1. Introduction
After decades of environmental pollution with various plastic litter, concerns are growing that the rising global plastic burden might affect marine and terrestrial life. However, production and consumption of plastics are continuously increasing [
1], leading to the accumulation of plastic debris around the globe [
2]. Particular attention is being given to small plastic particles which can derive from different sources; primary plastic particles are introduced into freshwater and saltwater as manufactured microscale polymers, commonly found in cosmetic care products and medications [
3], while secondary particles are generated through the ongoing fragmentation of plastic waste [
4]. A significant portion of secondary plastic particles originates from public litter, improper waste disposal by the fishing industry [
4], sewage water containing plastic particles from washing synthetic textiles [
5], and tire abrasion [
6]. Environmental impacts lead to the creation of microplastic (MP) particles measuring less than 5 mm in diameter, which can subsequently break down into even smaller nanoplastic (NP) particles [
7]. The definition and size range of nanoplastics remain subjects of debate within the scientific community. While the commonly accepted size limit is under 100 nm, some extend this range up to 1000 nm. Plastic residues have been found extensively worldwide, spanning beaches, shores, freshwater and saltwater bodies, deep-sea sediments, and even within Antarctic sea ice [
7].
Although most studies examining the impact of plastic particles on the environment have focused on the marine ecosystem, plastic contamination may be more widespread in the terrestrial ecosystem and human diet than previously anticipated. Small plastic particles are consumed by aquatic organisms [
8], entering the circulatory systems of marine wildlife. Subsequently, they propagate throughout the marine food chain, ultimately contaminating seafood intended for human consumption [
9]. Moreover, plastic packaging used for beverages and food is an obvious source of ingested NP and MP particles [
10]. Thermal stress can induce the migration of small plastic particles into food; however, exposure estimates need to be validated and testing methods need to be standardized in order to perform comprehensive risk assessments [
11]. However, MP particles have also been detected in tap water, honey, sugar, sea salt, and beer [
12,
13,
14,
15,
16]. It is estimated that an average adult consumes approximately 39,000 to 52,000 particles per year [
17]. Other studies estimate that humans consume between 0.1 and 5 g of plastic each week, which is roughly equivalent to a credit card-sized amount of plastic [
18]. Unsurprisingly, microplastics have been detected in human feces [
19] and blood [
20].
NP particles possess high bioavailability due to their small diameter [
21,
22]. It is expected that synthetic particles with a diameter below 130 µm can cross the gastrointestinal barrier via paracellular transport [
21,
23], while particles smaller than 10 µm may be absorbed by microfold cells [
21,
24], where they are passed to intestinal macrophages. Macrophages are immune phagocytes with the capacity to efficiently clear foreign-body particles. In the gastrointestinal tract, macrophages patrol along the intestinal epithelium, where they sense and eliminate bacterial products and foreign-body particles that surpass the intestinal epithelial barrier [
25]. They play crucial roles in the innate immune system and maintain immune balance. Thus, macrophages are at the front line of host defense and are expected to be the first immune cells to encounter ingested NP or MP particles in the intestine. However, the impact of NPs and MPs on macrophages still needs to be investigated.
Despite the rising global abundance of small plastic particles and increasing awareness, plastic research is still in its early stages, and the potential impact of exposure to NPs and MPs on human health remains unpredictable. As the consumption of small plastic particles continues to increase along with rising levels of plastic in the human diet, the toxicity risks could escalate due to the accumulation of these particles in the body. Since particles with smaller diameters are believed to penetrate epithelial barriers more easily [
21,
24]; nanosized plastic particles are anticipated to have high bioavailability, facilitating increased translocation into the system.
