KMID : 1141520220370060901
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Endocrinology and Metabolism 2022 Volume.37 No. 6 p.901 ~ p.917
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Inhibition of miR-146a-5p and miR-8114 in Insulin-Secreting Cells Contributes to the Protection of Melatonin against Stearic Acid-Induced Cellular Senescence by Targeting Mafa
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Su Shenghan
Zhao Qingrui Dan Lingfeng Lin Yuqing Li Xuebei Zhang Yunjin Yang Chunxiao Dong Yimeng Li Xiaohan Regazzi Romano Sun Changhao Chu Xia Lu Huimin
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Abstract
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Background: Chronic exposure to elevated levels of saturated fatty acids results in pancreatic ¥â-cell senescence. However, targets and effective agents for preventing stearic acid-induced ¥â-cell senescence are still lacking. Although melatonin administration can protect ¥â-cells against lipotoxicity through anti-senescence processes, the precise underlying mechanisms still need to be explored. Therefore, we investigated the anti-senescence effect of melatonin on stearic acid-treated mouse ¥â-cells and elucidated the possible role of microRNAs in this process.
Methods: ¥â-Cell senescence was identified by measuring the expression of senescence-related genes and senescence-associated ¥â-galactosidase staining. Gain- and loss-of-function approaches were used to investigate the involvement of microRNAs in stearic acid-evoked ¥â-cell senescence and dysfunction. Bioinformatics analyses and luciferase reporter activity assays were applied to predict the direct targets of microRNAs.
Results: Long-term exposure to a high concentration of stearic acid-induced senescence and upregulated miR-146a-5p and miR-8114 expression in both mouse islets and ¥â-TC6 cell lines. Melatonin effectively suppressed this process and reduced the levels of these two miRNAs. A remarkable reversibility of stearic acid-induced ¥â-cell senescence and dysfunction was observed after silencing miR-146a-5p and miR-8114. Moreover, V-maf musculoaponeurotic fibrosarcoma oncogene homolog A (Mafa) was verified as a direct target of miR-146a-5p and miR-8114. Melatonin also significantly ameliorated senescence and dysfunction in miR-146a-5pand miR-8114-transfected ¥â-cells.
Conclusion: These data demonstrate that melatonin protects against stearic acid-induced ¥â-cell senescence by inhibiting miR-146a- 5p and miR-8114 and upregulating Mafa expression. This not only provides novel targets for preventing stearic acid-induced ¥â-cell dysfunction, but also points to melatonin as a promising drug to combat type 2 diabetes progression.
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KEYWORD
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Stearic acid, Melatonin, MicroRNAs, Cellular senescence, Mafa
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