Polystyrene Nanoparticles Research Articles

Ecotoxicity of emerging contaminants in the reproductive organ of marine mussels Mytilus galloprovincialis

Contaminants of emerging concern (CECs) present a new threat to the marine environment, and it is vital to understand the interactions and possible toxicity of CEC mixtures once they reach the ocean. CECs—such as metal nanoparticles, nanoplastics, and pharmaceuticals—are groups of contaminants some of which have been individually evaluated, though their interactions as mixtures are still not fully understood. To ensure a healthy and prosperous future generation, successful reproduction is key: however, if hindered, population dynamics may be at danger leading to a negative impact on biodiversity. This study aimed to understand the effects of silver (20 nm nAg, 10 μg/L), polystyrene nanoparticles (50 nm nPS, 10 μg/L), and 5-fluorouracil (5FU, 10 ng/L) individually and as a mixture (10 μg/L of nPS + 10 μg/L of nAg +10 ng/L of 5FU) in the gonads of Mytilus galloprovincialis. A multibiomarker approach, namely the antioxidant defence system (ADS; superoxide dismutase, catalase, glutathione peroxidases, glutathione – S – transferases activities), and oxidative damage (OD; lipid peroxidation) were analysed in the gonads of mussels. All exposure treatments after 3 days led to an increase of enzymatic activity, followed by an inhibition after 14 and 21 days. Thus, ADS was overwhelmed due to the generation of ROS, resulting in OD, except for nPS exposed mussels. The OD in Mix exposed mussels increased exponentially by 57-fold. When CEC mixtures interact, they are potentially more hazardous than their individual components, posing a major threat to marine species. To understand synergistic and antagonistic interactions, a model was applied, and antagonistic interactions were observed in evaluated biomarkers at all time-points, apart from a synergistic interaction at day 3 relative to LPO. Results indicate that the effects observed in Mix-exposed mussel gonads are mainly due to the interaction of nAg and 5FU but not nPS.

Creating optical centrifuge for particle clearing and separation

Optical centrifuge has recently experienced growing attention as a promising tool for optically manipulating various small particles in different applications such as particle clearing and separation. Herein, we report a novel optical centrifuge, which is driven by optical force arising from transverse phase gradient of light. The particle clearing and separation have been experimentally demonstrated as application examples, by using Au and polystyrene nanoparticles. The experimental results show that the optical centrifuge exhibits high performance while used for optically clearing and separating nanoparticles. For instance, its centrifuge velocity in optical clearing can reach its peak speed of 120 μm/s in a short time, which is highly desirable for optical manipulation of various particles in microfluidic systems. Importantly, it has remarkable advantages, including high speed, flexible design and ease of control, which offers a new way for versatile optical manipulation of particles in microfluidic systems.

Generation of polystyrene-specific antibodies for developing immunoassays to analyze microplastics and nanoplastics

Micro- and nano-plastics (MNPs) are emerging pollutants that have drawn worldwide attention due to their negative impacts on the health and sustainability of our ecosystem. Quantitative analysis of MNPs, especially those at nano-scale, is still challenging due to lack of efficient analytical methods. Different antibody-based immunoassay platforms have been well established and readily available for rapid, specific, and quantitative analysis of targets with a broad size range. The key to developing immunoassays for MNP analysis is to generate plastic-specific antibodies, which is still lacking. In this study, we conjugated the nanoparticles of polystyrene (PS), a widely studied representative MNPs, to different carrier proteins for rabbit immunizations. The PS-specific antibodies were significantly induced upon immunization (up to 128-fold increase in IgG titer), which was validated by multi-tier immunoassays using different PS products. Notably, the PS-specific antibodies did not react with polypropylene, a different plastic. Using PS antibody-based enzyme-linked immunoassay, we further demonstrated suitability of the antibody-based immunoassay for quantitative analysis of the PS particles that have been exposed to diverse matrices. Together, this study, for the first time, demonstrates the feasibility of producing plastic-specific antibodies, and lays the groundwork to develop innovative antibody-based immunoassays for future risk assessment and management of MNPs, particularly those at nano-scale.

