We can't find the internet
Attempting to reconnect
Something went wrong!
Hang in there while we get back on track
Bioelectric Changes in Primary Rat Alveolar Epithelial Cell Monolayers Exposed to Various Nanoplastics
AI summary Read the abstract
Primary rat alveolar epithelial cells were exposed to various nanoplastic particles to measure changes in bioelectric properties, an indicator of barrier integrity and ion transport. Results showed nanoplastic-induced disruptions to monolayer bioelectric properties, suggesting nanoplastics can impair lung epithelial function.
Introduction: About 0.25 megatons of plastic waste from consumer and industrial sources found in waterways, including sub-millimetric plastic particles generated from environmental degradation, may pose significant health risks. The biological and ecological impacts of materials <1 μm (nanoplastics) are of particular concern because they are generally too small for most conventional filtration processes and challenging to collect, detect and identify. Furthermore, their high surface area-to-volume ratio makes them efficient carriers for toxic substances. Despite this, most of the studies in recent literature reviews employed manufactured nanoplastics of uniform size and shape, which do not reflect actual environmental plastic waste. A systematic analysis of environmental nanoplastic impacts on biota would be vital in understanding the full life cycle of plastic pollution. In this study, we investigated how different nanoplastics affect the ion transport properties of lung alveolar epithelium. Methods: We crushed and pulverized cuvettes (polystyrene (PS)), droppers (polyethylene (PE)), centrifuge tubes (polypropylene (PP)), and containers (polyethylene terephthalate (PET)) prior to irradiation and ozone treatment. These nanoplastics in water were twice-filtered with 800 nm polyethersulfone filters and concentrated by evaporation. The resulting nanoplastic solids were weighed and re-suspended in 1 mL mQ water. They were then ultrasonicated for 15 minutes to break up any aggregates. We measured size distribution, surface charge and shape of the nanoplastics using a zeta sizer/DLS and electron and/or confocal microscopy. For ease of detection, these nanoplastics were also stained with Rhodamine B by heat swelling at 70°C for several hours, followed by dialysis or size-exclusion chromatography to remove unbound dye. Commercial 20 nm spherical polystyrene nanoparticles (PNP) with -10 mV zeta potential were used for comparison purposes. Effects of nanoplastics and PNP on primary cultured rat alveolar epithelial cell monolayers were studied by measuring transepithelial resistance (Rt) and spontaneous potential difference (PD) for up to 48 hours after adding nanomaterials to the apical fluid of the monolayers, while control monolayers received only culture fluid apically. Active ion transport rate (Ieq) was estimated as the ratio PD/Rt. Results: Typical size, polydispersity (%PD), morphology and absolute value of zeta potential for our nanoplastics are 120-350 nm, 11-25%, dendritic and 10-13 (±8) mV. PNP exposure led to a rapid decrease in Rt by ~70% at 30 minutes and a slow return to control level thereafter, whereas Ieq decreased by ~50% at 30 minutes and returned to control level very slowly. PP exposure also led to rapid fall in Rt by ~60% with very slow return to control level, but without an effect on Ieq. PS resulted in a slower decrease in Rt by ~40% at 8 hours, followed by return to control level by 48 hours, without affecting Ieq. The other nanoplastics (PE and PET) tested did not cause significant changes in either Rt or Ieq following apical exposure. Conclusions: These observations are consistent with the hypothesis that the material, size, shape and surface charge of nanomaterials influence their effects on the bioelectric properties of the alveolar epithelium. This abstract was presented at the American Physiology Summit 2025 and is only available in HTML format. There is no downloadable file or PDF version. The Physiology editorial board was not involved in the peer review process.
More Papers Like This
In-house Fabrication of Nanoplastics of Tunable Composition and Application: Assessment of Bioelectric Changes in Primary Rat Lung Alveolar Epithelial Cell Monolayers Exposed to Nanoplastics
AI summary Read the abstract
Researchers developed standardized methods for fabricating nanoplastics of tunable composition in the lab, then used these particles to assess bioelectric changes in primary rat lung alveolar epithelial cell monolayers. The study found that nanoplastic exposure altered the electrical properties of lung cells, suggesting that inhaled nanoplastics may disrupt the lung epithelial barrier function.
Developing a model to test microplastic impact on lung epithelial barriers formation and functionality
AI summary Read the abstract
Researchers developed an air-liquid interface lung epithelial model using A549 cells on PET inserts to evaluate the impact of PET and polystyrene microplastics on the human lung barrier, characterizing transepithelial electrical resistance and permeability over time to establish a stable barrier model more representative of natural alveolar conditions than standard submerged culture.
Nanoelectrochemistry monitoring of intracellular reactive oxygen and nitrogen species induced by nanoplastic exposure
AI summary Read the abstract
Researchers used tiny nanoelectrodes to measure reactive oxygen and nitrogen species inside lung cells exposed to nanoplastics. They found that nanoplastic exposure significantly increased nitrogen-based reactive species while oxygen-based species remained relatively stable. The study provides new evidence about the specific types of oxidative stress that airborne nanoplastics can trigger inside human cells.
Nanoplastic-induced Disruption of DPPC and Palmitic Acid Monolayers: Implications for Membrane Integrity
AI summary Read the abstract
Polystyrene nanoplastics were found to disrupt DPPC and palmitic acid lipid monolayers—models of lung alveolar and cell membranes—suggesting that inhaled or ingested nanoplastics could compromise lung alveolar stability, cell signaling, nutrient delivery, and potentially cause neurotoxicity through membrane disruption.
Toxicological effects of different particle sizes and types of nano-plastics (NPs) on human lung cells: implications for the health risk of airborne microplastic pollution
AI summary Read the abstract
Researchers exposed human A549 alveolar cells to polystyrene and polymethylmethacrylate nanoplastics of 30 and 50 nm and found that smaller size and higher concentration produced stronger cytotoxicity, oxidative stress, inflammation, and apoptosis—with PS nanoparticles more toxic than PMMA—providing in vitro evidence of respiratory health risks from inhaled airborne nanoplastics.
Research digests by email
When a large batch of papers lands in the Atlas, we read through it and send a short write-up of what stood out.