2014Xiandai shengwu yixue jinzhanRequires access

TSG Up-regulate XIAP and Inhibit Apoptosis of Human Umbilical Vein Endothelial Cells

Long Shi-yi

Open publisher page 0 citations

Abstract

Objective: To investigate the effect of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) against hydrogen peroxide(H2O2) induced human umbilical vein endothelial cells(HUVECs) apoptosis and the expressions of X-linked inhibitor of apoptosis protein(XIAP), Caspase-9. Methods: HUVECs were divided into six groups: control group, H2O2group(300 μmol·L-1), TSG group(10 μmol·L-1TSG + 300 μmol·L-1H2O2), TSG and Embelin combination group(30 μmol·L-1Embelin + 10 μmol·L-1TSG + 300μmol·L-1H2O2), TSG alone treatment group(10 μmol·L-1), and Embelin group(30 μmol·L-1). The viability of HUVECs was determined with MTT as- say. Hoechst 33258 staining was used to observe the morphology of apoptosis. The mRNA expression of XIAP, Caspase-9was measured using RT-PCR. The protein expression of XIAP, Caspase-9 was detected by Western blotting. Results: Treatment HUVECs with H2O2 significantly increased the apoptosis, reduced the cell viability, decreased the expressions of XIAP and elevated Caspase-9 expression(P0.01). The expression of XIAP was inhibited by treated with Embelin alone. Compared with H2O2 group, the apoptosis rate reduced, the cell viability enhanced, the expressions of XIAP increased and Caspase-9 reduced markedly after TSG pretreated(P0.01). Combination of Embelin and TSG decreased the cell apoptosis than pretreatment of TSG, and the expression of XIAP reduced, Caspase-9 increased significantly(P0.01). Conclusion: TSG could inhibit H2O2-induced apoptosis in HUVECs, and the mechanism was associated with the expressions of XIAP and Caspase-9.

About this research paper

What this paper is about

Objective: To investigate the effect of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) against hydrogen peroxide(H2O2) induced human umbilical vein endothelial cells(HUVECs) apoptosis and the expressions of X-linked inhibitor of apoptosis protein(XIAP), Caspase-9. Methods: HUVECs were divided into six groups: control group, H2O2group(300 μmol·L-1), TSG group(10 μmol·L-1TSG + 300 μmol·L-1H2O2), TSG and Embelin combination group(30 μmol·L-1Embelin + 10 μmol·L-1TSG + 300μmol·L-1H2O2), TSG alone treatment group(10 μmol·L-1), and Embelin group(30 μmol·L-1). The viability of HUVECs was determined with MTT as- say. Hoechst 33258 staining was used to observe the morphology of apoptosis. The mRNA expression of XIAP, Caspase-9was measured using RT-PCR. The protein expression of XIAP, Caspase-9 was detected by Western blotting. Results: Treatment HUVECs with H2O2 significantly increased the apoptosis, reduced the cell viability, decreased the expressions of XIAP and elevated Caspase-9 expression(P0.01). The expression of XIAP was inhibited by treated with Embelin alone. Compared with H2O2 group, the apoptosis rate reduced, the cell viability enhanced, the expressions of XIAP increased and Caspase-9 reduced markedly after TSG pretreated(P0.01). Combination of Embelin and TSG decreased the cell apoptosis than pretreatment of TSG, and the expression of XIAP reduced, Caspase-9 increased significantly(P0.01). Conclusion: TSG could inhibit H2O2-induced apoptosis in HUVECs, and the mechanism was associated with the expressions of XIAP and Caspase-9.

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 investigate the effect of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) against hydrogen peroxide(H2O2) induced human umbilical vein endothelial cells(HUVECs) apoptosis and the expressions of X-linked inhibitor of apoptosis protein(XIAP), Caspase-9. Methods: HUVECs were divided into six groups: control group, H2O2group(300 μmol·L-1), TSG group(10 μmol·L-1TSG + 300 μmol·L-1H2O2), TSG and Embelin combination group(30 μmol·L-1Embelin + 10 μmol·L-1TSG + 300μmol·L-1H2O2), TSG alone treatment group(10 μmol·L-1), and Embelin group(30 μmol·L-1). The viability of HUVECs was determined with MTT as- say. Hoechst 33258 staining was used to observe the morphology of apoptosis. The mRNA expression of XIAP, Caspase-9was measured using RT-PCR. The protein expression of XIAP, Caspase-9 was detected by Western blotting. Results: Treatment HUVECs with H2O2 significantly increased the apoptosis, reduced the cell viability, decreased the expressions of XIAP and elevated Caspase-9 expression(P0.01). The expression of XIAP was inhibited by treated with Embelin alone. Compared with H2O2 group, the apoptosis rate reduced, the cell viability enhanced, the expressions of XIAP increased and Caspase-9 reduced markedly after TSG pretreated(P0.01). Combination of Embelin and TSG decreased the cell apoptosis than pretreatment of TSG, and the expression of XIAP reduced, Caspase-9 increased significantly(P0.01). Conclusion: TSG could inhibit H2O2-induced apoptosis in HUVECs, and the mechanism was associated with the expressions of XIAP and Caspase-9.

Key concepts: XIAP, Apoptosis, Inhibitor of apoptosis, Viability assay, Human umbilical vein endothelial cell, Umbilical vein, Chemistry, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
TSG Up-regulate XIAP and Inhibit Apoptosis of Human Umbilical Vein Endothelial Cells — Research Paper | ScholarLens