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Differentially-expressed genes related to atherosclerosis in acrolein-stimulated human umbilical vein endothelial cells

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Abstract

Acrolein is a highly reactive α, β-unsaturated aldehyde that is an environmental pollutant, a product of endogenous lipid peroxidation and a major component of cigarette smoke, which has been linked to the development of atherosclerotic vascular disease. Activation of endothelial cells by stimuli such as cigarette smoke is an important risk factor in atherosclerosis. Several studies have reported that acrolein levels are increased in atherosclerosis. Presently, a whole human DNA chip containing 24,000 genes was utilized to examine atherogenesis-related gene expression profiles of acrolein-stimulated human umbilical vein endothelial cells (HUVECs). Genes whose expression changed more than 2-fold included 3,174 up-regulated genes and 551 down-regulated genes. The affected genes included human atherogenesis-related genes such as cytokines, chemokines and adhesion molecules. These results support the view that acrolein-stimulated changes in HUVEC gene expression contribute to the development of atherosclerosis.

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References

  1. Berliner, J.A. & Heinecke, J.W. The role of oxidized lipoproteins in atherogenesis. Free Radic. Biol. Med. 20, 707–727 (1996).

    Article  CAS  Google Scholar 

  2. Stocker, R. & Keaney, J.F., Jr. Role of oxidative modifications in atherosclerosis. Physiol. Rev. 84, 1381–1478 (2004).

    Article  CAS  Google Scholar 

  3. Victor, V.M. et al. Oxidative stress, endothelial dysfunction and atherosclerosis. Curr. Pharm. Des. 15, 2988–3002 (2009).

    Article  CAS  Google Scholar 

  4. He, J. et al. Risk factors for congestive heart failure in US men and women: NHANES I epidemiologic follow-up study. Arch. Intern. Med. 161, 996–1002 (2001).

    Article  CAS  Google Scholar 

  5. Ockene, I.S. & Miller, N.H. Cigarette smoking, cardiovascular disease, and stroke: a statement for healthcare professionals from the American Heart Association. American Heart Association Task Force on Risk Reduction. Circulation 96, 3243–3247 (1997).

    CAS  Google Scholar 

  6. Black, H. Smoking and cardiovascular disease. Hypertension: Pathophysiology, Diagnosis and Management 2v, 2621–2647 (1995).

    Google Scholar 

  7. Lee, S.H. et al. Identification of atherosclerosis related gene expression profiles by treatment of Benzo(a)-pyrene in human umbilical vein endothelial cells. Mol. Cell. Toxicol. 5, 113–119 (2009).

    Google Scholar 

  8. Barnoya, J. & Glantz, S.A. Cardiovascular effects of secondhand smoke: nearly as large as smoking. Circulation 111, 2684–2698 (2005).

    Article  Google Scholar 

  9. Carmella, S.G. et al. Quantitation of acrolein-derived (3-hydroxypropyl) mercapturic acid in human urine by liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry: effects of cigarette smoking. Chem. Res. Toxicol. 20, 986–990 (2007).

    Article  CAS  Google Scholar 

  10. Talhout, R., Opperhuizen, A. & van Amsterdam, J.G. Sugars as tobacco ingredient: Effects on mainstream smoke composition. Food. Chem. Toxicol. 44, 1789–1798 (2006).

    Article  CAS  Google Scholar 

  11. Marnett, L.J., Riggins, J.N. & West, J.D. Endogenous generation of reactive oxidants and electrophiles and their reactions with DNA and protein. J. Clin. Invest. 111, 583–593 (2003).

    CAS  Google Scholar 

  12. LoPachin, R.M. & Barber, D.S. Synaptic cysteine sulfhydryl groups as targets of electrophilic neurotoxicants. Toxicol. Sci. 94, 240–255 (2006).

    Article  CAS  Google Scholar 

  13. Calingasan, N.Y., Uchida, K. & Gibson, G.E. Proteinbound acrolein: a novel marker of oxidative stress in Alzheimer’s disease. J. Neurochem. 72, 751–756 (1999).

    Article  CAS  Google Scholar 

  14. Shao, B. et al. Acrolein impairs ATP binding cassette transporter A1-dependent cholesterol export from cells through site-specific modification of apolipoprotein A-I. J. Biol. Chem. 280, 36386–36396 (2005).

    Article  CAS  Google Scholar 

  15. Hamann, K. et al. Critical role of acrolein in secondary injury following ex vivo spinal cord trauma. J. Neurochem. 107, 712–721 (2008).

    Article  CAS  Google Scholar 

  16. Hamann, K., Nehrt, G., Ouyang, H., Duerstock, B. & Shi, R. Hydralazine inhibits compression and acroleinmediated injuries in ex vivo spinal cord. J. Neurochem. 104, 708–718 (2008).

    CAS  Google Scholar 

  17. Luo, J. & Shi, R. Acrolein induces axolemmal disruption, oxidative stress, and mitochondrial impairment in spinal cord tissue. Neurochem. Int. 44, 475–486 (2004).

