RETRACTED: Astragaloside IV inhibits platelet-derived growth factor-BB-stimulated proliferation and migration of vascular smooth muscle cells via the inhibition of p38 MAPK signaling (Retracted Article)

被引:45
作者
Chen, Zhuo [1 ]
Cai, Ying [1 ]
Zhang, Wenliang [1 ]
Liu, Xinzhou [1 ]
Liu, Suixin [1 ]
机构
[1] Cent S Univ, Dept Rehabil, Cardiac Rehabil Ctr, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
关键词
astragaloside IV; platelet-derived growth factor; vascular smooth muscle cell; proliferation; migration; OXIDATIVE STRESS; UP-REGULATION; NEOINTIMAL HYPERPLASIA; PDGF-BB; PATHWAY; PHENOTYPE; PROTEIN; ANGIOGENESIS; ACCUMULATION; SUPPRESSES;
D O I
10.3892/etm.2014.1905
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Astragaloside IV (AS-IV), the major active component extracted from Astragalus membranaceus, has been demonstrated to exhibit protective effects on the cardiovascular, immune, digestive and nervous systems; thus, has been widely used in traditional Chinese medicine. Abnormal proliferation and migration of vascular smooth muscle cells (VSMCs) is closely associated with the initiation and progression of cardiovascular diseases, including atherosclerosis and restenosis. However, the effects of AS-IV on VSMCs remain unknown. For the first time, the present study demonstrated that AS-IV markedly suppressed platelet-derived growth factor (PDGF)-BB-stimulated cellular proliferation and migration of HDMEC-a human dermal VSMCs (HDVSMCs). Further investigation into the underlying molecular mechanisms demonstrated that the administration of AS-IV attenuated the PDGF-BB-stimulated switch of HDVSMCs into a proliferative phenotype. Furthermore, AS-IV inhibited the PDGF-BB-induced expression of cell cycle-associated proteins, as well as the upregulation of matrix metalloproteinase (MMP)2, but not MMP9. In addition, AS-IV was shown to downregulate the activation of p38 mitogen-activated protein kinase (MAPK) signaling induced by PDGF-BB in HDVSMCs. Therefore, the observations of the present study indicate that AS-IV inhibits PDGF-BB-stimulated VSMC proliferation and migration, possibly by inhibiting the activation of the p38 MAPK signaling pathway. Thus, AS-IV may be useful for the treatment of vascular diseases.
引用
收藏
页码:1253 / 1258
页数:6
相关论文
共 30 条
[1]
Oxidative stress modulates vascular smooth muscle cell phenotype via CTGF in thoracic aortic aneurysm [J].
Branchetti, Emanuela ;
Poggio, Paolo ;
Sainger, Rachana ;
Shang, Eric ;
Grau, Juan B. ;
Jackson, Benjamin M. ;
Lai, Eric K. ;
Parmacek, Michael S. ;
Gorman, Robert C. ;
Gorman, Joseph H. ;
Bavaria, Joseph E. ;
Ferrari, Giovanni .
CARDIOVASCULAR RESEARCH, 2013, 100 (02) :316-324
[2]
DHEA inhibits vascular remodeling following arterial injury: a possible role in suppression of inflammation and oxidative stress derived from vascular smooth muscle cells [J].
Chen, Jiangbin ;
Xu, Lin ;
Huang, Congxin .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2014, 388 (1-2) :75-84
[3]
PDGF-Induced Migration of Vascular Smooth Muscle Cells Is Inhibited by Heme Oxygenase-1 Via VEGFR2 Upregulation and Subsequent Assembly of Inactive VEGFR2/PDGFRβ Heterodimers [J].
Cheng, Caroline ;
Haasdijk, Remco A. ;
Tempel, Dennie ;
den Dekker, Wijnand K. ;
Chrifi, Ihsan ;
Blonden, Lau A. J. ;
van de Kamp, Esther H. M. ;
de Boer, M. ;
Burgisser, Petra E. ;
Noorderloos, Annemarie ;
Rens, Joost A. P. ;
ten Hagen, Timo L. M. ;
Duckers, Henricus J. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (05) :1289-+
[4]
The microRNA miR-132 targets Lrrfip1 to block vascular smooth muscle cell proliferation and neointimal hyperplasia [J].
Choe, Nakwon ;
Kwon, Jin-Sook ;
Kim, Ju-Ryoung ;
Eom, Gwang Hyeon ;
Kim, Yongsook ;
Nam, Kwang-Il ;
Ahn, Youngkeun ;
Kee, Hae Jin ;
Kook, Hyun .
ATHEROSCLEROSIS, 2013, 229 (02) :348-355
[5]
MiRNA-146a regulates the maturation and differentiation of vascular smooth muscle cells by targeting NF-κB expression [J].
Dong, Shaohong ;
Xiong, Wei ;
Yuan, Jianhui ;
Li, Jianghua ;
Liu, Jianjun ;
Xu, Xinyun .
MOLECULAR MEDICINE REPORTS, 2013, 8 (02) :407-412
[6]
Platelet-derived growth factor signaling in mesenchymal cells [J].
Donovan, Johanna ;
Abraham, David ;
Norman, Jill .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2013, 18 :106-119
[7]
RETRACTED: Rosuvastatin suppresses platelet-derived growth factor-BB-induced vascular smooth muscle cell proliferation and migration via the MAPK signaling pathway (Retracted Article) [J].
Gan, Jianting ;
Li, Ping ;
Wang, Zhengdong ;
Chen, Jian ;
Liang, Xiangwen ;
Liu, Ming ;
Xie, Wenchao ;
Yin, Ruixing ;
Huang, Feng .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2013, 6 (04) :899-903
[8]
Inhibitory Effects of Brazilin on the Vascular Smooth Muscle Cell Proliferation and Migration Induced by PDGF-BB [J].
Guo, Jing ;
Li, Li ;
Wu, Yu-Jie ;
Yan, Yu ;
Xu, Xiao-Na ;
Wang, Shou-Bao ;
Yuan, Tian-Yi ;
Fang, Lian-Hua ;
Du, Guan-Hua .
AMERICAN JOURNAL OF CHINESE MEDICINE, 2013, 41 (06) :1283-1296
[9]
Titanium dioxide nanoparticles increase inflammatory responses in vascular endothelial cells [J].
Han, Sung Gu ;
Newsome, Bradley ;
Hennig, Bernhard .
TOXICOLOGY, 2013, 306 :1-8
[10]
Platelet-derived growth factor BB mediates the glioma-induced migration of bone marrow-derived mesenchymal stem cells by promoting the expression of vascular cell adhesion molecule-1 through the PI3K, P38 MAPK and NF-κB pathways [J].
Hu, Yi ;
Cheng, Peng ;
Ma, Jiang-Chun ;
Xue, Yi-Xue ;
Liu, Yun-Hui .
ONCOLOGY REPORTS, 2013, 30 (06) :2755-2764