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Date publication

février 2026

Journal

NanoImpact

Auteurs

Membres identifiés du Cancéropôle Est :
Dr CIANFERANI Sarah


Tous les auteurs :
Collin-Faure V, Villacorta A, Diemer H, Cianférani S, Marcos R, Hernandez A, Carrière M, Darrouzet E, Rabilloud T

Résumé

Micro and nanoplastics are pollutants which concentration in different biotopes increases continuously over time, which poses the question of their potential effects on health. In animals, these micro and nanoplastics are recognized as particulate materials and thus handled by macrophages,which are therefore a key cell type to study. Most studies have used an experimental scheme in which the cells of interest are exposed to a single dose of plastics, and where the readout of the studied parameters is made immediately after exposure. However, this classical experimental scheme does not take into account the impact of biopersistence, nor the potential cellular adaptation that may take place when cells are exposed repeatedly to a low dose of plastics. We thus used a repeated exposure scheme, in order to better take into account these phenomena. Within this frame, we compared the macrophages responses to a persistent nanoplastic, i.e. true-to-life polyethylene terephthalate nanoparticles and to a biodegradable nanoplastic, i.e. polycaprolactone, by a combination of proteomic and targeted experiments. Our results show that under this repeated exposure scheme, the proteome changes were of a lesser extent than under the acute exposure mode, indicating cell adaptation. However, polyethylene terephthalate nanoparticles induced oxidative stress, a slight depression of phagocytosis and a pro-inflammatory response, while polycaprolactone nanoparticles induced a depression of macrophages functions, especially regarding cytokines production (Interleukin 6, MCP-1, TNF alpha) in response to a bacterial challenge (represented by a lipopolysaccharide challenge), indicating harmful but different effects of both nanoplastics even in the repeated exposure scheme.

Mots clés

Immune response, Inflammation, Macrophages, Nanoplastics, Oxidative stress, Poly (ethylene terephthalate), Polycaprolactone

Référence

NanoImpact. 2026 02 21;:100615