Thus, studying the effects of plastic exposure on human health is of great public interest. Individuals with chronic intestinal inflammation, such as inflammatory bowel disease (IBD), could be especially susceptible to the harmful effects of ingested plastic particles. This vulnerability arises because disruptions and increased permeability of the intestinal epithelial barrier [
26] may enable greater translocation of MP and NP particles into the systemic circulation compared to healthy individuals. While initial in vivo studies report proinflammatory and adverse health effects in rodents upon oral exposure to MP particles [
27,
28,
29,
30,
31], data on NP particles are very limited and require closer investigation. Here, we evaluate the impact of NP particles on macrophages and intestinal health in homeostasis and during the development of intestinal inflammation.
2. Materials and Methods
2.1. Ethical Considerations
Animal experiments were carried out in compliance with Swiss animal welfare laws and approved by the local veterinary office (Veterinary Office of the Canton Zurich; License 019/2018). Wildtype mice on a C57BL/6 background were bred and housed in a specific pathogen-free (SPF) facility with unrestricted access to standard chow and water.
2.2. Isolation and Cultivation of Bone Marrow-Derived Macrophages
Bone marrow was isolated from 8-week-old mice, homogenized with an 18 gauge needle, and passed through a 70 µm cell strainer, as previously described [
32]. Cells were seeded in noncoated Petri dishes at a density of 3 × 10
6 cells in 10 mL RPMI 1640 media (Thermo Fisher Scientific, Waltham, MA, USA), supplemented with 10% FCS (#S181T-500, Biowest, Nuaillé, France), 1 mM Sodium Pyruvate (Thermo Fisher Scientific), 1 mM L-Glutamine (Thermo Fisher Scientific), 50 units/mL penicillin and 50 µm/mL streptomycin (Thermo Fisher Scientific), and 20 ng/mL recombinant mouse MCSF (#576408, BioLegend), and cultivated at 37 °C, 10% CO
2. Media were replaced on day 5 post isolation. On day 7, cells were detached from the Petri dishes using Accutase (StemCell, Köln, Germany) and seeded in 6-well plates at a density of 3 × 10
6 cells in 5 mL RPMI media per well. Macrophage differentiation was confirmed by flow analysis, quantifying the expression of the pan-macrophage marker F4/80, which was present in 93% of all cells. Bone-marrow-derived macrophages (BMDMs) were exposed to green-fluorescent NP particles (Micromer greenF plain 25 nm polymethacrylate particles #29-00-251, spheric, suspension in water, Micromer greenF plain 50 nm polystyrene particles #29-00-501, spheric, suspension in water, Micromod, Rostock, Germany) diluted in RPMI media at a concentration of 100 µg/mL, 200 µg/mL, and 400 µg/mL. After incubation for 2 h, 4 h, 8 h, or 24 h, cells were rinsed with PBS twice and scraped off the surface in 200 µL homogenization buffer containing thiogylcerol (#AS1390, Promega, Madison, WI, USA). Bright-field images of the treated cells were taken using a Nikon ECLIPSE Ts2 microscope (Nikon, Düsseldorf, Germany).
2.3. RNA Isolation, RT-PCR, and Real-Time PCR
RNA was extracted using the Maxwell RSC simplyRNA Tissue kit and Maxwell RSC instrument (Promega, Walldorf, Germany), following the manufacturer’s guidelines. RNA concentration was determined by measuring absorbance at 260 nm and 280 nm using a Nanodrop 1000 spectrophotometer (Thermo Fisher Scientific). Complementary DNA (cDNA) was synthesized using the High-Capacity cDNA Reverse Transcription Kit (Thermo Fisher Scientific). Gene expression analysis utilized predesigned TaqMan Real-Time PCR Assays and TaqManTM FAST Universal PCR Master Mix on a QuantStudio 6 Flex Real-Time PCR System, following the manufacturer’s protocols (all reagents purchased from Thermo Fisher Scientific). Measurements were conducted in triplicate, and results were normalized to murine Actb (Thermo Fisher Scientific) as an endogenous control, analyzed using the ∆∆CT method.