Accurate Sizing of Nanoparticles Using a High-Throughput Charge Detection Mass Spectrometer without Energy Selection.

The sizes and shapes of nanoparticles play a critical role in their chemical and material properties. Common sizing methods based on light scattering or mobility lack individual particle specificity, and microscopy-based methods often require cumbersome sample preparation and image analysis. A promising alternative method for the rapid and accurate characterization of nanoparticle size is charge detection mass spectrometry (CDMS), an emerging technique that measures the masses of individual ions. A recently constructed CDMS instrument designed specifically for high acquisition speed, efficiency, and accuracy is described. This instrument does not rely on an ion energy filter or estimates of ion energy that have been previously required for mass determination, but instead uses direct, in situ measurements. A standardized sample of ∼100 nm diameter polystyrene nanoparticles and ∼50 nm polystyrene nanoparticles with amine-functionalized surfaces are characterized using CDMS and transmission electron microscopy (TEM). Individual nanoparticle masses measured by CDMS are transformed to diameters, and these size distributions are in close agreement with distributions measured by TEM. CDMS analysis also reveals dimerization of ∼100 nm nanoparticles in solution that cannot be determined by TEM due to the tendency of nanoparticles to agglomerate when dried onto a surface. Comparing the acquisition and analysis times of CDMS and TEM shows particle sizing rates up to ∼80× faster are possible using CDMS, even when samples ∼50× more dilute were used. The combination of both high-accuracy individual nanoparticle measurements and fast acquisition rates by CDMS represents an important advance in nanoparticle analysis capabilities.

Combinational exposure to hydroxyatrazine increases neurotoxicity of polystyrene nanoparticles on Caenorhabditis elegans

Using Caenorhabditis elegans as an animal model, we investigated combinational effect between 2-hydroxyatrazine (HA) and polystyrene nanoparticle (PS-NP) on function and development of D-type motor neurons. Exposure to HA (10 and 100 μg/L) alone caused decreases in body bend, head thrash, and forward turn and increase in backward turn. Exposure to 100 μg/L HA also caused neurodegeneration of D-type motor neurons. Moreover, combinational exposure to HA (0.1 and 1 μg/L) induced enhancement in PS-NP (10 μg/L) toxicity in inhibiting body bend, head thrash, and forward turn, and in increasing backward turn. In addition, combinational exposure to HA (1 μg/L) could result in neurodegeneration of D-type motor neurons in PS-NP (10 μg/L) exposed nematodes. Combinational exposure to HA (1 μg/L) and PS-NP (10 μg/L) increased expressions of crt-1, itr-1, mec-4, asp-3, and asp-4, which govern the induction of neurodegeneration. Moreover, combinational exposure to HA (0.1 and 1 μg/L) strengthened PS-NP (10 μg/L)-induced decreases in glb-10, mpk-1, jnk-1, and daf-7 expressions, which encode neuronal signals regulating response to PS-NP. Therefore, our results demonstrated the effect of combinational exposure to HA and nanoplastics at environmentally relevant concentrations in causing toxic effect on nervous system in organisms.

Untangling the Interactions between Anionic Polystyrene Nanoparticles and Lipid Membranes Using Laurdan Fluorescence Spectroscopy and Molecular Simulations.

Several classes of synthetic nanoparticles (NPs) induce rearrangements of cell membranes that can affect membrane function. This paper describes the investigation of the interactions between polystyrene nanoparticles and liposomes, which serve as model cell membranes, using a combination of laurdan fluorescence spectroscopy and coarse-grained molecular dynamics (MD) simulations. The relative intensities of the gel-like and fluid fluorescent peaks of laurdan, which is embedded in the liposome membranes, are quantified from the areas of deconvoluted lognormal laurdan fluorescence peaks. This provides significant advantages in understanding polymer-membrane interactions. Our study reveals that anionic polystyrene NPs, which are not cross-linked, induce significant membrane rearrangement compared to other cationic or anionic NPs. Coarse-grained MD simulations demonstrate that polymer chains from the anionic polystyrene NP penetrate the liposome membrane. The inner leaflet remains intact throughout this process, though both leaflets show a decrease in lipid packing that is indicative of significant local rearrangement of the liposome membrane. These results are attributed to the formation of a hybrid gel made up of a combination of polystyrene (PS) and lipids that forces water molecules away from laurdan. Our study concludes that a combination of negative surface charge to interact electrostatically with positive charges on the membrane, a hydrophobic core to provide a thermodynamic preference for membrane association, and the ability to extend non-cross linked polymer chains into the liposome membrane are necessary for NPs to cause a significant rearrangement in the liposomes.

