2008Huazhong Normal University Journal of PostgraduatesRequires access

Influence of CSA on Apoptosis Induced by SfaMNPV In SL-1 Cells

Suying Guo

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Abstract

To investigate the effects of mitochondrial membrane permeability transition pore MPT-closed agent CSA on SfaMNPV induced apoptosis in SL-1 cell line. SL-1 cells were treated with SfaMNPV alone or in combination with CSA in different concentrations. Cell apoptosis was assessed by the morphological observation , DNA electrophoresis and flow cytometry. The mitochondrial transmembrane potentials (ΔΨm) were detected by flow cytometry according to the intensity of rhodamine 123 uptake in cells. CSA prevented SL-1 cells treated by SfaMNPV from apoptosis. CSA significantly restrained mitochondrial membrane potential of apoptotic SL-1 cells from degression. CSA restraining ΔΨm from degression possibly involves with CSA binding to CyP-D and CSA prevented SL-1 cells from apoptosis.

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What this paper is about

To investigate the effects of mitochondrial membrane permeability transition pore MPT-closed agent CSA on SfaMNPV induced apoptosis in SL-1 cell line. SL-1 cells were treated with SfaMNPV alone or in combination with CSA in different concentrations. Cell apoptosis was assessed by the morphological observation , DNA electrophoresis and flow cytometry. The mitochondrial transmembrane potentials (ΔΨm) were detected by flow cytometry according to the intensity of rhodamine 123 uptake in cells. CSA prevented SL-1 cells treated by SfaMNPV from apoptosis. CSA significantly restrained mitochondrial membrane potential of apoptotic SL-1 cells from degression. CSA restraining ΔΨm from degression possibly involves with CSA binding to CyP-D and CSA prevented SL-1 cells from apoptosis.

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Available abstract

To investigate the effects of mitochondrial membrane permeability transition pore MPT-closed agent CSA on SfaMNPV induced apoptosis in SL-1 cell line. SL-1 cells were treated with SfaMNPV alone or in combination with CSA in different concentrations. Cell apoptosis was assessed by the morphological observation , DNA electrophoresis and flow cytometry. The mitochondrial transmembrane potentials (ΔΨm) were detected by flow cytometry according to the intensity of rhodamine 123 uptake in cells. CSA prevented SL-1 cells treated by SfaMNPV from apoptosis. CSA significantly restrained mitochondrial membrane potential of apoptotic SL-1 cells from degression. CSA restraining ΔΨm from degression possibly involves with CSA binding to CyP-D and CSA prevented SL-1 cells from apoptosis.

Key concepts: Rhodamine 123, Apoptosis, Flow cytometry, Membrane potential, Mitochondrial permeability transition pore, Molecular biology, Cell biology, Chemistry

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