Litcius/Paper detail

NETosis proceeds by cytoskeleton and endomembrane disassembly and PAD4-mediated chromatin decondensation and nuclear envelope rupture

Hawa Racine Thiam, Siu Ling Wong, Rong Qiu, Mark Kittisopikul, Amir Vahabikashi, Anne E. Goldman, Robert D. Goldman, Denisa D. Wagner, Clare M. Waterman

2020Proceedings of the National Academy of Sciences412 citationsDOIOpen Access PDF

Abstract

to induce NETosis. Upon stimulation, cells exhibited rapid disassembly of the actin cytoskeleton, followed by shedding of plasma membrane microvesicles, disassembly and remodeling of the microtubule and vimentin cytoskeletons, ER vesiculation, chromatin decondensation and nuclear rounding, progressive plasma membrane and nuclear envelope (NE) permeabilization, nuclear lamin meshwork and then NE rupture to release DNA into the cytoplasm, and finally plasma membrane rupture and discharge of extracellular DNA. Inhibition of actin disassembly blocked NET release. Mouse and dHL-60 cells bearing genetic alteration of PAD4 showed that chromatin decondensation, lamin meshwork and NE rupture and extracellular DNA release required the enzymatic and nuclear localization activities of PAD4. Thus, NETosis proceeds by a stepwise sequence of cellular events culminating in the PAD4-mediated expulsion of DNA.

Topics & Concepts

Cell biologyNeutrophil extracellular trapsCytoskeletonChromatinEndomembrane systemBiologyInflammationInnate immune systemProgrammed cell deathDNA damageImmune systemCellDNAImmunologyApoptosisGeneticsGolgi apparatusEndoplasmic reticulumNeutrophil, Myeloperoxidase and Oxidative MechanismsCell Adhesion Molecules ResearchVasculitis and related conditions