Fabrication of superhydrophobic surfaces for applications in total internal reflection effects

Superhydrophobic surfaces have attracted significant attention in the applied science community. This paper presents three different methods for fabricating superhydrophobic surfaces, which can be applied in liquid light guides with the total internal reflection effect playing a central role. The selective bi-polymer etching only produces a hydrophobic porous poly(methyl methacrylate) surface but is simple and versatile for use on an arbitrary surface. In metal-assisted chemical etching, wet etching of a silver layer on a silicon sample creates porous silicon with superhydrophobicity, characterized by a water contact angle of 160°. The metal-assisted chemical etching method modified with the presence of polystyrene nanoparticles further improved the water contact angle to 164° by creating a nanopillar silicon structure. The metal-assisted chemical etching methods are more complicated but can produce superhydrophobic surfaces with very high water contact angles. These results show that superhydrophobic surfaces fabricated by methods in this study can be used for total internal reflection effect at the interface between water with huge potential applications in liquid light guides.

Fabrication of Partially Etched Polystyrene Nanoparticles.

Non-spherical polymer nanoparticles (NPs) have gained attention in various fields, but their fabrication remains challenging. In this study, we present a simple protocol for synthesizing partially etched polystyrene (PS) nanoparticles through emulsion polymerization and chemical etching. By adjusting the degree of crosslinking, we selectively dissolve the weakly crosslinked portions of the particles, resulting in partially etched PS NPs with increased surface area. These partially etched NPs are evaluated for their use as solid surfactants in Pickering emulsions, where they demonstrate significantly improved emulsion stability compared to intact spherical NPs. Our results contribute to the field of nanoparticle shape control and provide insights into developing novel materials for various applications, particularly in the area of solid surfactant usage. Additionally, the importance of conducting cellular toxicity studies using these partially etched NPs for future work is also emphasized.

The role of algal EPS in reducing the combined toxicity of BPA and polystyrene nanoparticles to the freshwater algae Scenedesmus obliquus

Both Bisphenol A (BPA) and polystyrene nanoplastics (PSNPs) are routinely found in several consumer products such as packaging materials, flame retardants, and cosmetics. The environment is seriously endangered by nano- and microplastics. In addition to harming aquatic life, nanoplastics (NPs) also bind to other pollutants, facilitating their dispersion in the environment and possibly promoting toxicity induced by these pollutants. The toxic effects of polystyrene nanoplastics (PS-NPs) and BPA were examined in this study, as well as the combined toxic impacts of these substances on the freshwater microalgae Scenedesmus obliquus. In addition, the exopolymeric substances (EPS) secreted by algae will interact with the pollutants modifying their physicochemical behaviour and fate. This work aimed to investigate how algal EPS alters the combined effects of BPA and PSNPs on the microalgae Scenedesmus obliquus. The algae were exposed to binary mixtures of BPA (2.5, 5, and 10 mg/L) and PSNPs (1 mg/L of plain, aminated, and carboxylated PSNPs) with EPS added to the natural freshwater medium. Cell viability, hydroxyl and superoxide radical generation, cell membrane permeability, antioxidant enzyme activity (catalase and superoxide dismutase), and photosynthetic pigment content were among the parameters studied to determine the toxicity. It was observed that for all the binary mixtures, the carboxylated PSNPs were most toxic when compared to the toxicity induced by the other PSNP particles investigated. The maximum damage was observed for the mixture of 10 mg/L of BPA with carboxylated PSNPs with a cell viability of 49%. When compared to the pristine mixtures, the EPS-containing mixtures induced significantly reduced toxic effects. A considerable decrease in reactive oxygen species levels, activity of antioxidant enzymes (SOD and CAT), and cell membrane damage was noted in the EPS-containing mixtures. Reduced concentrations of the reactive oxygen species led to improved photosynthetic pigment content in the cells.

