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Endothelial IL-33 Expression Is Augmented by Adenoviral Activation of the DNA Damage Machinery.

作者信息

Stav-Noraas Tor Espen, Edelmann Reidunn J, Poulsen Lars La Cour, Sundnes Olav, Phung Danh, Küchler Axel M, Müller Fredrik, Kamen Amine A, Haraldsen Guttorm, Kaarbø Mari, Hol Johanna

机构信息

K.G. Jebsen Inflammation Research Centre, Oslo University Hospital and University of Oslo, N-0424 Oslo, Norway.

Laboratory of Immunohistochemistry and Immunopathology, Department of Pathology, Oslo University Hospital and University of Oslo, N-0424 Oslo, Norway.

出版信息

J Immunol. 2017 Apr 15;198(8):3318-3325. doi: 10.4049/jimmunol.1600054. Epub 2017 Mar 3.

Abstract

IL-33, required for viral clearance by cytotoxic T cells, is generally expressed in vascular endothelial cells in healthy human tissues. We discovered that endothelial IL-33 expression was stimulated as a response to adenoviral transduction. This response was dependent on MRE11, a sensor of DNA damage that can also be activated by adenoviral DNA, and on IRF1, a transcriptional regulator of cellular responses to viral invasion and DNA damage. Accordingly, we observed that endothelial cells responded to adenoviral DNA by phosphorylation of ATM and CHK2 and that depletion or inhibition of MRE11, but not depletion of ATM, abrogated IL-33 stimulation. In conclusion, we show that adenoviral transduction stimulates IL-33 expression in endothelial cells in a manner that is dependent on the DNA-binding protein MRE11 and the antiviral factor IRF1 but not on downstream DNA damage response signaling.

摘要

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