Effects of MPP~+ on proliferation and ERK activation of PC12 cells
Wen Luo
Abstract
Wen Luo
Abstract
Objective To study the toxicity of 1-methy1-4-phenylpyridinium ion(MPP+)on rat pheochromocytoma PC12 cells in vitro.Methods PC12 cell cultures were exposed to 100,300,500 μmol/L MPP+.The inhibition of the cell proliferation was determined by MTT assay.Western blot was performed to determine the level of phosphorylated extracellular signal-regulated protein kinase(ERK).Results MPP+ exposure inhibited the proliferation of PC12 cells in a dose-and time-dependent manner.The inhibitory rates were 17.86%-58.06%.Western-blot showed that MPP+ decreased the phosphorylation of ERK1/2(P0.01).PD98059,a selective inhibitor of MEK,further inhibited the proliferation of PC12 cells.Conclusion MPP+ can significantly inhibit the proliferation of PC12 cells.The reduction of ERK1/2 phosphorylation could be an important molecular mechanism of MPP+-induced dopaminergic neurotoxicity.
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 toxicity of 1-methy1-4-phenylpyridinium ion(MPP+)on rat pheochromocytoma PC12 cells in vitro.Methods PC12 cell cultures were exposed to 100,300,500 μmol/L MPP+.The inhibition of the cell proliferation was determined by MTT assay.Western blot was performed to determine the level of phosphorylated extracellular signal-regulated protein kinase(ERK).Results MPP+ exposure inhibited the proliferation of PC12 cells in a dose-and time-dependent manner.The inhibitory rates were 17.86%-58.06%.Western-blot showed that MPP+ decreased the phosphorylation of ERK1/2(P0.01).PD98059,a selective inhibitor of MEK,further inhibited the proliferation of PC12 cells.Conclusion MPP+ can significantly inhibit the proliferation of PC12 cells.The reduction of ERK1/2 phosphorylation could be an important molecular mechanism of MPP+-induced dopaminergic neurotoxicity.
Key concepts: MAPK/ERK pathway, Western blot, Phosphorylation, Cell growth, Kinase, Chemistry, Cell biology, Molecular biology