Cigarette smoke extract promotes human vascular smooth muscle cell proliferation and survival through ERK1/2- and NF-κB-dependent pathways

20Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Tobacco use is one of the major risk factors of cardiovascular disease. The underlying molecular mechanisms that link cigarette smoke to cardiovascular disease remain unclear. The present study was designed to examine the effects of dimethyl sulfoxide (DMSO)-soluble smoke particles (DSPs) on human aortic smooth muscle cell (HASMC) cultures, and to explore the mitogen-activated protein kinase (MAPK)/extracellular signal-regulated protein kinase 1 and 2 (ERK1/2) and nuclear factor-kappaB (NF-κB) signal mechanisms involved. Serum-starved HASMCs were treated with DSPs for up to 48 h. DSPs promoted cell proliferation in a concentration-dependent manner from 0.05 to 0.2 μl/ml. Activation of ERK1/2 and NF-κB was seen after exposure to DSPs. This occurred in parallel with the increase in cell population, bromodeoxyuridine incorporation, and cyclinD1/cyclin-dependent kinase 4 expression. Blocking phosphorylation of ERK1/2 by MAPK inhibitors U0126 and PD98059, and inhibiting activation of NF-κB by IkappaB (IκB) kinase inhibitors wedelolactone or IMD-0354, abolished the DSP effects. However, either a p38 inhibitor (SB203580) or an inhibitor of lipopolysaccharide (polymyxin B), or nicotinic receptor blockers (mecamylamine and á-bungarotoxin), did not inhibit a DSPinduced increase in the cell population. DSPs increased the expression of intercellular adhesion molecule 1 and the release of interleukin-6 in HASMCs, both of which were inhibited by ERK1/2 or NF-κB pathway inhibitors. Furthermore, cell apoptosis and necrosis were found in serum-starved HASMCs. DSPs decreased cell death and increased B-cell leukemia/lymphoma 2 expression. Blocking phosphorylation of ERK1/2 or NF-κB attenuated DSP-induced cell death inhibition. Cigarette smoke particles stimulate HASMC proliferation and inhibit cell death. The intracellular signal mechanisms behind this involve activation of ERK1/2 and NF-κB pathways. ©2010 with author. Published by TheScientificWorld.

References Powered by Scopus

MAPK signal pathways in the regulation of cell proliferation in mammalian cells

2128Citations
N/AReaders
Get full text

The pathophysiology of cigarette smoking and cardiovascular disease: An update

1856Citations
N/AReaders
Get full text

Embryonic lethality and liver degeneration in mice lacking the rela component of NF-κB

1669Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Understanding the pathogenesis of abdominal aortic aneurysms

277Citations
N/AReaders
Get full text

Cigarette smoke and inflammation: Role in cerebral aneurysm formation and rupture

117Citations
N/AReaders
Get full text

Understanding the effects of tobacco smoke on the pathogenesis of aortic aneurysm

105Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Chen, Q. W., Edvinsson, L., & Xu, C. B. (2010). Cigarette smoke extract promotes human vascular smooth muscle cell proliferation and survival through ERK1/2- and NF-κB-dependent pathways. TheScientificWorldJournal, 10, 2139–2156. https://doi.org/10.1100/tsw.2010.201

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 8

47%

Researcher 5

29%

Professor / Associate Prof. 3

18%

Lecturer / Post doc 1

6%

Readers' Discipline

Tooltip

Medicine and Dentistry 4

33%

Agricultural and Biological Sciences 3

25%

Biochemistry, Genetics and Molecular Bi... 3

25%

Chemistry 2

17%

Save time finding and organizing research with Mendeley

Sign up for free