Exposure to nanoplastics induces mitochondrial impairment and cytomembrane destruction in Leydig cells

Plastic particle pollution poses an emerging threat to ecological and human health. Laboratory animal studies have illustrated that nano-sized plastics can accumulate in the testis and cause testosterone deficiency and spermatogenic impairment. In this study, TM3 mouse Leydig cells were in vitro exposed to polystyrene nanoparticles (PS-NPs, size 20 nm) at dosages of 50, 100 and 150 μg/mL to investigate their cytotoxicity. Our results demonstrated that PS-NPs can be internalized into TM3 Leydig cells and led to a concentration-dependent decline in cell viability. Furthermore, PS-NPs stimulation amplified ROS generation and initiated cellular oxidative stress and apoptosis. Moreover, PS-NPs treatment affected the mitochondrial DNA copy number and collapsed the mitochondrial membrane potential, accompanied by a disrupted energy metabolism. The cells exposed to PS-NPs also displayed a down-regulated expression of steroidogenesis-related genes StAR, P450scc and 17β-HSD, along with a decrease in testosterone secretion. In addition, treatment with PS-NPs destructed plasma membrane integrity, as presented by increase in lactate dehydrogenase release and depolarization of cell membrane potential. In summary, these data indicated that exposure to PS-NPs in vitro produced cytotoxic effect on Leydig cells by inducing oxidative injury, mitochondrial impairment, apoptosis, and cytomembrane destruction. Our results provide new insights into male reproductive toxicity caused by NPs.

Kinetics of autophagic activity in nanoparticle-exposed lung adenocarcinoma (A549) cells.

Autophagy, a homeostatic mechanism, is crucial in maintaining normal cellular function. Although dysregulation of autophagic processes is recognized in certain diseases, it is unknown how maintenance of cellular homeostasis might be affected by the kinetics of autophagic activity in response to various stimuli. In this study, we assessed those kinetics in lung adenocarcinoma (A549) cells in response to exposure to nanoparticles (NP) and/or Rapamycin. Since NP are known to induce autophagy, we wished to determine if this phenomenon could be a driver of the harmful effects seen in lung tissues exposed to air pollution. A549 cells were loaded with a fluorescent marker (DAPRed) that labels autophagosomes and autolysosomes. Autophagic activity was assessed based on the fluorescence intensity of DAPRed measured over the entire cell volume of live single cells using confocal laser scanning microscopy (CLSM). Autophagic activity over time was determined during exposure of A549 cells to single agents (50 nM Rapamycin; 80 μg/mL, 20 nm carboxylated polystyrene NP (PNP); or, 1 μg/mL ambient ultrafine particles (UFP) (<180 nm)), or double agents (Rapamycin + PNP or Rapamycin + UFP; concomitant and sequential), known to stimulate autophagy. Autophagic activity increased in all experimental modalities, including both single agent and double agent exposures, and reached a steady state in all cases ~2 times control from ~8 to 24 hrs, suggesting the presence of an upper limit to autophagic capacity. These results are consistent with the hypothesis that environmental stressors might exert their harmful effects, at least in part, by limiting available autophagic response to additional stimulation, thereby making nanoparticle-exposed cells more susceptible to secondary injury due to autophagic overload.

