Munoz LE, Bilyy R, Biermann MHC, Kienhoefer D, Maueröder C, Hahn J, Brauner JM, Weidner D, Chen J, Scharin-Mehlmann M, Janko C, Friedrich RP, Mielenz D, Dumych T, Lootsik MD, Schauer C, Schett G, Hoffmann M, Zhao Y, Herrmann M (2016)
Publication Type: Journal article
Publication year: 2016
Book Volume: 113
Pages Range: E5856-E5865
Journal Issue: 40
The critical size for strong interaction of hydrophobic particles with phospholipid bilayers has been predicted to be 10 nm. Because of the wide spreading of nonpolar nanoparticles (NPs) in the environment, we aimed to reveal the ability of living organisms to entrap NPs via formation of neutrophil extracellular traps (NETs). Upon interaction with various cell types and tissues, 10- to 40-nm-sized NPs induce fast (<20 min) damage of plasma membranes and instability of the lysosomal compartment, leading to the immediate formation of NETs. In contrast, particles sized 100-1,000 nm behaved rather inertly. Resulting NET formation (NETosis) was accompanied by an inflammatory reaction intrinsically endowed with its own resolution, demonstrated in lungs and air pouches of mice. Persistence of small NPs in joints caused unremitting arthritis and bone remodeling. Small NPs coinjected with antigen exerted adjuvant-like activity. This report demonstrates a cellular mechanism that explains how small NPs activate the NETosis pathway and drive their entrapping and resolution of the initial inflammatory response.
APA:
Munoz, L.E., Bilyy, R., Biermann, M.H.C., Kienhoefer, D., Maueröder, C., Hahn, J.,... Herrmann, M. (2016). Nanoparticles size-dependently initiate self-limiting NETosis-driven inflammation. Proceedings of the National Academy of Sciences of the United States of America, 113(40), E5856-E5865. https://doi.org/10.1073/pnas.1602230113
MLA:
Munoz, Luis E., et al. "Nanoparticles size-dependently initiate self-limiting NETosis-driven inflammation." Proceedings of the National Academy of Sciences of the United States of America 113.40 (2016): E5856-E5865.
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