Effects of β amyloid peptide 25-35 on the expression of p53 and bcl-2 genes in cells of PC12 cell line
Qifeng Zhu
Abstract
Qifeng Zhu
Abstract
Objective: To observe the phenomenon of apoptosis and the change of the expression of p53 and bcl-2 genes induced by β amyloid peptide 25-35 (Aβ 25-35 ) in PC12 cell line. Methods: After the treatment of PC12 cells with different concentrations of Aβ 25-35 (0, 5, 10, 20 μmol/L)for 24h,the MTT assay was used to evaluate the cell survival rate, the Hoechst-PI fluorescence staining and DNA Ladder-agarose gel electrophoresis were used to observe the apoptosis status, and the RT-PCR and western blot were used to detect the expression of p53 and bcl-2 genes at mRNA and protein levels, respectively. Results: In a dose-dependent manner from the low dosage to the high dosage, Aβ 25-35 reduced the survival rate of PC12 cells, induced apoptosis, increased the mRNA and protein levels of p53 gene, and decrease the mRNA and protein levels of bcl-2 gene. Conclusion: Aβ 25-35 might induce the apoptosis of PC12 cells by up-regulating the expression of p53 gene and down-regulating the expression of bcl-2 gene.
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 observe the phenomenon of apoptosis and the change of the expression of p53 and bcl-2 genes induced by β amyloid peptide 25-35 (Aβ 25-35 ) in PC12 cell line. Methods: After the treatment of PC12 cells with different concentrations of Aβ 25-35 (0, 5, 10, 20 μmol/L)for 24h,the MTT assay was used to evaluate the cell survival rate, the Hoechst-PI fluorescence staining and DNA Ladder-agarose gel electrophoresis were used to observe the apoptosis status, and the RT-PCR and western blot were used to detect the expression of p53 and bcl-2 genes at mRNA and protein levels, respectively. Results: In a dose-dependent manner from the low dosage to the high dosage, Aβ 25-35 reduced the survival rate of PC12 cells, induced apoptosis, increased the mRNA and protein levels of p53 gene, and decrease the mRNA and protein levels of bcl-2 gene. Conclusion: Aβ 25-35 might induce the apoptosis of PC12 cells by up-regulating the expression of p53 gene and down-regulating the expression of bcl-2 gene.
Key concepts: Apoptosis, Molecular biology, Agarose gel electrophoresis, Gene, Gene expression, Messenger RNA, Western blot, Cell culture