2007Shenyang Yaoke Daxue xuebaoRequires access

Simvastatin induces apoptosis in K562 cells through mitochondrial pathway

Guo-Qiang Xu

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Abstract

Objective To observe the changes of mitochondrial membrane potential(MMP),caspase-3,9 activity and cytochrome C,and determine the apoptosis signaling pathway in simvastatin-treatment K562 cells.Methods K562 cells were exposed in the 20 μmol/L simvastatin for different times(24 h,48 h,72 h).Flow cytometry were performed to confirm cell apoptotic ratio and analyze mitochondrial membrane potential;Colorimetric method was used to detect the caspase-3,9 activity;The protein of cytochrome C was detected by immunohistochemical method.Results K562 cells could undergo apoptosis after the treatment of 20 μmol/L simvastatin for 24 h,48 h and 72 h,and the apoptotic ratio are(6.1±0.35)%,(14.15±0.42)%,(30.70±0.65)%,respectively.There was a significant increase between the control groups and the text groups treated 24h.Furthermore,the percentages of MMP were(39.6±4.80)%,(24.4±2.45)%,(6.0±1.62)% at 24 h,48 h and 72 h respectively.The caspase-3,9 activity was increased compared with the control groups.The expression of cytochrome C in the 20 μmol/L simvastatin-induced K562 cell was increased.Conclusions The collapse of MMP,the up-regulated of caspase-3,9 activity and the increased cytochrome C are emerged after K562 cells treated by 20 μmol/L simvastatin.The apoptosis of K562 cells induced by simvastatin might be related to the mitochondrial pathway of apoptosis.

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Objective To observe the changes of mitochondrial membrane potential(MMP),caspase-3,9 activity and cytochrome C,and determine the apoptosis signaling pathway in simvastatin-treatment K562 cells.Methods K562 cells were exposed in the 20 μmol/L simvastatin for different times(24 h,48 h,72 h).Flow cytometry were performed to confirm cell apoptotic ratio and analyze mitochondrial membrane potential;Colorimetric method was used to detect the caspase-3,9 activity;The protein of cytochrome C was detected by immunohistochemical method.Results K562 cells could undergo apoptosis after the treatment of 20 μmol/L simvastatin for 24 h,48 h and 72 h,and the apoptotic ratio are(6.1±0.35)%,(14.15±0.42)%,(30.70±0.65)%,respectively.There was a significant increase between the control groups and the text groups treated 24h.Furthermore,the percentages of MMP were(39.6±4.80)%,(24.4±2.45)%,(6.0±1.62)% at 24 h,48 h and 72 h respectively.The caspase-3,9 activity was increased compared with the control groups.The expression of cytochrome C in the 20 μmol/L simvastatin-induced K562 cell was increased.Conclusions The collapse of MMP,the up-regulated of caspase-3,9 activity and the increased cytochrome C are emerged after K562 cells treated by 20 μmol/L simvastatin.The apoptosis of K562 cells induced by simvastatin might be related to the mitochondrial pathway of apoptosis.

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Available abstract

Objective To observe the changes of mitochondrial membrane potential(MMP),caspase-3,9 activity and cytochrome C,and determine the apoptosis signaling pathway in simvastatin-treatment K562 cells.Methods K562 cells were exposed in the 20 μmol/L simvastatin for different times(24 h,48 h,72 h).Flow cytometry were performed to confirm cell apoptotic ratio and analyze mitochondrial membrane potential;Colorimetric method was used to detect the caspase-3,9 activity;The protein of cytochrome C was detected by immunohistochemical method.Results K562 cells could undergo apoptosis after the treatment of 20 μmol/L simvastatin for 24 h,48 h and 72 h,and the apoptotic ratio are(6.1±0.35)%,(14.15±0.42)%,(30.70±0.65)%,respectively.There was a significant increase between the control groups and the text groups treated 24h.Furthermore,the percentages of MMP were(39.6±4.80)%,(24.4±2.45)%,(6.0±1.62)% at 24 h,48 h and 72 h respectively.The caspase-3,9 activity was increased compared with the control groups.The expression of cytochrome C in the 20 μmol/L simvastatin-induced K562 cell was increased.Conclusions The collapse of MMP,the up-regulated of caspase-3,9 activity and the increased cytochrome C are emerged after K562 cells treated by 20 μmol/L simvastatin.The apoptosis of K562 cells induced by simvastatin might be related to the mitochondrial pathway of apoptosis.

Key concepts: Simvastatin, Apoptosis, Cytochrome c, K562 cells, Flow cytometry, Molecular biology, Chemistry, Mitochondrion

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