2013Chinese Journal of ArteriosclerosisRequires access

Bone Marrow Mesenchymal Stem Cells Attenuate Endothelial Cell Apoptosis Induced by ox-LDL

Shuang Wang

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Abstract

Aim To investigate whether bone marrow mesenchymal stem cells(MSC) reduce the apoptosis of human umbilical vein endothelial cells(HUVEC) induced by oxidized low density lipoprotein(ox-LDL),and related mechanisms.Methods The HUVEC were divided into three groups: HUVEC were cultured in normol medium;HUVEC were cultured with 100 mg/L ox-LDL for 24 h;and HUVEC were cocultured with MSC with 100 mg/L ox-LDL for 24 h.Then cell apoptosis of different groups were mesured by flow cytometry.The content of VEGF,as well as TNF-α,in supernatant medium were determined by ELISA,and Real-time PCR was used to detect Bcl-2 and Bax mRNA expression. Results After 24 h stimulated by ox-LDL,the HUVEC apoptosis rate was increased,and the content of VEGF,TNF-α were significantly increased,while Bcl-2 mRNA expression was downregulated and Bax mRNA upregulated.The MSC cocultured with HUVEC could increase the VEGF levels,reduce TNF-α levels,as well as increase Bcl-2 mRNA expression but reduce the expression of Bax mRNA,HUVEC apoptosis was significantly decreased.Conclusions MSC can attenuate HUVEC apoptosis induced by ox-LDL,possibly through the increase of VEGF,reduction of TNF-α,and upregulation of Bcl-2 mRNA and downregulation of Bax mRNA,which provides a theoretical basis for MSC as a treatment for endothelial injury disease such as atherosclerosis.

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Aim To investigate whether bone marrow mesenchymal stem cells(MSC) reduce the apoptosis of human umbilical vein endothelial cells(HUVEC) induced by oxidized low density lipoprotein(ox-LDL),and related mechanisms.Methods The HUVEC were divided into three groups: HUVEC were cultured in normol medium;HUVEC were cultured with 100 mg/L ox-LDL for 24 h;and HUVEC were cocultured with MSC with 100 mg/L ox-LDL for 24 h.Then cell apoptosis of different groups were mesured by flow cytometry.The content of VEGF,as well as TNF-α,in supernatant medium were determined by ELISA,and Real-time PCR was used to detect Bcl-2 and Bax mRNA expression. Results After 24 h stimulated by ox-LDL,the HUVEC apoptosis rate was increased,and the content of VEGF,TNF-α were significantly increased,while Bcl-2 mRNA expression was downregulated and Bax mRNA upregulated.The MSC cocultured with HUVEC could increase the VEGF levels,reduce TNF-α levels,as well as increase Bcl-2 mRNA expression but reduce the expression of Bax mRNA,HUVEC apoptosis was significantly decreased.Conclusions MSC can attenuate HUVEC apoptosis induced by ox-LDL,possibly through the increase of VEGF,reduction of TNF-α,and upregulation of Bcl-2 mRNA and downregulation of Bax mRNA,which provides a theoretical basis for MSC as a treatment for endothelial injury disease such as atherosclerosis.

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Available abstract

Aim To investigate whether bone marrow mesenchymal stem cells(MSC) reduce the apoptosis of human umbilical vein endothelial cells(HUVEC) induced by oxidized low density lipoprotein(ox-LDL),and related mechanisms.Methods The HUVEC were divided into three groups: HUVEC were cultured in normol medium;HUVEC were cultured with 100 mg/L ox-LDL for 24 h;and HUVEC were cocultured with MSC with 100 mg/L ox-LDL for 24 h.Then cell apoptosis of different groups were mesured by flow cytometry.The content of VEGF,as well as TNF-α,in supernatant medium were determined by ELISA,and Real-time PCR was used to detect Bcl-2 and Bax mRNA expression. Results After 24 h stimulated by ox-LDL,the HUVEC apoptosis rate was increased,and the content of VEGF,TNF-α were significantly increased,while Bcl-2 mRNA expression was downregulated and Bax mRNA upregulated.The MSC cocultured with HUVEC could increase the VEGF levels,reduce TNF-α levels,as well as increase Bcl-2 mRNA expression but reduce the expression of Bax mRNA,HUVEC apoptosis was significantly decreased.Conclusions MSC can attenuate HUVEC apoptosis induced by ox-LDL,possibly through the increase of VEGF,reduction of TNF-α,and upregulation of Bcl-2 mRNA and downregulation of Bax mRNA,which provides a theoretical basis for MSC as a treatment for endothelial injury disease such as atherosclerosis.

Key concepts: Apoptosis, Downregulation and upregulation, Umbilical vein, Mesenchymal stem cell, Flow cytometry, Bone marrow, Messenger RNA, Molecular biology

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