2008Journal of Harbin University of CommerceRequires access

Effect of juglone in Qinglongyi on cell cycle status and apoptosis in A-549 cells

JI Yu-bin

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Abstract

To explore the inhibition of juglone in Qinglongyi on A-549 cells in vitro,MTT assay is used.Laser confocal scanning microscope is used to observe apoptotic morphology.Changes of cell cycle are studied by flow cytometry analysis.The result of MTT assay showed that juglone had a marked growth inhibition in A-549 cells and the IC50 is respectively 3.4×10-5mol/L,1.8×10-5mol/L and 2.6×10-6mol/L after treatment for 24,48 and 72 h by juglone.Through laser confocal scanning microscope,it can be concluded that juglone can induce the apoptosis.Cell cycle changes are analyzed by flow cytometry with cells at G1 phase significantly less than those of control and cells at G2 phase significantly more than those of control.The result suggests that juglone could apoptosis of A-549 cells with the cell cycle arrest on G2 and S phase in distinct dose-dependent manner.

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What this paper is about

To explore the inhibition of juglone in Qinglongyi on A-549 cells in vitro,MTT assay is used.Laser confocal scanning microscope is used to observe apoptotic morphology.Changes of cell cycle are studied by flow cytometry analysis.The result of MTT assay showed that juglone had a marked growth inhibition in A-549 cells and the IC50 is respectively 3.4×10-5mol/L,1.8×10-5mol/L and 2.6×10-6mol/L after treatment for 24,48 and 72 h by juglone.Through laser confocal scanning microscope,it can be concluded that juglone can induce the apoptosis.Cell cycle changes are analyzed by flow cytometry with cells at G1 phase significantly less than those of control and cells at G2 phase significantly more than those of control.The result suggests that juglone could apoptosis of A-549 cells with the cell cycle arrest on G2 and S phase in distinct dose-dependent manner.

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Available abstract

To explore the inhibition of juglone in Qinglongyi on A-549 cells in vitro,MTT assay is used.Laser confocal scanning microscope is used to observe apoptotic morphology.Changes of cell cycle are studied by flow cytometry analysis.The result of MTT assay showed that juglone had a marked growth inhibition in A-549 cells and the IC50 is respectively 3.4×10-5mol/L,1.8×10-5mol/L and 2.6×10-6mol/L after treatment for 24,48 and 72 h by juglone.Through laser confocal scanning microscope,it can be concluded that juglone can induce the apoptosis.Cell cycle changes are analyzed by flow cytometry with cells at G1 phase significantly less than those of control and cells at G2 phase significantly more than those of control.The result suggests that juglone could apoptosis of A-549 cells with the cell cycle arrest on G2 and S phase in distinct dose-dependent manner.

Key concepts: Juglone, Flow cytometry, Apoptosis, Cell cycle, MTT assay, Confocal, Molecular biology, Confocal microscopy

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