DNMT1 regulates miR-20a/TXNIP-mediated pyroptosis of retinal pigment epithelial cells through DNA methylation

• Published in: Molecular and cellular endocrinology 2023-11, Vol.577, p.112012-112012, Article 112012
• Main Authors: Xi, Xiaoting, Wang, Min, Chen, Qianbo, Ma, Jia, Zhang, Junyan, Li, Yan
• Format: Article
• Language: English
• Subjects: Diabetic retinopathy; DNMT1; miR-20a/TXNIP; Pyroptosis; Retinal pigment epithelium cells
• ISSN: 0303-7207; 1872-8057
• DOI: 10.1016/j.mce.2023.112012

Pyroptosis of retinal pigment epithelium (RPE) cells is associated with the etiology of diabetic retinopathy (DR). In this study, we investigated the effect of DNMT1 on RPE cell pyroptosis by regulating miR-20a/TXNIP expression through DNA methylation. High glucose (HG)-induced ARPE-19 cells and mice were injected with streptozotocin (STZ) to generate DR cells and animal models. RT‒qPCR was used to detect the expression of miR-20a, and methylation-specific PCR (MS-PCR) was used to determine the occurrence of methylation of miR-20a. The expression of pyroptosis-related proteins (caspase-1 and NLRP3) and DNA methyltransferase (DNMT1) was detected by western blotting, and the expression of inflammatory factors (IL-1β and IL-18) was detected by ELISA. Apoptosis was detected by flow cytometry and TUNEL. HE staining was used to observe the pathological changes in retinal tissue in mice. In HG-induced DR cell models, the expression of miR-20a was significantly downregulated, while the expression of inflammatory factors (IL-1β, IL-18) and pyroptosis-associated proteins (caspase-1, NLRP3) was significantly upregulated. Transfection of miR-20a mimic can effectively reverse HG-induced pyroptosis and release of inflammatory factors. DNMT1 promotes miR-20a methylation and inhibits the expression of miR-20a. DNMT1-mediated methylation is involved in the pyroptosis process of high glucose-induced RPE cells, and silencing DNMT1 can promote the expression of miR-20a, thereby inhibiting the release of IL-1β and IL-18 and reducing the occurrence of cell pyroptosis. miR-20a targets negative regulation of TXNIP expression, and overexpression of TXNIP can effectively reverse the inhibitory effect of miR-20a on pyroptosis. The methylation inhibitor 5-AZ can inhibit the occurrence of pyroptosis and DR processes, while treatment with a miR-20a inhibitor or OE-TXNIP can reverse the effect of 5-AZ. DNMT1 promotes DNA methylation, decreases the expression of miR-20a and increases the expression of TXNIP, which ultimately leads to the occurrence of pyroptosis in RPE cells. •miR-20a inhibits hyperglycemia-induced pyrosis of retinal pigment epithelial cells.•DNMT1-mediated methylation is involved in the pyroptosis process of RPE cells.•DNMT1 promotes pyroptosis by mediating methylation of miR-20a.•miR-20a targets TXNIP to mediate pyroptosis in RPE cells.•DNMT1 affects the progression of diabetic retinopathy through miR-20a/TXNIP.