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Dexamethasone-induced apoptosis of murine MIN6 pancreatic β-cells and its effect on AKT phosphorylation

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Author:
No author available
Journal Title:
ACTA PHARMACEUTICA SINICA
Issue:
11
DOI:
10.3321/j.issn:0513-4870.2009.11.005
Key Word:
地塞米松;胰岛β细胞;细胞凋亡;Bcl-2;Bax;AKT;dexamethasone;pancreatic β-cell;apoptosis;Bcl-2;Bax;AKT

Abstract: This study is to investigate the effect of dexamethasone on cell apoptosis of murine MIN6 pancreatic β-cells, and to investigate the mechanism of dexamethasone-dependent cell apoptosis. The cell apoptosis model was established by choosing the murine MIN6 pancreatic β-cells, which was cultured in vitro and induced by dexamethasone. The morphology of the cell apoptosis was observed through fluorescence microscopic analysis after Hochest/PI staining and flow cytometric assay after Annexin-V/PI staining. The expression of caspase-3 was detected with caspase-3 activity assay kit. The expressions of Cyt-c, Bcl-2, Bax, AKT and p-AKT were observed with Western blotting. The results indicated that after exposure to dexamethasone at a concentration ranging from 50-800 nmol·L~(-1) for 48 h, the percentage of cell apoptosis was significantly increased with the concentration over 100 nmol·L~(-1) of dexamethasone; after exposure to dexamethasone (100 nmol·L~(-1)) for 72 h, the activity of caspase-3 increased significantly; after exposure to dexamethasone at a concentration ranging from 50-800 nmol·L~(-1) for 48 h, the expression of Cyt-c increased, Bcl-2 and AKT phosphorylation decreased while Bax and T-AKT remained unchanged. It could be concluded that the effect of dexamethasone on murine MIN6 pancreatic β-cells apoptosis is significant. The mechanism of dexamethasone-dependent cell apoptosis is probably related to down regulation of the Bcl-2 expression and reduction of AKT phosphorylation.

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