Identification of miRNAs induced by low-dose methylmercury exposure and their roles in inflammatory responses using human aortic endothelial cells.
- Author:
Rika MATSUYAMA
1
;
Athira NANDAKUMAR
1
;
Munekazu YAMAKUCHI
2
;
Saekhol BAKRI
1
;
Shiroh TANOUE
1
;
Mayumi TSUJI
3
;
Megumi YAMAMOTO
4
;
Teruto HASHIGUCHI
2
;
Chihaya KORIYAMA
1
Author Information
- Publication Type:Journal Article
- Keywords: Cyclooxygenase-2; Human aortic endothelial cells; Inflammation; Methylmercury; MicroRNAs
- MeSH: Methylmercury Compounds/adverse effects*; Humans; MicroRNAs/genetics*; Endothelial Cells/metabolism*; Inflammation/genetics*; Cell Line; Aorta/drug effects*; Biomarkers/metabolism*
- From:Environmental Health and Preventive Medicine 2025;30():93-93
- CountryJapan
- Language:English
-
Abstract:
BACKGROUND:Exposure to methylmercury (MeHg) is predominantly attributed to consumption of marine products. However, the general population is exposed to low MeHg levels, which can induce chronic inflammation. Although some MeHg-related microRNAs (miRNAs) have been reported, their functions remain elusive. The objective of this study was to identify the miRNAs induced by low-level MeHg exposure in a human endothelial cell line (HAECs). This study aimed to determine the specific miRNAs induced by low-level MeHg exposure using a HAECs as a potential novel and sensitive biomarker. The roles of miRNAs in inflammatory processes have been examined.
METHODS:Using HAECs, a miRNA microarray assay was performed to identify miRNAs with altered expression upon exposure to a non-cytotoxic MeHg level (0.1 and 1.5 µM). The expression patterns of interleukin-6 and -8, cyclooxygenase 2 (COX-2), RelB, and prostaglandin E2 (PGE2) were examined after transfection of the identified miRNAs with mimics/inhibitors.
RESULTS:Although the microarray assay identified six MeHg-specific miRNAs, miR-3613-5p, upregulated by 0.1 and 1.5 µM MeHg exposures, demonstrated the best reproducibility in HAECs. Transfection with the miR-3613-5p mimic enhanced the MeHg-induced inflammatory responses, including PGE2 and COX-2 protein levels, whereas the miR-3613-5p inhibitor suppressed these inflammatory responses.
CONCLUSION:This study observed that miR-3613-5p is induced by low-dose MeHg exposure, plays a crucial role in the inflammatory process, and could serve as a novel and sensitive biomarker for low-level MeHg exposure.
