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Oxid Med Cell Longev ; 2019: 1076512, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31827667

RESUMO

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.


Assuntos
Biflavonoides/farmacologia , Catequina/farmacologia , MicroRNAs/metabolismo , Proantocianidinas/farmacologia , Regulação para Cima/efeitos dos fármacos , Vitis/química , Regiões 3' não Traduzidas , Animais , Apoptose/efeitos dos fármacos , Sequência de Bases , Sobrevivência Celular/efeitos dos fármacos , Feminino , Células da Granulosa/citologia , Células da Granulosa/metabolismo , Extrato de Sementes de Uva/química , Peróxido de Hidrogênio/farmacologia , Ovário/citologia , Estresse Oxidativo/efeitos dos fármacos , Espécies Reativas de Oxigênio/metabolismo , Alinhamento de Sequência , Suínos , Vitis/metabolismo , Receptor fas/química , Receptor fas/genética , Receptor fas/metabolismo
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