Grape Seed Procyanidin B2 Protects Porcine Ovarian Granulosa Cells against Oxidative Stress-Induced Apoptosis by Upregulating let-7a Expression.
Jia Qing ZhangXian-Wei WangJun-Feng ChenQiao-Ling RenJing WangBin-Wen GaoZhi-Hai ShiZi-Jing ZhangXian-Xiao BaiBao-Song XingPublished in: Oxidative medicine and cellular longevity (2019)
Oxidative stress is a causal factor and key promoter of all kinds of reproductive disorders related to granulosa cell (GC) apoptosis that acts by dysregulating the expression of related genes. Various studies have suggested that grape seed procyanidin B2 (GSPB2) may protect GCs from oxidative injury, though the underlying mechanisms are not fully understood. Therefore, whether the beneficial effects of GSPB2 are associated with microRNAs, which have been suggested to play a critical role in GC apoptosis by regulating the expression of protein-coding genes, was investigated in this study. The results showed that GSPB2 treatment protected GCs from a H2O2-induced apoptosis, as detected by an MTT assay and TUNEL staining, and increased let-7a expression in GCs. Furthermore, let-7a overexpression markedly increased cell viability and inhibited H2O2-induced GC apoptosis. Furthermore, the overexpression of let-7a reduced the upregulation of Fas expression in H2O2-treated GCs at the mRNA and protein levels. Dual-luciferase reporter assay results indicated that let-7a directly targets the Fas 3'-UTR. Furthermore, the overexpression of let-7a enhanced the protective effects of GSPB2 against GC apoptosis induced by H2O2. These results indicate that GSPB2 inhibits H2O2-induced apoptosis of GCs, possibly through the upregulation of let-7a.
Keyphrases
- induced apoptosis
- oxidative stress
- endoplasmic reticulum stress
- poor prognosis
- signaling pathway
- diabetic rats
- binding protein
- cell cycle arrest
- dna damage
- cell proliferation
- long non coding rna
- ischemia reperfusion injury
- gene expression
- crispr cas
- dna methylation
- polycystic ovary syndrome
- mass spectrometry
- type diabetes
- skeletal muscle
- metabolic syndrome
- genome wide
- heat shock
- stress induced
- simultaneous determination
- newly diagnosed
- atomic force microscopy