Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

ATORVASTATIN DELAY THE SENESCENCE OF VASCULAR ENDOTHELIAL CELL INDUCED BY ANGIOTENSINII THROUGH REGULATING THE EXPRESSION OF BCL-2/BAX PROTEIN

View through CrossRef
Objectives To explore the effects of Atorvastatin on the senescence in human umbilical vein endothelial cells (HUVECs) induced by AngiotensinII (AngII) and to study its potential molecular mechanism. Methods The HUVECs were cultured in vitro and divided into three groups, the control group, AngII group (stimulated with intervened by AngII 10–6 mol/l for 48 h), Atorvastatin group (10-3 mol/l Atorvastatin was added to cell 1 h before 10-6 mol/l AngII). B-Gal stain and cell cycle analysis were used to identify cell aging status; and the expression of apoptosis-association genes Bcl-2 and Bax were detected by immunocytochemistry, and western-blot. Results AngII stimulation enhanced the positive cell number of B-gal stained HUVECs, depressed cell proliferation. The AngII group inhibited the expression of Bcl-2 protein expression and increased the expression of Bax protein expression compared with the Atorvastatin group markedly p<0.05), Bcl-2/Bax was decreased significantly p<0.05) in the AngII group. The Atorvastatin group increased the expression of Bcl-2 protein expression and decreased the expression of Bax protein expression compared with the AngII group evidently p<0.05), Bcl-2/Bax was increased significantly p<0.05) in the Atorvastatin group. Conclusions Atorvastatin probably delay the senescence of vascular endothelial cell induced by AngII through regulating the expression of Bcl-2/Bax protein.
Title: ATORVASTATIN DELAY THE SENESCENCE OF VASCULAR ENDOTHELIAL CELL INDUCED BY ANGIOTENSINII THROUGH REGULATING THE EXPRESSION OF BCL-2/BAX PROTEIN
Description:
Objectives To explore the effects of Atorvastatin on the senescence in human umbilical vein endothelial cells (HUVECs) induced by AngiotensinII (AngII) and to study its potential molecular mechanism.
Methods The HUVECs were cultured in vitro and divided into three groups, the control group, AngII group (stimulated with intervened by AngII 10–6 mol/l for 48 h), Atorvastatin group (10-3 mol/l Atorvastatin was added to cell 1 h before 10-6 mol/l AngII).
B-Gal stain and cell cycle analysis were used to identify cell aging status; and the expression of apoptosis-association genes Bcl-2 and Bax were detected by immunocytochemistry, and western-blot.
Results AngII stimulation enhanced the positive cell number of B-gal stained HUVECs, depressed cell proliferation.
The AngII group inhibited the expression of Bcl-2 protein expression and increased the expression of Bax protein expression compared with the Atorvastatin group markedly p<0.
05), Bcl-2/Bax was decreased significantly p<0.
05) in the AngII group.
The Atorvastatin group increased the expression of Bcl-2 protein expression and decreased the expression of Bax protein expression compared with the AngII group evidently p<0.
05), Bcl-2/Bax was increased significantly p<0.
05) in the Atorvastatin group.
Conclusions Atorvastatin probably delay the senescence of vascular endothelial cell induced by AngII through regulating the expression of Bcl-2/Bax protein.

Related Results

GW24-e2958 Atrovastatin delay the senescence of vascular endothelial
GW24-e2958 Atrovastatin delay the senescence of vascular endothelial
Objectives To explore the effects of Atorvastatin on the senescence in human umbilical vein endothelial cells (HUVECs) induced by AngiotensinII (AngII) and to stu...
Study of the regulatory mechanism involved in dark-induced Postharvest leaf senescence
Study of the regulatory mechanism involved in dark-induced Postharvest leaf senescence
Postharvest leaf senescence contributes to quality losses in flowers and leafy vegetables. The general goal of this research project was to investigate the regulatory mechanisms in...
Characterization of the anti-apoptotic mechanism of Bcl-B
Characterization of the anti-apoptotic mechanism of Bcl-B
Bcl-B protein is an anti-apoptotic member of the Bcl-2 family protein that contains all the four BH (Bcl-2 homology) domains (BH1, BH2, BH3 and BH4) and a predicted C-terminal tran...
Abstract A16: Wnt antagonist SFRP1 functions as secreted mediator of senescence
Abstract A16: Wnt antagonist SFRP1 functions as secreted mediator of senescence
Abstract The purpose of this study was 1) to identify the mediator(s) of senescence that are secreted from senescent cells and induce senescence in an autocrine and ...
EFFECT OF ERK1/2 SIGNAL TRANSDUCTION PATHWAY IN VASCULAR ENDOTHELIAL CELL APOPTOSIS
EFFECT OF ERK1/2 SIGNAL TRANSDUCTION PATHWAY IN VASCULAR ENDOTHELIAL CELL APOPTOSIS
Objectives To explore the changes in extracellar signal-regulated protein kinase (ERK1/2) in endothelial cell senescence induced by AngiotensinII at the different...
Dissection of functional domains in Bcl-2α by site-directed mutagenesis
Dissection of functional domains in Bcl-2α by site-directed mutagenesis
Bcl-2α is a mitochondrial or perinuclear-associated oncoprotein that prolongs the life span of a variety of cell types by interfering with programmed cell death. How Bcl-2 confers ...
7 th International Symposium on Enabling Technologies for Life Sciences (ETP)
7 th International Symposium on Enabling Technologies for Life Sciences (ETP)
The seventh in the series of ETP Symposia (see Rapid Communications in Mass Spectrometry 2012, 26 , ...
Abstract 1583: Bcl-6 as a potential therapeutic target for bladder cancer
Abstract 1583: Bcl-6 as a potential therapeutic target for bladder cancer
Abstract Introduction and Objectives: B-cell lymphoma 6 (Bcl-6) is known to be a nuclear protein and a master transcription factor for regulation of T follicular hel...

Back to Top