Inflammation induces pro-NETotic neutrophils via TNFR2 signaling

Neuenfeldt F, Schumacher JC, Grieshaber-Bouyer R, Habicht J, Schröder-Braunstein J, Gauss A, Merle U, Niesler B, Heineken N, Dalpke A, Gaida MM, Giese T, Meuer S, Samstag Y, Wabnitz G (2022)


Publication Type: Journal article

Publication year: 2022

Journal

Book Volume: 39

Article Number: 110710

Journal Issue: 3

DOI: 10.1016/j.celrep.2022.110710

Abstract

Cytokines released during chronic inflammatory diseases induce pro-inflammatory properties in polymorphonuclear neutrophils (PMNs). Here, we describe the development of a subgroup of human PMNs expressing CCR5, termed CCR5+ PMNs. Auto- and paracrine tumor necrosis factor (TNF) signaling increases intracellular neutrophil elastase (ELANE) abundance and induces neutrophil extracellular traps formation (NETosis) in CCR5+ PMNs, and triggering of CCR5 amplifies NETosis. Membranous TNF (mTNF) outside-in signaling induces the formation of reactive oxygen species, known activators of NETosis. In vivo, we find an increased number of CCR5+ PMNs in the peripheral blood and inflamed lamina propria of patients with ulcerative colitis (UC). Notably, failure of anti-TNF therapy is associated with higher frequencies of CCR5+ PMNs. In conclusion, we identify a phenotype of pro-NETotic, CCR5+ PMNs present in inflamed tissue in vivo and inducible in vitro. These cells may reflect an important component of tissue damage during chronic inflammation and could be of diagnostic value.

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APA:

Neuenfeldt, F., Schumacher, J.C., Grieshaber-Bouyer, R., Habicht, J., Schröder-Braunstein, J., Gauss, A.,... Wabnitz, G. (2022). Inflammation induces pro-NETotic neutrophils via TNFR2 signaling. Cell Reports, 39(3). https://doi.org/10.1016/j.celrep.2022.110710

MLA:

Neuenfeldt, Friederike, et al. "Inflammation induces pro-NETotic neutrophils via TNFR2 signaling." Cell Reports 39.3 (2022).

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