waldow, Zhe Zhou, Ursula Klingmueller, Vladimir Benes, Marcus A. Mall, Martina U. Muckenthaler
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Zusammenfassung:Regulation of iron homeostasis and the inflammatory response are tightly linked to protect the host from infection. Here we investigate how imbalanced systemic iron homeostasis in a murine disease model of hereditary hemochromatosis (Hfe−/− mice) affects the inflammatory responses of the lung. We induced acute pulmonary inflammation in Hfe−/− and wild-type mice by intratracheal instillation of 20 µg of lipopolysaccharide (LPS) and analyzed local and systemic inflammatory responses and iron-related parameters. We show that in Hfe−/− mice neutrophil recruitment to the bronchoalveolar space is attenuated compared to wild-type mice although circulating neutrophil numbers in the bloodstream were elevated to similar levels in Hfe−/− and wild-type mice. The underlying molecular mechanisms are likely multifactorial and include elevated systemic iron levels, alveolar macrophage iron deficiency and/or hitherto unexplored functions of Hfe in resident pulmonary cell types. As a consequence, pulmonary cytokine expression is out of balance and neutrophils fail to be recruited efficiently to the bronchoalveolar compartment, a process required to protect the host from infections. In conclusion, our findings suggest a novel role for Hfe and/or imbalanced iron homeostasis in the regulation of the inflammatory response in the lung and hereditary hemochromatosis.
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Beschreibung:Online Resource
ISSN:1932-6203
DOI:10.1371/journal.pone.0039363