Microplastics have gained much attention due to their
prevalence
and abundance in our everyday lives. They have been detected in household
items such as sugar, salt, honey, seafood, tap water, water bottles,
and food items wrapped in plastic. Once ingested, these tiny particles
can travel to internal organs such as the kidney and liver and cause
adverse effects on the cellular level. Here, human embryonic kidney
(HEK 293) cells and human hepatocellular (Hep G2) liver cells were
used to examine the potential toxicological effects of 1 μm
polystyrene microplastics (PS-MPs). Exposing cells to PS-MPs caused
a major reduction in cellular proliferation but no significant decrease
in cell viability as determined by the trypan blue assay in both cell
lines. Cell viability remained at least 94% for both cell lines even
at the highest concentration of 100 μg/mL of PS-MPs. Phase-contrast
imaging of both kidney and liver cells exposed to PS-MPs at 72 h showed
significant morphological changes and uptake of PS-MP particles. Confocal
fluorescent microscopy confirmed the uptake of 1 μm PS-MPs at
72 h for both cell lines. Additionally, flow cytometry experiments
verified that more than 70% of cells internalized 1 μm PS-MPs
after 48 h of exposure for both kidney and liver cells. Reactive oxygen
species (ROS) studies revealed kidney and liver cells exposed to PS-MPs
had increased levels of ROS at each concentration and for every time
point tested. Furthermore, quantitative reverse transcription polymerase
chain reaction (qRT-PCR) analysis at 24 and 72 h revealed that both
HEK 293 and Hep G2 cells exposed to PS-MPs lowered the gene expression
levels of the glycolytic enzyme,
glyceraldehyde-3-phosphate
dehydrogenase
(
GAPDH
), and antioxidant enzymes
superoxide dismutase 2
(
SOD2
) and
catalase
(
CAT
), thus reducing the potential
of SOD2 and CAT to detoxify ROS. These adverse effects of PS-MPs on
human kidney and liver cells suggest that ingesting microplastics
may lead to toxicological problems on cell metabolism and cell–cell
interactions. Because exposing human kidney and liver cells to microplastics
results in morphological, metabolic, proliferative changes and cellular
stress, these results indicate the potential undesirable effects of
microplastics on human health.