Title Chemerin Stimulates Vascular Smooth Muscle Cell Proliferation and Carotid Neointimal Hyperplasia by Activating Mitogen-Activated Protein Kinase Signaling
Authors Xiong, Wei
Luo, Yu
Wu, Lin
Liu, Feng
Liu, Huadong
Li, Jianghua
Liao, Bihong
Dong, Shaohong
Affiliation Jinan Univ, Shenzhen Peoples Hosp, Dept Cardiol, Clin Med Coll 2, NO 1017,Dongmen North Rd, Shenzhen 518020, Peoples R China.
Peking Univ, Hosp 1, Dept Cardiol, 8 Xishiku St, Beijing 100034, Peoples R China.
Keywords EPICARDIAL ADIPOSE-TISSUE
METABOLIC SYNDROME
ENDOTHELIAL-CELLS
CORONARY-ARTERY
RECEPTOR CCRL2
ELUTING STENTS
EXPRESSION
ATHEROSCLEROSIS
INFLAMMATION
ADIPOKINE
Issue Date 2016
Publisher PLOS ONE
Citation PLOS ONE.2016,11(10).
Abstract Vascular neointimal hyperplasia and remodeling arising from local inflammation are characteristic pathogeneses of proliferative cardiovascular diseases, such as atherosclerosis and post angioplasty restenosis. The molecular mechanisms behind these pathological processes have not been fully determined. The adipokine chemerin is associated with obesity, metabolism, and control of inflammation. Recently, chemerin has gained increased attention as it was found to play a critical role in the development of cardiovascular diseases. In this study, we investigated the effects of chemerin on the regulation of vascular smooth muscle cells and carotid neointimal formation after angioplasty. We found that circulating chemerin levels increased after carotid balloon injury, and that knockdown of chemerin significantly inhibited the proliferative aspects of vascular smooth muscle cells induced by platelet-derived growth factor-BB and pro-inflammatory chemokines in vitro as well as prohibited carotid neointimal hyperplasia and pro-inflammatory chemokines in vivo after angioplasty. Additionally, inhibition of chemerin down-regulated the expression of several proteins, including phosphorylated p38 mitogen-activated protein kinase, phosphorylated extracellular signal regulated kinase 1/2, nuclear factor-kappa B p65, and proliferation cell nuclear antigen. The novel finding of this study is that chemerin stimulated vascular smooth muscle cells proliferation and carotid intimal hyperplasia through activation of the mitogen-activated protein kinase signaling pathway, which may lead to vascular inflammation and remodeling, and is relevant to proliferative cardiovascular diseases.
URI http://hdl.handle.net/20.500.11897/457203
ISSN 1932-6203
DOI 10.1371/journal.pone.0165305
Indexed SCI(E)
PubMed
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