Polystyrene and Polyethylene Microplastics Decrease Cell Viability and Dysregulate Inflammatory and Oxidative Stress Markers of MDCK and L929 Cells In Vitro.
Swetha PalaniappanChakravarthy Marx SadacharanBahman RostamaPublished in: Exposure and health (2021)
Microplastics are ubiquitous environmental pollutants that are a growing concern to many ecosystems, as well as human health. Many of the effects of microplastics on mammalian cells and tissues remain unknown. To address this, we treated L929 murine fibroblasts and Madin-Darby canine kidney (MDCK) epithelial cell lines with 1 μg/mL, 10 μg/mL, or 20 μg/mL of polyethylene (PE) or polystyrene (PS) microspheres in vitro for 6 and 24 h and measured the resulting changes in cell viability, metabolism, and transcriptional expression of inflammatory cytokines and antioxidant enzymes. We observed dose-dependent decreases in cell viability corresponding to increases in doses of both PE and PS. We conducted cell metabolism assays and observed dose-dependent increases in metabolism per cell with increasing doses of both PE and PS. Similarly, we also observed increased expression of the superoxide dismutase-3 gene (SOD3), indicating oxidative stress caused by the microplastics treatments. We also observed increased expression of TNFα, but decreased expression of IFNβ, suggesting different mechanisms by which the microplastics regulate inflammatory responses in mammalian cells. Our results contribute new data to the growing understanding of the effects of microplastics on mammalian cells and indicate complex cellular stress responses to microplastics in the environment.
Keyphrases
- human health
- oxidative stress
- risk assessment
- poor prognosis
- climate change
- induced apoptosis
- gene expression
- binding protein
- rheumatoid arthritis
- dna damage
- immune response
- cell therapy
- single cell
- high throughput
- ischemia reperfusion injury
- copy number
- dendritic cells
- high resolution
- bone marrow
- electronic health record
- mesenchymal stem cells
- extracellular matrix
- mass spectrometry
- amyotrophic lateral sclerosis
- big data
- heat shock protein