Diosgenin improves lipid metabolism in diabetic nephropathy via regulation of miR-148b-3p/DNMT1/FOXO1 axis.

IF 2.3 4区 医学 Q2 UROLOGY & NEPHROLOGY
Nephron Pub Date : 2024-11-27 DOI:10.1159/000541690
Min Luo, Zongren Hu, Jichang Yang, Jinhan Yang, Wen Sheng, Chengxiong Lin, Dian Li, Qinghu He
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引用次数: 0

Abstract

Background: The progression of diabetic nephropathy (DN) is closely associated with lipid accumulation. Diosgenin (Dio) plays a beneficial role in the lipid metabolism associated with multiple diseases. Thus, the mechanism underlying Dio's function in DN associated with aberrant lipid accumulation warrants further investigation.

Methods: To model DN in vitro, HK-2 cells were treated with high glucose (HG) and palmitic acid. Cell viability was evaluated using MTT assay. The triglyceride (TG) content in HK-2 cells was measured using a commercial assay kit. The formation of lipid droplets in HK-2 cells was observed using Oil Red O staining. The expression levels of mRNA and protein were detected using RT-qPCR and western blot, respectively. The DNA methylation of FOXO1 was assessed using MSP. The interaction between DNMT1 and the FOXO1 promoter was confirmed by ChIP assay.

Results: Dio treatment reduced TG levels and lipid droplet formation in HK-2 cells co-treated with HG and palmitic acid. Simultaneously, the levels of miR-148b-3p and FOXO1 were increased by Dio, while Dio decreased the expression levels of DNMT1 and SREBP-2. Meanwhile, miR-148b-3p can bind to DNMT1, which in turn inhibits the expression of FOXO1 by mediating the DNA methylation of FOXO1. In addition, FOXO1 negatively regulates the expression of SREBP-2 by interacting with the SREBP-2 promoter. MiR-148b-3p inhibition or silencing of FOXO1 abolished the inhibitory effect of Dio on TG production and lipid droplet formation. This effect was further exacerbated by the downregulation of DNMT1. FOXO1 overexpression may counteract the promotive effects of miR-148b-3p inhibitor on lipid accumulation.

Conclusion: Dio treatment reduced TG production and lipid droplet formation in HK-2 cells during the progression of DN by modulating the miR-148b-3p/DNMT1/FOXO1/SREBP-2 axis. This finding provides new evidence supporting the therapeutic potential of Dio for DN.

薯蓣皂苷通过调节 miR-148b-3p/DNMT1/FOXO1 轴改善糖尿病肾病的脂质代谢
背景:糖尿病肾病(DN)的进展与脂质积累密切相关。薯蓣皂苷(Dio)在与多种疾病相关的脂质代谢中发挥着有益的作用。因此,Dio 在与脂质异常积累相关的 DN 中发挥作用的机制值得进一步研究:方法:为了在体外模拟 DN,用高糖(HG)和棕榈酸处理 HK-2 细胞。用 MTT 法评估细胞活力。HK-2 细胞中的甘油三酯 (TG) 含量使用商业检测试剂盒进行测量。用油红 O 染色法观察 HK-2 细胞中脂滴的形成。利用 RT-qPCR 和 Western 印迹分别检测了 mRNA 和蛋白质的表达水平。使用 MSP 评估了 FOXO1 的 DNA 甲基化情况。通过 ChIP 检测证实了 DNMT1 与 FOXO1 启动子之间的相互作用:结果:Dio处理可降低HG和棕榈酸联合处理的HK-2细胞中的TG水平和脂滴的形成。同时,Dio 提高了 miR-148b-3p 和 FOXO1 的水平,而 DNMT1 和 SREBP-2 的表达水平则有所下降。同时,miR-148b-3p 能与 DNMT1 结合,而 DNMT1 又能通过介导 FOXO1 的 DNA 甲基化来抑制 FOXO1 的表达。此外,FOXO1 通过与 SREBP-2 启动子相互作用,对 SREBP-2 的表达进行负向调节。抑制 MiR-148b-3p 或沉默 FOXO1 可消除 Dio 对 TG 生成和脂滴形成的抑制作用。DNMT1 的下调进一步加剧了这种效应。FOXO1的过表达可能会抵消miR-148b-3p抑制剂对脂质积累的促进作用:结论:Dio通过调节miR-148b-3p/DNMT1/FOXO1/SREBP-2轴,在DN进展过程中减少了HK-2细胞中TG的产生和脂滴的形成。这一发现为 Dio 治疗 DN 的潜力提供了新的证据。
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来源期刊
Nephron
Nephron UROLOGY & NEPHROLOGY-
CiteScore
5.00
自引率
0.00%
发文量
80
期刊介绍: ''Nephron'' comprises three sections, which are each under the editorship of internationally recognized leaders and served by specialized Associate Editors. Apart from high-quality original research, ''Nephron'' publishes invited reviews/minireviews on up-to-date topics. Papers undergo an innovative and transparent peer review process encompassing a Presentation Report which assesses and summarizes the presentation of the paper in an unbiased and standardized way.
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