Influence of oxidized low density lipoprotein on the proliferation of human artery smooth muscle cells in vitro

Chenhui Qiao , Kailun Zhang , Jiahong Xia

Current Medical Science ›› 2007, Vol. 27 ›› Issue (6) : 20 -23.

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Current Medical Science ›› 2007, Vol. 27 ›› Issue (6) : 20 -23. DOI: 10.1007/s11596-007-0106-1
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Influence of oxidized low density lipoprotein on the proliferation of human artery smooth muscle cells in vitro

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Abstract

The effects of oxidized low density lipoprotein (ox-LDL) on the proliferation of cultured human vascular smooth muscle cells (vSMC) were investigated in vitro. By using NaBr density gradient centrifugation, LDL was isolated and purified from human plasma. Ox-LDL was produced from LDL by being incubated with CuSO4. ox-LDL was then added to the culture medium at different concentrations (35, 60, 85, 110, 135 and 160 μg/mL) for 7 days. The influence of ox-LDL on vSMC proliferation was observed in growth curve, mitosis index, and in situ determination of apoptosis. The data were analyzed with SPSS 10.0 software. The results showed that the ox-LDL produced in vitro had a good purity and optimal oxidative degree, which was similar to the intrinsic ox-LDL in atherosclerotic plaque. ox-LDL at a concentration of 35 μg/mL demonstrated the strongest proliferation inducement, and at a concentration of 135 μg/mL, ox-LDL could inhibit the growth of vSMC. ox-LDL at concentrations of 35 and 50 μg/mL presented powerful mitotic trigger, and with the increase of ox-LDL concentration, the mitotic index of vSMC was decreased gradually. ox-LDL at higher concentrations promoted more apoptotic vSMCs. ox-LDL at lower concentrations triggered proliferation of vSMCs, and at higher concentrations induced apoptosis in vSMCs. ox-LDL played a promotional role in the pathogenesis and development of atherosclerosis by affecting vSMC proliferation and apoptosis.

Keywords

oxidized low density lipoprotein / smooth muscle cell / proliferation / atherosclerosis

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Chenhui Qiao, Kailun Zhang, Jiahong Xia. Influence of oxidized low density lipoprotein on the proliferation of human artery smooth muscle cells in vitro. Current Medical Science, 2007, 27(6): 20-23 DOI:10.1007/s11596-007-0106-1

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References

[1]

SteinbergD., ParthasarathyS., CarewT. E., et al.. Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity. N Enge J Med, 1989, 320(14): 915-924

[2]

SteinbrecherU. P., ZhangH. F., LougheedM.. Role of oxidatively modified LDL in atherosclerosis. Free Radic Biol Med, 1990, 9: 155-168

[3]

ArgmannC. A., SawyezC. G., LiS., et al.. Human smooth muscle cell subpopulations differentially accumulate cholesteryl ester when exposed to native and oxidized lipoproteins. Arterioscler Thromb Vasc Biol, 2004, 24: 1290-1296

[4]

MayrM., XuQ.. Smooth muscle cell apoptosis in arteriosclerosis. Exp Gerontol, 2001, 36: 969-87

[5]

KohnoM., YokokawaK., YasunariK., et al.. Effect of natriuretic peptide family on the oxidized LDL-induced migration of human coronary artery smooth muscle cells. Circ Res, 1997, 81: 585-590

[6]

WellsK. E., MiguelR., AlexanderJ. J., et al.. Transmembrane calcium flux regulates LDL oxidation by arterial smooth muscle cells. J Surg Res, 1997, 67: 126-131

[7]

ZhaoG. F., GaoP., ZhangH., et al.. Cloning the full length cDNA of a gene responsible for vascular smooth muscle cell proliferation in atherogenesis and study of function. Chin Med J, 2003, 116: 166-170

[8]

LiH. H., GuS. M., CaoX. Y., et al.. Suppression of induced atherosclerosis in H-apo AI transgenic mice by overexpression of human apo AI in the aortic wall. Chin Med J, 2000, 113: 657-661

[9]

TepeG., DudaS. H., MedingJ., et al.. Tc-99m-labeled endothelin derivative for imaging of experimentally induced atherosclerosis. Atherosclerosis, 2001, 157: 383-392

[10]

