journal article·2011-07-26Open access

Interactions between Magnetic Nanowires and Living Cells: Uptake, Toxicity, and Degradation

Malak Safi, Minhao Yan, Marie-Alice Guedeau-Boudeville, Hélène Conjeaud, Virginie Garnier-Thibaud, Nicole Boggetto, Armelle Baeza-Squiban, Florence Niedergang, Dietrich Averbeck, Jean-François Berret

ACS Nano· Volume 5· Issue 7

Abstract

We report on the uptake, toxicity, and degradation of magnetic nanowires by NIH/3T3 mouse fibroblasts. Magnetic nanowires of diameters 200 nm and lengths between 1 and 40 μm are fabricated by controlled assembly of iron oxide (γ-Fe(2)O(3)) nanoparticles. Using optical and electron microscopy, we show that after 24 h incubation the wires are internalized by the cells and located either in membrane-bound compartments or dispersed in the cytosol. Using fluorescence microscopy, the membrane-bound compartments were identified as late endosomal/lysosomal endosomes labeled with lysosomal associated membrane protein (Lamp1). Toxicity assays evaluating the mitochondrial activity, cell proliferation, and production of reactive oxygen species show that the wires do not display acute short-term (<100 h) toxicity toward the cells. Interestingly, the cells are able to degrade the wires and to transform them into smaller aggregates, even in short time periods (days). This degradation is likely to occur as a consequence of the internal structure of the wires, which is that of a noncovalently bound aggregate. We anticipate that this degradation should prevent long-term asbestos-like toxicity effects related to high aspect ratio morphologies and that these wires represent a promising class of nanomaterials for cell manipulation and microrheology.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoparticles: synthesis and applications · Cellular transport and secretion · Nanoparticle-Based Drug Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Matière et Systèmes Complexes, UMR 7057 CNRS Université Denis Diderot Paris-VII, Bâtiment Condorcet 10 rue Alice Domon et Léonie Duquet, 75205 Paris, France

Service de Microscopie Electronique, Institut de Biologie Intégrative, IFR 83 Université P. et M. Curie 9 quai St Bernard 75252 Paris cedex

Université Paris Diderot-Paris 7, ImagoSeine Bioimaging Core Facility, Jacques Monod Institute, 75013 Paris, France

Université Paris Diderot-Paris 7, Unit of Functional and Adaptive Biology (BFA) CNRS EAC 4413, Laboratory of Molecular and Cellular Responses to Xenobiotics, Bâtiment Buffon, 5 rue Thomas Mann, 75013 Paris, France

Inserm, U1016, Institut Cochin, Paris, France

CNRS, UMR 8104, Paris, France

Univ Paris Descartes, Paris, France

Institut Curie-Section de Recherche, Centre Universitaire Paris-Sud, Bâtiment 110 91405 Orsay, France

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