    Article  CAS  Google Scholar 

  18. Conklin, D.J. et al. Acrolein generation stimulates hypercontraction in isolated human blood vessels. Toxicol. Appl. Pharmacol. 217, 277–288 (2006).

    Article  CAS  Google Scholar 

  19. McCall, M.R., Tang, J.Y., Bielicki, J.K. & Forte, T.M. Inhibition of lecithin-cholesterol acyltransferase and modification of HDL apolipoproteins by aldehydes. Arterioscler. Thromb. Vasc. Biol. 15, 1599–1606 (1995).

    CAS  Google Scholar 

  20. Alfredsson, L., Hammar, N. & Hogstedt, C. Incidence of myocardial infarction and mortality from specific causes among bus drivers in Sweden. Int. J. Epidemiol. 22, 57–61 (1993).

    Article  CAS  Google Scholar 

  21. Hoffmann, D., Melikian, A.A. & Brunnemann, K.D. Studies in tobacco carcinogenesis. IARC Sci. Publ. 482–484 (1991).

  22. Ranganna, K. et al. Acrolein activates mitogen-activated protein kinase signal transduction pathways in rat vascular smooth muscle cells. Mol. Cell. Biochem. 240, 83–98 (2002).

    Article  CAS  Google Scholar 

  23. Lee, N.J., Lee, S.E., Lee, S.H., Ryu, D.S. & Park, Y.S. Acrolein induces adaptive response through upregulate of HO-1 via activation of Nrf2 in RAW 264.7 macrophage. Mol. Cell. Toxicol. 5, 230–236 (2009).

    Google Scholar 

  24. Kachel, D.L. & Martin, W.J., 2nd. Cyclophosphamideinduced lung toxicity: mechanism of endothelial cell injury. J. Pharmacol. Exp. Ther. 268, 42–46 (1994).

    CAS  Google Scholar 

  25. Lovell, M.A., Xie, C. & Markesbery, W.R. Acrolein is increased in Alzheimer’s disease brain and is toxic to primary hippocampal cultures. Neurobiol. Aging. 22, 187–194 (2001).

    Article  CAS  Google Scholar 

  26. Puranik, R. & Celermajer, D.S. Smoking and endothelial function. Prog. Cardiovasc. Dis. 45, 443–458 (2003).

    Article  CAS  Google Scholar 

  27. Gross, C.M. et al. Angiotensin II type 1 receptor expression in human coronary arteries with variable degrees of atherosclerosis. Basic Res. Cardiol. 97, 327–333 (2002).

    Article  CAS  Google Scholar 

  28. Zernecke, A., Shagdarsuren, E. & Weber, C. Chemokines in atherosclerosis: an update. Arterioscler. Thromb. Vasc. Biol. 28, 1897–1908 (2008).

    Article  CAS  Google Scholar 

  29. Amoruso, A. et al. Enhanced peroxisome proliferators-activated receptor-gamma expression in monocyte/macrophages from coronary artery disease patients and possible gender differences. J. Pharmacol. Exp. Ther. 331, 531–538 (2009).

    Article  CAS  Google Scholar 

  30. Rozenberg, O., Rosenblat, M., Coleman, R., Shih, D.M. & Aviram, M. Paraoxonase (PON1) deficiency is associated with increased macrophage oxidative stress: studies in PON1-knockout mice. Free Radic. Biol. Med. 34, 774–784 (2003).

    Article  CAS  Google Scholar 

  31. Kawakami, A. et al. Toll-like receptor 2 mediates apolipoprotein CIII-induced monocyte activation. Circ. Res. 103, 1402–1409 (2008).

    Article  CAS  Google Scholar 

  32. Kurisaki, A. et al. The mechanism of nuclear export of Smad3 involves exportin 4 and Ran. Mol. Cell. Biol. 26, 1318–1332 (2006).

    Article  CAS  Google Scholar 

  33. Park, Y.S. et al. Acrolein induces cyclooxygenase-2 and prostaglandin production in human umbilical vein endothelial cells: roles of p38 MAP kinase. Arterioscler. Thromb. Vasc. Biol. 27, 1319–1325 (2007).

    Article  CAS  Google Scholar 

  34. Lee, S.E. et al. Uncaria rhynchophylla induces heme oxygenase-1 as a cytoprotective effect in RAW 264.7 macrophages. Mol. Cell. Toxicol. 6, 33–40 (2010).

    Article  CAS  Google Scholar 

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Correspondence to Yong Seek Park.

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Lee, S.E., Lee, S.H., Ryu, D.S. et al. Differentially-expressed genes related to atherosclerosis in acrolein-stimulated human umbilical vein endothelial cells. BioChip J 4, 264–271 (2010). https://doi.org/10.1007/s13206-010-4402-7

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  • DOI: https://doi.org/10.1007/s13206-010-4402-7

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