AlexanderJ. J., LewisI.. The influence of platelet-smooth muscle cell interaction on the oxidative modification of low-density lipoprotein. J Surg Res, 2002, 103: 41-46

[11]

ShenC. M., MaoS. J., HuangG. S.. Stimulation of smooth muscle cell proliferation by ox-LDL-and acetyl LDL-induced macrophage-derived foam cells. Life Sci, 2001, 70: 443-452

[12]

NorataG. D., TontiL., RomaP., et al.. Apoptosis and proliferation of endothelial cells in early atherosclerotic lesions: possible role of oxidised LDL. Nutr Metab, Cardiovasc Dis, 2002, 12: 297-305

[13]

TaguchiS., OinumaT., YamadaT.. A comparative study of cultured smooth muscle cell proliferation and injury, utilizing glycated low density lipoproteins with slight oxidation, auto-oxidation, or extensive oxidation. J Atheroscler Thromb, 2000, 7: 132-137

[14]

NatarajanV., ScribnerW. M., HartC. M., et al.. Oxidized low density lipoprotein-mediated activation of phospholipase D in smooth muscle cells: a possible role in cell proliferation and atherogenesis. J Lipid Res, 1995, 36: 2005-2016

[15]

NorataG. D., TontiL., RomaP., et al.. Apoptosis and proliferation of endothelial cells in early atherosclerotic lesions: possible role of oxidised LDL. Nutr Metab, Cardiovasc Dis, 2002, 12: 297-305

[16]

CarpenterK. L., ChallisI. R., ArendsM. J.. Mildly oxidised LDL induces more macrophage death than moderately oxidised LDL: roles of peroxidation, lipoprotein-associated phospholipase A2 and PPARgamma. FEBS Lett, 2003, 553: 145-150

[17]

NapoliC., QuehenbergerO., De NigrisF., et al.. Mildly oxidized low density lipoprotein activates multiple apoptotic signaling pathways in human coronary cells. FASEB J, 2000, 14: 1996-2007

[18]

KohnoM., YokokawaK., YasunariK., et al.. Effect of natriuretic peptide family on the oxidized LDL-induced migration of human coronary artery smooth muscle cells. Circ Res, 1997, 81: 585-590

[19]

BachemM. G., WendelinD., SchneiderhanW., et al.. Depending on their concentration oxidized low density lipoproteins stimulate extracellular matrix synthesis or induce apoptosis in human coronary artery smooth muscle cells. Clin Chem Lab Med, 1999, 37: 319-326

[20]

ZhouY. F., GuettaE., YuZ. X., et al.. Human cytomegalovirus increases modified low density lipoprotein uptake and scavenger receptor mRNA expression in vascular smooth muscle cells. J Clin Invest, 1996, 98: 2129-2138

[21]

MayrM., XuQ.. Smooth muscle cell apoptosis in arteriosclerosis. Exp Gerontol, 2001, 36: 969-987

[22]

ThorneS. A., AbbotS. E., WinyardP. G., et al.. Extent of oxidative modification of low density lipoprotein determines the degree of cytotoxicity to human coronary artery cells. Heart, 1996, 75: 11-16

[23]

MataP., VarelaO., AlonsoR., et al.. Monounsaturated and polyunsaturated n-6 fatty acid-enriched diets modify LDL oxidation and decrease human coronary smooth muscle cell DNA synthesis. Arterioscler Thromb Vasc Biol, 1997, 17: 2088-2095

[24]

VerhammeP., QuarckR., HaoH., et al.. Dietary cholesterol withdrawal reduces vascular inflammation and induces coronary plaque stabilization in miniature pigs. Cardiovasc Res, 2002, 56: 135-144

[25]

NigrisF., YoussefT., CiafreS., et al.. Evidence for oxidative activation of c-Myc-dependent nuclear signaling in human coronary smooth muscle cells and in early lesions of Watanabe heritable hyperlipidemic rabbits: protective effects of vitamin E. Circulation, 2000, 102: 2111-2117

[26]

VriesC. J., AchiterbergT. A., HorrevoetsA. J., et al.. Differential display identification of 40 genes with altered expression in activated human smooth muscle cells. Local expression in atherosclerotic lesions of smags, smooth muscle activation-specific genes. J Biol Chem, 2000, 275: 23 939-23 947

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