2.4. IF Staining and Confocal Microscopy
BMDMs were differentiated as described above and seeded on glass coverslips before treatment with green-fluorescent 25 nm or 50 nm NP particles (Micromer greenF plain 25 nm polymethacrylate particles #29-00-251, Micromer greenF plain 50 nm polystyrene particles #29-00-501, Micromod) diluted in RPMI at a concentration of 100 ug/mL. Following a 24 h incubation period, cells were fixed with 4% paraformaldehyde for 20 min, washed three times with PBS, and then blocked in PBS containing 10% normal goat serum (NGS) and 5% bovine serum albumin (BSA). Cells were incubated with Phalloidin iFluor 647 (#ab176759, Abcam, Cambridge, UK) and DAPI diluted in PBS, 1% NGS, and 1% BSA for 1 h at room temperature. Coverslips were washed in PBS three times and shortly dipped in ultrapure water before mounting on glass slides using fluorescence mounting media (Agilent Technologies, Santa Clara, CA, USA). Fluorescent-labeled cells were examined using the LEICA SP8 Upright equipped with a PL Fluotar 40× oil objective (Leica Microsystems, Wetzlar, Germany). Images were processed using the LAS X (Leica) and Imaris 9.3 software (Oxford Instruments, Abingdon, UK).
2.5. Mice and In Vivo Treatments
Study design: Appropriate control groups were included in all experiment. Since the DSS and PMMA NP particles were supplied in the drinking water, each cage was considered as an experimental unit. Female C57Bl6 WT mice (3 weeks old) were used for all experiments. Long-term administration: In this setup, a relative low variance was expected within each group. Assuming a difference of 30% between treatment groups and controls, considering 6 groups to be compared, and a required power of 80% including an alpha error of 0.05, ANOVA resulted in a group size of 10 animals per group. Acute DSS colitis: Within this setup, a medium variance was expected within each group. Assuming a difference of 30% between treatment groups and controls, considering 6 groups to be compared, and a required test power of 80% including an alpha error of 0.05, ANOVA resulted in a group size of 20 animals per group. Terminal evaluation of inflammation was performed in a blinded manner. The here-described experiments are confirmatory. Primary outcome: MEICS score (0–15 with 0.5 increments). Additional outcome: Weight change, histology score, colon length, spleen weight, barrier integrity. The null hypothesis posits that there is no difference among the means of all groups. The alternative hypothesis is that at least one of the paired comparisons would change the colitis score. Since colitis induction is influenced by the weight, the mice underwent stratified randomization according to their body weight prior to the start of the DSS treatment. The concentration of DSS used in this study was determined based on our group’s experience and recent experiments. It was selected to induce moderate colitis, enabling the detection of any potential exacerbating effects of PMMA particle administration on the disease.
Termination criteria during the study: Appearance: elevated (orifices clearly clotted, abnormal body posture); behavior: elevated (almost no movement); stool consistency: liquid; blood in stool: rectal blood loss; weight loss since start of the experiment: ≥20%. The sample size was determined by the number of female animals that were retrieved in our breedings. Due to animal welfare reasons we decided to refrain from using additional animals, as plastic administration clearly showed no effect in the conducted experiments.
Sample size: long-term administration: 16 weeks: Ctrl: n = 8, NP: n = 8; 20 weeks: Ctrl = 8, NP = 8; 24 weeks: Ctrl = 8; NP = 9. One mouse from 20 weeks NP and 24 weeks Ctrl had to be removed from the experiment due to elephantiasis. No MEICS score and barrier integrity assay from one mouse 24 weeks NP due to sudden death during anesthesia induction. Acute DSS colitis: H2O: n = 7; DSS: n = 16; NP: n = 8; DSS NP: n = 16. DSS: No MEICS score from one mouse as it died during anesthesia induction. From one mouse in the DSS NP group, a histology score could not be assigned as tissue section could not be evaluated due to technical issues.
