2003China Public HealthRequires access

Study on apoptosis induced by anthracene-9-carboxylic acid in HL-60 cells

Shisheng Zhou

Open publisher page 0 citations

Abstract

Objective To study the effects of 9-AC on apoptosis in HL-60 cells and possible intracellular factors involved in the process.Methods HL-60 cells were treated with 9-AC to induce cell apotosis.Three international accepted criteria for monitoring apoptosis were adopted,including transmission electron microscopy,agarose gel DNA electrophoresis,and fluorescence-activated cell sorter(FACS).Results 9-AC could induce apoptosis of HL-60 cells,with its concentration most optimal at 5×10 -4?mol/L.Forty-eight hours treatment of HL-60 cells with 9-AC at above concentration induced remarkable apoptotic phenomena as typified as:Ultrastructural changes formed the so-called apoptotic bodies,typical DNA ladder,symbolizing internucleosomal fragmentation of DNA were observed by using agarose gel electrophoresis of isolated DNA from HL-60 cells.FACS analysis revealed markedly apoptotic peak-subdiploid peak.Conclusion 9-AC could induce apoptosis of HL-60 cells.

About this research paper

What this paper is about

Objective To study the effects of 9-AC on apoptosis in HL-60 cells and possible intracellular factors involved in the process.Methods HL-60 cells were treated with 9-AC to induce cell apotosis.Three international accepted criteria for monitoring apoptosis were adopted,including transmission electron microscopy,agarose gel DNA electrophoresis,and fluorescence-activated cell sorter(FACS).Results 9-AC could induce apoptosis of HL-60 cells,with its concentration most optimal at 5×10 -4?mol/L.Forty-eight hours treatment of HL-60 cells with 9-AC at above concentration induced remarkable apoptotic phenomena as typified as:Ultrastructural changes formed the so-called apoptotic bodies,typical DNA ladder,symbolizing internucleosomal fragmentation of DNA were observed by using agarose gel electrophoresis of isolated DNA from HL-60 cells.FACS analysis revealed markedly apoptotic peak-subdiploid peak.Conclusion 9-AC could induce apoptosis of HL-60 cells.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To study the effects of 9-AC on apoptosis in HL-60 cells and possible intracellular factors involved in the process.Methods HL-60 cells were treated with 9-AC to induce cell apotosis.Three international accepted criteria for monitoring apoptosis were adopted,including transmission electron microscopy,agarose gel DNA electrophoresis,and fluorescence-activated cell sorter(FACS).Results 9-AC could induce apoptosis of HL-60 cells,with its concentration most optimal at 5×10 -4?mol/L.Forty-eight hours treatment of HL-60 cells with 9-AC at above concentration induced remarkable apoptotic phenomena as typified as:Ultrastructural changes formed the so-called apoptotic bodies,typical DNA ladder,symbolizing internucleosomal fragmentation of DNA were observed by using agarose gel electrophoresis of isolated DNA from HL-60 cells.FACS analysis revealed markedly apoptotic peak-subdiploid peak.Conclusion 9-AC could induce apoptosis of HL-60 cells.

Key concepts: Apoptosis, Agarose gel electrophoresis, DNA fragmentation, Molecular biology, Gel electrophoresis of nucleic acids, Gel electrophoresis, Intracellular, Chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Study on apoptosis induced by anthracene-9-carboxylic acid in HL-60 cells — Research Paper | ScholarLens