Picroside â
¡ alleviates renal fibrosis through YY1-dependent transcriptional inhibition of TGFß1.
Metabol Open
; 23: 100316, 2024 Sep.
Article
in En
| MEDLINE
| ID: mdl-39286296
ABSTRACT
Diabetic Nephropathy (DN) has become the leading cause of end-stage renal disease worldwide. Studies have indicated that Transforming Growth Factor beta1 (TGFß1) is the most potent factor contributing to renal fibrosis, and understanding the exact pathogenic mechanism of renal fibrosis is crucial for alleviating the condition. Previous research has identified Yin Yang 1 (YY1) as an effective inhibitor of TGF-ß1. Our study, through dual-luciferase reporter gene assays and Western blot experiments, screened and obtained the small molecule compound Pdâ
¡. Subsequently, validation in a high-glucose-induced renal mesangial cell injury model showed that Pdâ
¡ treatment significantly increased the expression of YY1 protein and mRNA, while correspondingly reducing the expression of TGFß1 protein and mRNA. Dual-luciferase reporter gene assay results revealed that, compared to the control group, the luciferase transcription activity of YY1 molecules increased in the Pdâ
¡ treatment group, and the luciferase transcription activity of TGFß1 decreased. By further designing mutations in the binding sites between TGFß1 and YY1 on the promoter, transfecting fluorescent enzyme reporter gene plasmids with TGFß1 mutant promoter into mesangial cells damaged by high glucose, and then treating the cells with Pdâ
¡, it was observed that the luciferase transcription activity of TGFß1 did not decrease. Therefore, these results suggest that Pdâ
¡ may inhibit TGFß1 transcriptional activity by activating YY1, thereby slowing down the progression of diabetic nephropathy.
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01-internacional
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MEDLINE
Language:
En
Journal:
Metabol Open
Year:
2024
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Article
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