Daphnia magna uptake and excretion of luminescence‐labelled polystyrene nanoparticle as visualized by high sensitivity real-time optical imaging

The environmental and ecological consequences of nanoplastics (NPs) draw increasing research interests and social concerns. However, the in situ and real‐time detection of NPs from living organisms and transferring media remains as a major technical obstacle for scientific investigation. Herein we report a novel time-gated imaging (TGI) strategy capable of real-time visualizing the intake of NPs by an individual living organism, which is based on the polystyrene NPs labelled with lanthanide up‐conversion luminescence. The limit of detection (LOD) of the TGI apparatus was 600 pg (SNR = 3) in a field of view of 2.4 × 3.8 mm. Taking Daphnia magna as the aquatic model, we investigated the dynamics of uptake and accumulation of NPs (500 μg/L) for 24 h, and the subsequent excretion process (in clean medium) for 48 h, and quantitively analyzed the distribution and the overall mass of NPs deposited in D. magna. The uptake of NPs via filter‐feeding occurred in a few minutes, whereas a longer accumulation was found, in a timescale of several hours. And similar behaviors (bi-phase elimination) were also seen in the excretion, indicating the migration of NPs into the circulatory system. The average mass of NPs accumulated in an individual D. magna was ∼12 ng after 24 h exposure, indicating that D. magna as a filter feeder tends to retain NPs. The observed NPs accumulation in D. magna exemplifies the potential risk of aquatic ecosystem on exposure to NP contamination.

Impact of Nanoparticle Physicochemical Properties on Protein Corona and Macrophage Polarization.

Macrophages, the major component of the mononuclear phagocyte system, uptake and clear systemically administered nanoparticles (NPs). Therefore, leveraging macrophages as a druggable target may be advantageous to enhance NP-mediated drug delivery. Despite many studies focused on NP-cell interactions, NP-mediated macrophage polarization mechanisms are still poorly understood. This work aimed to explore the effect of NP physicochemical parameters (size and charge) on macrophage polarization. Upon exposure to biological fluids, proteins rapidly adsorb to NPs and form protein coronas. To this end, we hypothesized that NP protein coronas govern NP-macrophage interactions, uptake, and subsequent macrophage polarization. To test this hypothesis, model polystyrene NPs with various charges and sizes, as well as NPs relevant to drug delivery, were utilized. Data suggest that cationic NPs potentiate both M1 and M2 macrophage markers, while anionic NPs promote M1-to-M2 polarization. Additionally, anionic polystyrene nanoparticles (APNs) of 50 nm exhibit the greatest influence on M2 polarization. Proteomics was pursued to further understand the effect of NPs physicochemical parameters on protein corona, which revealed unique protein patterns based on NP charge and size. Several proteins impacting M1 and M2 macrophage polarization were identified within cationic polystyrene nanoparticles (CPNs) corona, while APNs corona included fewer M1 but more M2-promoting proteins. Nevertheless, size impacts protein corona abundance but not identities. Altogether, protein corona identities varied based on NP surface charge and correlated to dramatic differences in macrophage polarization. In contrast, NP size differentially impacts macrophage polarization, which is dominated by NP uptake level rather than protein corona. In this work, specific corona proteins were identified as a function of NP physicochemical properties. These proteins are correlated to specific macrophage polarization programs and may provide design principles for developing macrophage-mediated NP drug delivery systems.

Theoretical Description of Optofluidic Force Induction

Optofluidic force induction (OF2i) is an optical nanoparticle characterization scheme which achieves real-time optical counting with single-particle sensitivity and high throughput. In a recent paper [\ifmmode \check{S}\else \v{S}\fi{}imi\ifmmode \acute{c}\else \'{c}\fi{} et al., Phys. Rev. Appl. 18, 024056 (2022)], we have demonstrated the working principle for standardized polystyrene nanoparticles, and have developed a theoretical model to analyze the experimental data. In this paper we give a detailed account of the model ingredients, including the full working equations, provide additional justification for the assumptions underlying OF2i, and discuss directions for further developments and future research.

Individual and combined cytotoxicity effects of positively charged polystyrene nanoplastics and ionic surfactants on budding yeast Saccharomyces cerevisiae

