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Home » Cellular uptake, as evaluated by TEM and NanoSIMS revealed that NPs internalization led to the formation of autophagosomes

Cellular uptake, as evaluated by TEM and NanoSIMS revealed that NPs internalization led to the formation of autophagosomes

Cellular uptake, as evaluated by TEM and NanoSIMS revealed that NPs internalization led to the formation of autophagosomes. proteins, and gene expression of LC3II, p62, NBR1, beclin1 and ATG5 by RT-qPCR. We also confirmed the formation and accumulation of autophagosomes in NPs treated cells with LC3-II upregulation. Based on the lack of degradation of p62 and NBR1 proteins, autophagosomes accumulation at a high dose (25.0?g/ml) is due to blockage while a low dose (0.16?g/ml) promoted autophagy. Cellular viability was not affected in either case. Conclusions The uptake of TiO2-NPs led to a dose-dependent increase in autophagic effect under non-cytotoxic conditions. Our results suggest dose-dependent autophagic effect over time as a cellular response to TiO2-NPs. Most importantly, these findings suggest that simple toxicity data are Slit3 not enough to understand the full impact of TiO2-NPs and their effects on cellular pathways or function. [19]. However, a study by Shi et al. provides evidence that TiO2-NPs (5C20?nm) can penetrate the skin and interact with the immune system [15]. In addition, the presence of 14?nm silica coated TiO2-NPs within the epidermis and superficial dermis has been observed [20]. Therefore, our goal was to use in vitro keratinocytes (HaCaT) to investigate the interactions of TiO2-NPs with cellular autophagy at non-cytotoxic doses. We used then uncoated TiO2-NPs (18?nm) to investigate the impact on cytotoxicity, ROS generation and uptake behavior under acute treatment to define the non-cytotoxic levels. Here we statement that TiO2-NPs dose may shift the effects on autophagy from induction to blockage. These findings may open up the possibility of modulating autophagy by NPs through tuning their dose. Results NPs characterization Characterization of TiO2-NPs was carried out by transmission electron microscopy (TEM), zeta potential (Z-potential) measurement and dynamic light scattering (DLS) in water and cell culture medium (Fig.?1 and Table?1). TEM images of TiO2-NPs exhibited a near-spherical shape and aggregates. The hydrodynamic sizes and zeta potentials of TiO2-NPs in both water and in cell culture media showed that TiO2-NPs suspensions were unstable and aggregating. Open in a separate windows Fig.?1 Characterization of TiO2-NPs in cell culture medium. a Representative TEM image of 18?nm TiO2-NPs in DMEM medium. b Dynamic light scattering analysis with TiO2-NPs suspended in DMEM cell culture medium. Analyses were performed from your stock answer (1?mg/mL). (for aCb images are 10?m and for cCf images are 2?m. nucleus Open in a separate window Fig.?5 NanoSIMS confirms TiO2-NPs are uptake and are not inside nucleus. NanoSIMS images of the elemental distribution of 12C14N and 48Ti16O on an ultra-section cut of HaCaT cells exposed to TiO2-NPs at a low dose (0.16?g/mL)low dose and b high-dose (25.0?g/mL)high dose for 24?h. Acquisition time 30?ms/pixel. represent 5?m To improve the resolution of the characterization of the TiO2-NPs uptake, we combined TEM observations with NanoSIMS analysis (Fig.?5) [25]. NanoSIMS analysis confirmed that this aggregates/agglomerates were composed of TiO2-NPs and revealed their localization (Fig.?5). We found presence of TiO2-NPs in the cytoplasm, while no traces of titanium were detected in the nucleus. The NPs accumulated around the nuclear membrane without diffusion into the nucleus. The micrometric size of the titanium signals as observed in NanoSIMS50 figures indicated that this NPs were agglomerated (Fig.?5a, b). TiO2-NPs trigger an autophagic response by increasing LC3 translocation Treated cells exhibited a distinctive mark of autophagy, autophagosomes formation (Fig.?6). We monitored LC3 protein conversion by using HaCaT cells Brompheniramine transiently transfected with an eGFP-LC3 expressing plasmid. GFP-LC3 punctates were assessed at 1 and 24?h in eGFP-LC3 expressing cells incubated with low- and high-dose of TiO2-NPs and the relative quantity of fluorescent puncta formed per cell was quantified (Fig.?6a, b). The cytoplasmic LC3 (LC3I) inactive appears diffused throughout the Brompheniramine cytoplasm, while activated LC3 (LC3II) appear as bright punctates (Fig.?6a). Quantification of eGFP-LC3 dots showed a significant increase after 1 and 24?h exposure to high-dose of NPs compared with untreated cells. There were equivalent Brompheniramine numbers of puncta per cell for high- and low-doses at.

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