The Experimental Studies of Apoptosis Induced by MPP~+ in PC12 Cells
Fang Liu
Abstract
Fang Liu
Abstract
By the techniques cell cultivation outside body, MTT assay, Fluorescence Staining, Transmission Electron Microscopy, and Flow Cytometry, we studied the effects of MPP~+ on proliferation and apoptosis in PC12 cells to provide experimental model for the study of neuroprotective effect. Result indicates that MPP~+ can induce apoptosis in PC12 cells, which showed the dependence on time and concentration. When PC12 cells were treated with 0.20 mM MPP~+ for 48 hours, cell viability was reduced to about 60% as determined by MTT assay, cell nuclear was agglomerated and ruptured, series changes was occurred in ultrastructure. All above results showed distinctive apoptosis characters.Annexin V-FITC apoptosis double-stained kit with Flow Cytometry shows that the visible cells were about 20.2%, late apoptosis/necrosis cells were about 51% and early apoptotic cells were about 6.75% It suggests that MPP~+ can induce apoptosis in PC12 cells, which is a valuable experimental model for the study of neuroprotective effect.
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By the techniques cell cultivation outside body, MTT assay, Fluorescence Staining, Transmission Electron Microscopy, and Flow Cytometry, we studied the effects of MPP~+ on proliferation and apoptosis in PC12 cells to provide experimental model for the study of neuroprotective effect. Result indicates that MPP~+ can induce apoptosis in PC12 cells, which showed the dependence on time and concentration. When PC12 cells were treated with 0.20 mM MPP~+ for 48 hours, cell viability was reduced to about 60% as determined by MTT assay, cell nuclear was agglomerated and ruptured, series changes was occurred in ultrastructure. All above results showed distinctive apoptosis characters.Annexin V-FITC apoptosis double-stained kit with Flow Cytometry shows that the visible cells were about 20.2%, late apoptosis/necrosis cells were about 51% and early apoptotic cells were about 6.75% It suggests that MPP~+ can induce apoptosis in PC12 cells, which is a valuable experimental model for the study of neuroprotective effect.
Key concepts: Apoptosis, Flow cytometry, Annexin, MTT assay, Viability assay, Neuroprotection, Molecular biology, Staining