It is of crucial importance to understand the impact of micro/nanoplastics contaminated with the other pollutants on microorganisms in the environment. In the present paper, we have investigated the individual and combined cytotoxicity effects of positively charged fluorescence-labeled polystyrene nanoparticles (pPS-NPs; 115 and 204 nm in diameter) and ionic surfactants [sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium chloride (C12TAC)] on budding yeast Saccharomyces cerevisiae after a short-time exposure (0.5 h) in a 5-mM NaCl aqueous solution. In the absence of surfactants, the smaller 115-nm pPS-NPs were more cytotoxic than the larger 204-nm pPS-NPs. In the absence of pPS-NPs, the cationic surfactant of C12TAC was more cytotoxic than the anionic surfactant of SDS, though these two ionic surfactants have the hydrophobic alkyl chains of the same length and the oppositely charged headgroups in the same magnitude. The addition of SDS decreased the number of pPS-NPs adhered on a negatively charged yeast cell to reduce the cytotoxicity, whereby the combined toxicity effect was considered as counteracting action. Although some addition of C12TAC hardly influenced the number of pPS-NPs adhered on a yeast cell, the synergistic cytotoxicity action of the pPS-NPs and C12TAC was observed.

Activation of FGF signal in germline mediates transgenerational toxicity of polystyrene nanoparticles at predicted environmental concentrations in Caenorhabditis elegans

Nanoplastics in the environment could cause the ecological and health risks. Recently, the transgenerational toxicity of nanoplastic has been observed in different animal models. In this study, using Caenorhabditis elegans as an animal model, we aimed to examine the role of alteration in germline fibroblast growth factor (FGF) signal in mediating the transgenerational toxicity of polystyrene nanoparticle (PS-NP). Exposure to 1–100 μg/L PS-NP (20 nm) induced transgenerational increase in expressions of germline FGF ligand/EGL-17 and LRP-1 governing FGF secretion. Germline RNAi of egl-17 and lrp-1 resulted in resistance to transgenerational PS-NP toxicity, indicating the requirement of FGF ligand activation and secretion in formation of transgenerational PS-NP toxicity. Germline overexpression of EGL-17 increased expression of FGF receptor/EGL-15 in the offspring, and RNAi of egl-15 at F1 generation (F1-G) inhibited transgenerational toxicity of PS-NP exposed animals overexpressing germline EGL-17. EGL-15 functions in both the intestine and the neurons to control transgenerational PS-NP toxicity. Intestinal EGL-15 acted upstream of DAF-16 and BAR-1, and neuronal EGL-15 functioned upstream of MPK-1 to control PS-NP toxicity. Our results suggested the important role of activation in germline FGF signal in mediating the induction of transgenerational toxicity in organisms exposed to nanoplastics in the range of μg/L.

Extraction of plastic nanoparticles using surface engineered kapok tubes from water

The nano- and microplastic particles from plastic wastes are emerging pollutants that cause significant harm to living organisms and the environment. Little is known on the removal of these emerging pollutants from water. The adsorbents reported to date have been designed to remove dissolved pollutants from water, such as dyes and heavy metals. Here, kapok tubes (KT) were modified and used for the removal of polymer nanoparticles from water. In order to enhance the interaction between the adsorbent surface and plastic particles in water, polyethyleneimine (PEI) was grafted onto the surface of the KT (PEI@KT). A series of techniques such as optical microscopy, FT-IR spectroscopy, scanning electron microscopy (SEM), elemental analysis, and thermal analysis were used to characterize KT and PEI@KT adsorbents. The adsorption of nanoparticles on the surface of the tubes was monitored using UV-Vis spectroscopy and electron microscopy. The modified fibers showed high removal rates (> 96 %) for negatively charged nanoparticles of polymethyl methacrylate (PMMA), polyvinyl chloride (PVC), and polystyrene (PS) within 90 min. Additionally, the factors affecting the adsorption of nanoparticles, isotherm, and kinetic models were explored to investigate the adsorption mechanism of polymer nanoparticles (PNPs) on the PEI@KT surface. The collected adsorption data fit well with the Langmuir isotherm and pseudo-second-order kinetic models. The adsorption capacities of PEI@KT for the three types of polymer nanoparticles were high (> 240 mg/g). As a proof of concept, PEI@KT was used to remove plastic microparticles from a diluted solution of a commercial body scrub gel with excellent adsorption and removal efficiencies. Overall, the environmentally friendly PEI@KT adsorbent showed high adsorption efficiencies toward removing plastic particles from water.

