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Proteasome inhibitor MG132 on PC12 cell proliferation
Proteasome inhibitor MG132 on PC12 cell proliferation
Author: Cai Tong-Jian, CHEN Jing-Yuan, Li Yan, Ji Ai-ling, DU Ke-jun, LUO Wen
[Keywords:] protease inhibitor; PC12 cells; Parkinson’s disease; apoptosis
[Abstract] AIM: To investigate the effect of proteasome inhibitor MG132 on the proliferation and apoptosis of dopaminergic PC12 cells. METHODS: PC12 cells were treated with MG132 at different concentrations for 3 d. The effect of MG132 on the proliferation of PC12 cells was analyzed through MTT assay and the effect of MG132 on the apoptosis of PC12 cells was analyzed through Giemsa staining and flow cytometry. RESULTS: Treated for a same period (3 d), the inhibitory effect of MG132 on PC12 cell proliferation enhanced with the increment of the concentration of MG132 (0, 1, 2.5, 5, 10, 20 μ mol / L). The inhibitory rate exceeded 40% when the MG132 concentration was 2.5 μ mol / L, and the 50% inhibiting concentration (IC50) was 3.78 μ mol / L . MG132 also induced the apoptosis of PC12 cells obviously. The apoptosis index of the cells treated by MG132 at 2.5 μ mol / L for 3 d was 24.7% examined by Giemsa staining and 25.6% by flow cytometry, that of the control cells was 1.3% and 0% respectively. CONCLUSION: MG132 can inhibit the proliferation of dopaminergic PC12 cells and lead to apoptosis. The disfunction of proteasome may do harm to the existence of dopaminergic cells.
[Keywords] proteasome inhibitor; PC12 cells; Parkinson disease; apoptosis
[Abstract] Objective: To understand the proteasome inhibitor MG132 on PC12 dopaminergic cell proliferation and apoptosis. Methods: Using different concentrations of MG132 treatment PC12 cells, 3 d, by 3 (4,5-dimethyl-thiazol-2) 2, 5-diphenyl tetrazolium bromide salt (MTT) colorimetric detection of micro-MG132 on PC12 cell proliferation, by Giemsa staining and flow cytometry MG132 on PC12 cell apoptosis. Results: In the role of the same period of time (3 d) under the conditions, with MG132 increased the concentration of
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