Immediately after weaning, mice were supplemented with 25 nm polymethacrylate (PMMA) particles (Micromer plain 25 nm polymethacrylate particles #01-00251, spherical, suspended in water, Micromod). Transmission electron microscopy (TEM) images of the particles are shown in
Figure S1A. Nanoparticles (NPs) were provided in the drinking water at a concentration of 0.05 mg/mL, resulting in an average daily consumption of approximately 0.2 mg per mouse, based on an average daily water intake of 4 mL per mouse. For long-term administration, mice were exposed to NP particles for 4, 5, and 6 months with staggered termination. In colitis experiments, mice were pretreated with NP particles for 6 months before induction of colitis. Colitis was induced by administering 1.5% DSS (#9011-18-1, MP Biomedicals, Santa Ana, CA, USA) in drinking water for 7 days, followed by 3 days of normal drinking water. Control mice received normal drinking water with or without PMMA particles but did not receive DSS. NP particles were administered throughout the entire experiment. Female WT mice (n = 8 per condition) were used for in vivo experiments. Average water consumption within each group was monitored daily during the initial 14 days of the experiment and subsequently twice a week. Average consumption of drinking water throughout the experiments is depicted in
Supplementary Figure S1C,D. Water bottles of the respective experimental groups were weighed and divided by the number of days between measurements and the number of animals per cage. Prior to DSS administration, control and NP groups were randomized based on body weight. The concentration of DSS used in this study was determined based on our group’s experience and recent experiments, chosen to induce moderate colitis, facilitating the detection of potential exacerbating effects of PMMA particle administration on the disease. Water consumption was not affected by the presence of NP particles or DSS. Drinking water and bottles with or without DSS and NPs were replaced twice a week. Bottles were agitated daily to ensure even distribution of NPs in the drinking water. No biosurfactant was utilized and, according to the manufacturer’s product information, the purchased particles were free of surfactants. NP particles remained well dispersed in the drinking water, as confirmed by dynamic light scattering (DLS) experiments conducted over 48 h (
Figure S1B). Since DSL and TEM delivered divergent data with respect to particle size, corona formation around the particles in the drinking water cannot be excluded. However, this cannot be evaluated as the extent of protein/inorganic content in the drinking water of the animal husbandry was not analyzed. Visually, no aggregation or sedimentation of particles was observed during the experiments.
2.6. FITC-Dextran Assay
On the final day of the experiment, mice underwent a 2 h fasting period (no food but water ad libitum) before receiving an oral gavage of 200 µL FITC-dextran (80 mg/mL, #46944-500MG-F Fluorescein isothiocyanate-dextran average molecular weight 4000, Sigma Aldrich, St. Louis, MO, USA). Five hours after gavage, mice were anesthetized by intraperitoneal injection of ketamine (90–120 mg/kg body weight, Vétoquinol, Bern, Switzerland) and xylazine (8 mg/kg body weight, Bayer AG, Leverkusen, Germany), and blood was collected retrobulbarly into serum collection tubes. The blood was centrifuged at room temperature for 5 min at 8000× g and diluted 1:5 with PBS (pH 7.4). Serum FITC-dextran concentration was measured in triplicate at an excitation wavelength of 485 nm and an emission wavelength of 535 nm. Standard curves for calculating FITC-dextran concentration in the samples were generated by diluting FITC-dextran in serum from nongavaged mice (0, 125, 250, 500, 1000, 2000, 4000, 8000 ng/mL) diluted in PBS.
2.7. Assessment of Colitis Severity
Colonoscopy was conducted on anesthetized mice using the Video-Uretero-Renoskop FLEX-X C IMAGE1 STM camera system (Karl Storz SE & Co. KG, Tuttlingen, Germany), following established procedures [
33]. Colitis severity was evaluated using the murine endoscopic index of colitis severity (MEICS) scoring system, which considers five parameters: (i) transparency of the colon wall, (ii) changes in the vascular pattern, (iii) presence of fibrin, (iv) granularity of the mucosal surface, and (v) stool consistency. Mice were euthanized to assess spleen weight and measure colon length. Epithelial damage and inflammatory infiltrates were evaluated using H&E-stained sections of the most distal 1 cm of the colon, and scoring was performed according to established methods [
34]. Both colonoscopy and histological evaluations were conducted by two independent researchers.