An Artificial Chameleon Skin for Dynamic Thermoregulation

AbstractSolar radiation is the major energy source for most living creatures, and some creatures change their skin colors responding to energy demands. Inspired by the chameleons that live in the desert of Namibia, which can regulate body temperature by changing skin colors between black and white, a patterned hydrogel film with self‐thermoregulation ability is reported in this work. The film consists of two parts: a light‐responsive black part and a stretchable white part. The black part is made of thermoresponsive poly(N‐isopropylacrylamide) hydrogel with polydopamine (PDA) nanoparticles, and the white part is made of stretchable polyacrylamide hydrogel with polystyrene (PS) nanoparticles. At low temperature and low light irradiation, the black part dominates the film, and the embedded melanin‐like PDA nanoparticles adsorb light and convert it to heat, thus reaching an active body temperature. At high temperature and strong light irradiation, the black part shrinks, which in turn stretches the white part to dominate the film, and more light is reflected by guanine crystals‐like PS nanoparticles, thus protecting body temperature from rising. The combination of the thermoresponsive black hydrogel and stretchable white hydrogel provides an evolutionary novelty that can control the solar lights for dynamic thermoregulation.

Polystyrene nanoplastics induce glycolipid metabolism disorder via NF-κB and MAPK signaling pathway in mice

Nanoplastics-induced developmental and reproductive toxicity, neurotoxicity and immunotoxicity are a focus of widespread attention. However, the effects of nanoplastics (NPs) on glycolipid metabolism and the precise underlying mechanisms are unclear at present. Here, we showed that oral administration of polystyrene nanoparticles (PS-NPs) disrupts glycolipid metabolism, with reactive oxygen species (ROS) identified as a potential key signaling molecule. After PS-NPs treatment, excessive production of ROS induced the inflammatory response and activated the antioxidant pathway through nuclear factor-erythroid factor 2-related factor 2. The activation of nuclear factor-κB (NFκB) signaling pathway induced the phosphorylation of the mitogen-activated protein kinases (MAPK) signaling pathway, which induced the activation of extracellular regulated kinases (ERK) and p38. Constitutive activation of the MAPK signaling proteins induced high continued phosphorylation of insulin receptor substrate-1, in turn, leading to decreased protein kinase B (Akt) activity, which weakened the sensitivity of liver cells to insulin signals and induced insulin resistance. In parallel, phosphorylation of Akt led to loss of control of FoXO1, a key gene of gluconeogenesis, activating transcription of glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PEPCK) in a manner dependent on PGC1α. Moreover, the activated ERK promoted lipid accumulation through ERK-PPARγ cascades. Therefore, sterol regulatory element-binding protein-1 and levels of its downstream lipogenic enzymes, ACC-1, were up-regulated. Upon treatment with the antioxidant resveratrol, PS-NPs-induced glucose and lipid metabolic disorders were improved by inhibiting ROS-induced activation of NFκB and MAPK signaling pathway in mice. Based on above, PS-NPs exposure disrupts glycolipid metabolism in mice, with ROS identified as a potential key signaling molecule.

Nanoplastics causes extensive congenital malformations during embryonic development by passively targeting neural crest cells

Nanomaterials are widespread in the human environment as pollutants, and are being actively developed for use in human medicine. We have investigated how the size and dose of polystyrene nanoparticles affects malformations in chicken embryos, and have characterized the mechanisms by which they interfere with normal development. We find that nanoplastics can cross the embryonic gut wall. When injected into the vitelline vein, nanoplastics become distributed in the circulation to multiple organs. We find that the exposure of embryos to polystyrene nanoparticles produces malformations that are far more serious and extensive than has been previously reported. These malformations include major congenital heart defects that impair cardiac function. We show that the mechanism of toxicity is the selective binding of polystyrene nanoplastics nanoparticles to neural crest cells, leading to the death and impaired migration of those cells. Consistent with our new model, most of the malformations seen in this study are in organs that depend for their normal development on neural crest cells. These results are a matter of concern given the large and growing burden of nanoplastics in the environment. Our findings suggest that nanoplastics may pose a health risk to the developing embryo.