Dynamic neutrophil lipidome remodeling during induction of NETosis

Neutrophil extracellular trap formation (NETosis) affects a wide variety of clinically relevant human diseases. Although lipid remodeling is essential for neutrophil function and membrane rupture during NETosis, the neutrophil lipidome and its dynamics have not been characterized. Thus, we establish a quantitative lipidome of human neutrophils comprising 1048 species across nine orders of magnitude and map its remodeling during NETosis. NET formation caused profound alterations in the phosphatidylinositol, phosphatidic acid, diacylglycerol (DG), and lyso-glycerophospholipid levels. Calcium- and reactive oxygen species-dependent NETosis pathways displayed distinct lipidomic trajectories yet converged on the significance of phospholipid lipase networks. Pharmacological inhibition of this networks altered lipid composition and markedly impaired NETosis, while DG treatment revoked the effect. Together, our findings reveal lipid remodeling as a fundamental determinant of NETosis and identify interconnected and dependent phospholipid lipase networks with downstream DG-dependent signaling as a potential therapeutic target in NET-associated diseases.

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Publication Details

Journal
Science Advances
Published
2026-06-24
DOI
https://doi.org/10.1126/sciadv.aec9891
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Dynamic neutrophil lipidome remodeling during induction of NETosis

Jann Arden, Stefanie Rubenzucker, Jesse A. Michael, Patrick Münzer et al.
Science Advances
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

Dynamic neutrophil lipidome remodeling during induction of NETosis

Jann Arden, Stefanie Rubenzucker, Jesse A. Michael, Patrick Münzer, Reuben S. E. Young, Cristina Coman, Melina Fischer, Oliver Borst, Robert Ahrends, Shane R. Ellis, Nina Troppmair, Jens Martin, Ferdinand Kollotzek, Monika Zdanytė, Claudia Hornef, Gundula D. Lingens, Nils Sülzle
article en

Abstract

Neutrophil extracellular trap formation (NETosis) affects a wide variety of clinically relevant human diseases. Although lipid remodeling is essential for neutrophil function and membrane rupture during NETosis, the neutrophil lipidome and its dynamics have not been characterized. Thus, we establish a quantitative lipidome of human neutrophils comprising 1048 species across nine orders of magnitude and map its remodeling during NETosis. NET formation caused profound alterations in the phosphatidylinositol, phosphatidic acid, diacylglycerol (DG), and lyso-glycerophospholipid levels. Calcium- and reactive oxygen species-dependent NETosis pathways displayed distinct lipidomic trajectories yet converged on the significance of phospholipid lipase networks. Pharmacological inhibition of this networks altered lipid composition and markedly impaired NETosis, while DG treatment revoked the effect. Together, our findings reveal lipid remodeling as a fundamental determinant of NETosis and identify interconnected and dependent phospholipid lipase networks with downstream DG-dependent signaling as a potential therapeutic target in NET-associated diseases.

Science AdvancesVol. 12(26)
University of Vienna (AT), University of Wollongong (AU), Thrombosis Research Institute (GB), University of Tübingen (DE)
Deutsche Forschungsgemeinschaft, Austrian Science Fund, Universität Wien
Openalex Percentile: Top 10%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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