2.8. H&E Staining
The distal 1 cm segment of the colon was fixed in 4% formalin and subsequently embedded in paraffin. Sections of 5 µm thickness were deparaffinized using Histoclear (Chemie Brungschwig, Basel, Switzerland) and rehydrated through a descending series of alcohol. H&E staining was conducted following standard protocols and analyzed with Imager.Z2 and ZenPro 2.0 software (Zeiss, Oberkochen, Germany).
2.9. Statistics
Statistical analyses were conducted using two- or one-way ANOVA with Tukey’s multiple comparisons for parametric data and the Kruskal–Wallis test for nonparametric data. Results are presented as mean ± SEM, and significance was defined as p < 0.05.
4. Discussion
Plastic pollution poses one of the biggest challenges of our time. Despite growing evidence that the plastic contamination in our food might be more pervasive than expected [
12,
13,
14,
15,
16,
17,
18], there have been limited studies exploring the effects of ingested plastic particles on human health, and data on NP particles are very controversial. With plastic pollution escalating worldwide, it is evident that understanding the effects of plastic exposure on the human body, particularly on the digestive system, is crucial. In this study, we examined the influence of NP particles on gastrointestinal health both in vitro and in vivo.
Our study investigated the impact of nanoparticle (NP) exposure on bone-marrow-derived macrophages (BMDMs) and its implications for gastrointestinal health. The exposure of BMDMs to 25 nm PMMA or 50 nm PS particles led to notable morphological changes, including a shift to a spherical shape and increased detachment from culture plates, suggesting that NP particles can substantially modify the cellular structure of macrophages. In addition to morphological changes, NP exposure also triggered an inflammatory response in BMDMs. Contrary to the in vitro findings, long-term exposure to 25 nm PMMA particles in drinking water did not adversely affect gastrointestinal health or homeostasis in WT mice. Measures of weight gain, colonoscopy, histology, and epithelial barrier integrity remained unchanged compared to controls. Furthermore, NP administration did not exacerbate acute colitis induced by DSS, with similar outcomes in weight loss, colon length, and spleen weight across treatment groups. These results suggest that while NP exposure induces significant inflammatory and morphological changes in BMDMs in vitro, it does not appear to disrupt gastrointestinal homeostasis or worsen DSS-induced colitis in vivo. This discrepancy might be attributed to the differences in NP concentrations, exposure duration, or the complexity of the in vivo environment compared to cell culture conditions. Additionally, Raman spectroscopy did not detect NP particles in the intestine or distant organs, indicating that the particles might not persist or accumulate in significant amounts. Overall, our findings provide insight into the cellular impact of NP exposure and suggest that while NP particles can induce an inflammatory response in macrophages, their long-term ingestion does not necessarily impair gastrointestinal health or exacerbate inflammatory conditions in mice. Further studies are warranted to explore the broader implications of NP exposure on different biological systems and chronic health outcomes.
Macrophages respond to foreign particles that breach the intestinal epithelial barrier by engulfing and clearing them from the system through phagocytosis [
25]. Here, we showed that NPs engulfed by macrophages cause morphological alterations in these cells. Moreover, NP administration leads to increased expression of proinflammatory cytokines such as
Tnfa,
Il6, and
Il12b, along with alterations in the expression profiles of costimulatory molecules
Cd80 and
Cd86. These changes indicate a proinflammatory response following exposure to plastics. In line with our experiments, a recent study by Banerjee et al. reported cell death due to oxidative stress, membrane damage, immune response, and DNA damage in mammalian cells treated with NP or MP particles [
36]. Those adverse effects increased significantly with small particle size, the positive charge of the particles, high administration dose, and longer incubation times and were more severe when the particles were loaded with surfactants or adsorbed pollutants [
36]. The process of engulfing nanoplastics might alter the physical state of macrophages, affecting their cytoskeleton and, thus, their ability to migrate. The energy and resources spent on phagocytosing nanoplastics might also reduce their capacity to move and respond to other stimuli. This might have severe impacts on macrophage function and innate immune response.
