Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway

1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh Schoo...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2007-07, Vol.293 (1), p.H770-H776
Hauptverfasser: Villacorta, Luis, Zhang, Jifeng, Garcia-Barrio, Minerva T, Chen, Xi-lin, Freeman, Bruce A, Chen, Yuqing E, Cui, Taixing
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container_end_page H776
container_issue 1
container_start_page H770
container_title American journal of physiology. Heart and circulatory physiology
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creator Villacorta, Luis
Zhang, Jifeng
Garcia-Barrio, Minerva T
Chen, Xi-lin
Freeman, Bruce A
Chen, Yuqing E
Cui, Taixing
description 1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Submitted 2 March 2007 ; accepted in final form 27 April 2007 Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology. nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1 Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu )
doi_str_mv 10.1152/ajpheart.00261.2007
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The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology. nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1 Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. 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Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Submitted 2 March 2007 ; accepted in final form 27 April 2007 Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. 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Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>293</volume><issue>1</issue><spage>H770</spage><epage>H776</epage><pages>H770-H776</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Submitted 2 March 2007 ; accepted in final form 27 April 2007 Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology. nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1 Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17468336</pmid><doi>10.1152/ajpheart.00261.2007</doi><oa>free_for_read</oa></addata></record>
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source MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Animals
Cell Proliferation - drug effects
Cells, Cultured
Cellular biology
Cyclin-Dependent Kinase Inhibitor p27 - metabolism
Dose-Response Relationship, Drug
Fatty acids
Inhibitor drugs
Intracellular Signaling Peptides and Proteins
Kelch-Like ECH-Associated Protein 1
Kinases
Linoleic Acids - administration & dosage
Male
Muscle, Smooth, Vascular - cytology
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - physiology
Myocytes, Smooth Muscle - cytology
Myocytes, Smooth Muscle - drug effects
Myocytes, Smooth Muscle - physiology
NF-E2-Related Factor 2 - metabolism
Nitric oxide
Nitro Compounds - administration & dosage
Proteins - metabolism
Rats
Rats, Sprague-Dawley
Signal Transduction - drug effects
Signal Transduction - physiology
Studies
title Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway
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