Particulate Matter Elevates Ocular Inflammation and Endoplasmic Reticulum Stress in Human Retinal Pigmented Epithelium Cells

• Published in: International journal of environmental research and public health 2023-03, Vol.20 (6), p.4766
• Main Authors: Jeong, Sunyoung, Shin, Eui-Cheol, Lee, Jong-Hwa, Ha, Jung-Heun
• Format: Article
• Language: English
• Subjects: Adaptation; Air pollution; Air quality; Apoptosis; Calcium (intracellular); Calcium ions; Communication; Cytokines; Diabetic retinopathy; Drug dosages; Edema; Endoplasmic reticulum; Endoplasmic Reticulum Stress; Epidemiology; Epithelium; Epithelium - metabolism; Exposure; Gene expression; Humans; Hypoxia; Inflammation; Inflammation - chemically induced; Kinases; Life sciences; Macular degeneration; MAP kinase; Mitogen-Activated Protein Kinases; Molecular modelling; NF-kappa B - metabolism; NF-κB protein; Particulate emissions; Particulate matter; Particulate Matter - toxicity; Protein expression; Protein folding; Proteins; Retina; Retinal pigment epithelium; RNA; Scientific equipment and supplies industry; Stress
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph20064766

Because of their exposure to air, eyes can come into contact with air pollutants such as particulate matter (PM), which may cause severe ocular pathologies. Prolonged ocular PM exposure may increase inflammation and endoplasmic reticulum stress in the retina. Herein, we investigated whether PM exposure induces ocular inflammation and endoplasmic reticulum (ER) stress-related cellular responses in human retinal epithelium-19 (ARPE-19) cells. To understand how PM promotes ocular inflammation, we monitored the activation of the mitogen-activated protein kinase (MAPK)/nuclear factor kappa beta (NFκB) axis and the expression of key inflammatory mRNAs. We also measured the upregulation of signature components for the ER-related unfolded protein response (UPR) pathways, as well as intracellular calcium ([Ca ] ) levels, as readouts for ER stress induction following PM exposure. Ocular PM exposure significantly elevated the expression of multiple cytokine mRNAs and increased phosphorylation levels of NFκB-MAPK axis in a PM dose-dependent manner. Moreover, incubation with PM significantly increased [Ca ] levels and the expression of UPR-related proteins, which indicated ER stress resulting from cell hypoxia, and upregulation of hypoxic adaptation mechanisms such as the ER-associated UPR pathways. Our study demonstrated that ocular PM exposure increased inflammation in ARPE-19 cells, by activating the MAPK/NFκB axis and cytokine mRNA expression, while also inducing ER stress and stress adaptation responses. These findings may provide helpful insight into clinical and non-clinical research examining the role of PM exposure in ocular pathophysiology and delineating its underlying molecular mechanisms.