miR-34aregulates high glucose-induced apoptosis of H9c2cells
Fan Zhao
Abstract
Fan Zhao
Abstract
Objective To study the effect of miR-34aon regulation of high glucose-induced apoptosis of H9c2cells.Methods Cultured H9c2cells were randomly divided into normal glucose(5.5mmol/L)group,high glucose(33mmol/L)group and miR-34ainhibitor(50nmol/L)+glucose(33mmol/L)group.Expressions of miR-34aand Bcl-2mRNA were detected by RT-PCR.Western blot was used to monitor the changes in apopotosis-associated protein Bcl-2,respectively.Apoptosis of-H9c2cells was detected by flow cytometry.Results The apoptpsis level of H9c2cells and the expression level of miR-34ain H9c2cells were significantly higher whereas the expression level of Bcl-2was significantly lower in high glucose group than in normal glucose group(P0.05).The apoptpsis level of H9c2cells was significantly lower whereas the expression level of Bcl-2was significantly higher in miR-34ainhibitor+glucose group than in high glucose group(P0.05).Conclusion miR-34aregulates high glucose-induced apoptpsis of H9c2cells by inhibiting the expression of Bcl-2.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To study the effect of miR-34aon regulation of high glucose-induced apoptosis of H9c2cells.Methods Cultured H9c2cells were randomly divided into normal glucose(5.5mmol/L)group,high glucose(33mmol/L)group and miR-34ainhibitor(50nmol/L)+glucose(33mmol/L)group.Expressions of miR-34aand Bcl-2mRNA were detected by RT-PCR.Western blot was used to monitor the changes in apopotosis-associated protein Bcl-2,respectively.Apoptosis of-H9c2cells was detected by flow cytometry.Results The apoptpsis level of H9c2cells and the expression level of miR-34ain H9c2cells were significantly higher whereas the expression level of Bcl-2was significantly lower in high glucose group than in normal glucose group(P0.05).The apoptpsis level of H9c2cells was significantly lower whereas the expression level of Bcl-2was significantly higher in miR-34ainhibitor+glucose group than in high glucose group(P0.05).Conclusion miR-34aregulates high glucose-induced apoptpsis of H9c2cells by inhibiting the expression of Bcl-2.
Key concepts: Apoptosis, Flow cytometry, Western blot, Endocrinology, Medicine, Internal medicine, Andrology, Molecular biology