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IL-1α is a DNA damage sensor linking genetoxic stress signaling to sterile inflammation and innate immunity

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Cohen,  Idan
Spemann Laboratory, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Tudor,  Cicerone
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Freudenberg,  Marina
Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Mittler,  G.
Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Citation

Cohen, I., Rider, P., Vornov, E., Tomas, M., Tudor, C., Wegner, M., et al. (2015). IL-1α is a DNA damage sensor linking genetoxic stress signaling to sterile inflammation and innate immunity. Scientific Reports, 5, 1-11.


Cite as: https://hdl.handle.net/someHandle/test/escidoc:902499
Abstract
Environmental signals can be translated into chromatin changes, which alter gene expression. Here we report a novel concept that cells can signal chromatin damage from the nucleus back to the surrounding tissue through the cytokine interleukin-1alpha (IL-1α). Thus, in addition to its role as a danger signal, which occurs when the cytokine is passively released by cell necrosis, IL-1α could directly sense DNA damage and act as signal for genotoxic stress without loss of cell integrity. Here we demonstrate localization of the cytokine to DNA-damage sites and its subsequent secretion. Interestingly, its nucleo-cytosolic shuttling after DNA damage sensing is regulated by histone deacetylases (HDAC) and IL-1α acetylation. To demonstrate the physiological significance of this newly discovered mechanism, we used IL-1α knockout mice and show that IL-1α signaling after UV skin irradiation and DNA damage is important for triggering a sterile inflammatory cascade in vivo that contributes to efficient tissue repair and wound healing.