2014
DOI: 10.1016/j.nano.2014.02.001
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Toxicity of carboxylated carbon nanotubes in endothelial cells is attenuated by stimulation of the autophagic flux with the release of nanomaterial in autophagic vesicles

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Cited by 63 publications
(38 citation statements)
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“…Lysosomes also play an important role in the degradation of engulfed particles, and nanoparticle exposure may impair the fusion of autophagosomes with lysosomes (Stern et al, 2012). A recent study showed that carbon nanotube exposure induced autophagosome accumulation due to a blockade of the autophagic flux, whereas pharmacological stimulation of the autophagic flux promoted extracellular efflux of nanoparticles and attenuated nanoparticle-induced toxicity (Orecna et al, 2014). Thus, it is possible that the altered lysosomal activity may impair digestion and efflux of particles and lipids, which may be the mechanisms of A-DEP induced lipid droplet formation in macrophages.…”
Section: Discussionmentioning
confidence: 99%
“…Lysosomes also play an important role in the degradation of engulfed particles, and nanoparticle exposure may impair the fusion of autophagosomes with lysosomes (Stern et al, 2012). A recent study showed that carbon nanotube exposure induced autophagosome accumulation due to a blockade of the autophagic flux, whereas pharmacological stimulation of the autophagic flux promoted extracellular efflux of nanoparticles and attenuated nanoparticle-induced toxicity (Orecna et al, 2014). Thus, it is possible that the altered lysosomal activity may impair digestion and efflux of particles and lipids, which may be the mechanisms of A-DEP induced lipid droplet formation in macrophages.…”
Section: Discussionmentioning
confidence: 99%
“…This effect is partly attenuated upon mild stimulation of autophagy using low doses of bafilomycin A1, which causes extracellular release of nanomaterial from autophagic vesicles [57]. Exocytosis of autophagic vesicles has been proposed as a mechanism of release of nanomaterials.…”
Section: Blockage Of Autophagic Fluxmentioning
confidence: 99%
“…One method reported by several groups is to sonicate cCNT soot in deionized water before adding the resulting aqueous cCNT suspension to cell culture medium,[1014] while others have reported an additional centrifugation step to purify the aqueous cCNT suspension (herewith called a centrifuged cCNT suspension) before adding this material to cell culture medium or blood. [1518] Another important consideration for biomedical applications of CNTs is therefore a thorough physiochemical characterization of the exact CNT sample that is presented to living cells or intact organisms. [1928] At a minimum, this involves some measure of CNT structures, amounts, dimensions, porosities, impurities, and in the case of cCNTs, a measure of surface acidity, defined as the acidic groups covalently attached to cCNT surfaces and potential acidic carbonaceous substances adsorbed to cCNT surfaces (i.e., oxidative debris).…”
Section: Introductionmentioning
confidence: 99%