Contrary to the strong effects on macrophages observed in vitro, long-term NP administration in vivo had no adverse impacts on the gastrointestinal health of mice, nor did it aggravate experimental intestinal inflammation. Previously, plastic research predominantly centered on the impacts of plastic contamination in marine and freshwater ecosystems, using fish, mollusks, or crustaceans as model organisms [
37], whereas information on the toxicity of NP particles in mammalian systems is highly limited. Initial studies investigating the effects of NP ingestion in mice reported alterations of gut microbiota and mucus secretion [
27,
38], impairment of the barrier integrity [
39,
40], intestinal damage, acute inflammation, and oxidative stress [
41,
42,
43]. Yang et al. recently reported aberrant macrophage polarization and activation upon PS nanoplastic exposure, resulting in IL1β secretion, altered T-cell response, and, ultimately, adverse impacts on brain function [
44,
45]. However, these studies used relatively high amounts of plastic particles within a short duration, which may not reflect realistic conditions. In contrast, we opted for physiological conditions that closely mimic the in vivo situation observed in healthy individuals or patients suffering from inflammatory bowel disease (IBD). In our studies, we used methacrylate particles, which find use as raw material in the production of many plastics. In humans, exposure to plastic typically begins within the first few months after birth, as babies are fed milk and, later, other beverages from plastic baby bottles [
46]. The first and most significant peak in the onset of IBD occurs in late adolescence and early adulthood at the age between 15 and 30 years. Building on these observations, we initiated pretreatment of mice with NP and MP particles immediately after weaning and induced acute DSS colitis following long-term exposure to plastic particles for 6 months. The presence of MPs in placental tissue suggests that plastic exposure may even commence during fetal development through the transfer of small plastic particles from mother to unborn child [
47], raising significant concerns. Our study design was based on the infamous data extraction study conducted at the University of Newcastle, Australia, which indicated that individuals later consume approximately 5 g of small plastic particles per week, totaling over 250 g annually [
18]. Scaling down this amount to the average size of a mouse, we administered a corresponding daily dose of 0.2 mg of NP particles. For our model, we chose to administer plastic particles via drinking water to enable consistent distribution of the dose throughout the day. However, estimates of human plastic consumption vary widely depending on the methodologies used in different studies. While some research suggests that humans consume small but significant amounts of plastic weekly, others argue that these estimates may be imprecise or based on limited data. Furthermore, it is not known which fraction of the ingested plastic is nanosized. Moreover, unlike our model, real-life human exposure involves a dietary-related mixture of NP and MP particles of varying sizes and types, although there is currently no data available on the composition of the ingested plastic burden. Nevertheless, it would be interesting to test how a mixture of different plastic particles coated with other materials such as pollutants or heavy metals might affect intestinal and whole-body health.
Detection of micro- and, especially, nanosized plastic particles in human or murine tissue remains challenging, and plastic research is lacking uniform and consistent methods. Despite intense research on the development of plastic particle detection and identification methods, there is currently no reliable and well-established methodology available that would enable the detection of PMMA nanoparticles in murine tissue. Therefore, we cannot conclude whether the absence of in vivo effects is a result of the possibility that the NP particles are not surpassing the intestinal epithelium and are subsequently excreted, or whether they are penetrating into the mucosa and simply do not affect gut homeostasis or inflammation—this is certainly the biggest limitation of this study. While Raman spectroscopy enabled the detection of NP and MP particles in tissue lysates in a previous study from our lab [
35], the administered PMMA particles could not be evidenced clearly following the same approach. This might be attributed by the chemical structure differences between PMMA and PS. PS contains a phenol ring, which results in a prominent Raman peak at approximately 1000 nm Raman shift, while PMMA does not exhibit such a characteristic intense peak. With the development of advanced spectral analysis techniques, such as machine learning-based algorithms, it may be possible in the near future to accurately identify these polymers even in cases where their characteristic peaks are not as pronounced.