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Comparison of the cytotoxic, pro-oxidant and pro-inflammatory characteristics of different oxysterols

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Abstract

Oxidized low-density lipoproteins play important roles in the development of atherosclerosis and contain several lipid-derived, bioactive molecules which are believed to contribute to atherogenesis. Of these, some cholesterol oxidation products, refered to as oxysterols, are suspected to favor the formation of atherosclerotic plaques involving cytotoxic, pro-oxidant and pro-inflammatory processes. Ten commonly occurring oxysterols (7α-, 7β-hydroxycholesterol, 7-ketocholesterol, 19-hydroxycholesterol, cholesterol-5α,6α-epoxide, cholesterol-5β,6β-epoxide, 22R-, 22S-, 25-, and 27-hydroxycholesterol) were studied for both their cytotoxicity and their ability to induce superoxide anion production (O2⋅ −) and IL-8 secretion in U937 human promonocytic leukemia cells. Cytotoxic effects (phosphatidylserine externalization, loss of mitochondrial potential, increased permeability to propidium iodide, and occurrence of cells with swollen, fragmented and/or condensed nuclei) were only identified with 7β-hydroxycholesterol, 7-ketocholesterol and cholesterol-5β,6β-epoxide, which also induce lysosomal destabilization associated or not associated with the formation of monodansylcadaverine-positive cytoplasmic structures. No relationship between oxysterol-induced cytotoxicity and HMG-CoA reductase activity was found. In addition, the highest O2⋅ − overproduction quantified with hydroethidine was identified with 7β-hydroxycholesterol, 7-ketocholesterol and cholesterol-5β,6β-epoxide, with cholesterol-5α, 6α-epoxide and 25-hydroxycholesterol. The highest capacity to simultaneously stimulate IL-8 secretion (quantified by ELISA and by using a multiplexed, particle-based flow cytometric assay) and enhance IL-8 mRNA levels (determined by RT-PCR) was observed with 7β-hydroxycholesterol and 25-hydroxycholesterol. None of the effects observed for the oxysterols were detected for cholesterol. Therefore, oxysterols may have cytotoxic, oxidative, and/or inflammatory effects, or none whatsoever.

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Abbreviations

AO:

acridine orange

MDC:

monodansylcadaverine

HE:

hydroethidine

HMG-CoA:

3-hydroxy-3-methylglutaryl-CoA reductase

PE:

phycoerythrin

References

  • Aupeix K, Weltin D, Mejia JE, et al. Oxysterol-induced apoptosis in human monocytic cell lines. Immunobiol. 1995;194:415–28.

    Google Scholar 

  • Bansal N, Houle AG, Melnykovych G. Comparison of dexamethasone and lovastatin (mevinolin) as growth inhibitors in cultures of T cell derived human acute leukaemia lines (CEM). Leuk Res. 1989;13:875–82.

    Article  PubMed  Google Scholar 

  • Berliner JA, Heinecke JW. The role of oxidized lipoproteins in atherogenesis. Free Radic Biol Med. 1996;20:707–27.

    Article  PubMed  Google Scholar 

  • Berthier A, Lemaire-Ewing S, Prunet C, et al. Involvement of a calcium-dependent dephosphorylation of BAD associated with the localization of Trpc-1 within lipid rafts in 7-ketocholesterol-induced THP-1 cell apoptosis. Cell Death Differ. 2004;11:897–905.

    Article  PubMed  Google Scholar 

  • Beseme F, Astruc ME, Defay R, Crastes de Paulet A. Rat liver cytosol oxysterol-binding protein. FEBS Lett. 1987;210:97–103.

    Article  PubMed  Google Scholar 

  • Boisvert WA. Modulation of atherogenesis by chemokines. Trends Cardiovasc Med. 2004;14:161–5.

    Article  PubMed  Google Scholar 

  • Brown AJ, Jessup W. Oxysterols and atherosclerosis. Atherosclerosis. 1999;142:1–28.

    Article  PubMed  Google Scholar 

  • Brown MS, Goldstein JL. Suppression of 3-hydroxy-3-methyl- glutaryl coenzyme A reductase activity and inhibition of growth of human fibroblasts by 7-ketocholesterol. J Biol Chem. 1974;249:7306–14.

    PubMed  Google Scholar 

  • Chen LB. Mitochondrial membrane potential in living cells. Annu Rev Cell Biol. 1988;4:155–81.

    Article  PubMed  Google Scholar 

  • Colles SM, Maxson JM, Carlson SG, Chisolm GM. Oxidized LDL-induced injury and apoptosis in atherosclerosis: potential roles for oxysterols. Trends Cardiovasc Med. 2001;11:131–8.

    Article  PubMed  Google Scholar 

  • De Nigris F, Lerman A, Ignarro LJ, et al. Oxidation-sensitive mechanisms, vascular apoptosis and atherosclerosis. Trends Mol Med. 2003;9:351–9.

    Article  PubMed  Google Scholar 

  • Dzeletovic S, Babiker A, Lund E, Diczfalusy U. Time course of oxy-sterol formation during in vitro oxidation of low density lipoprotein. Chem Phys Lipids. 1995;78:119–28.

    Article  PubMed  Google Scholar 

  • Feng B, Yao PM, Li Y, et al. The endoplasmic reticulum is the site of cholesterol-induced cytotoxicity in macrophages. Nature Cell Biol. 2003;5:781–92.

    Article  PubMed  Google Scholar 

  • Garcia-Cruset S, Carpenter KL, Guardiola F, Mitchinson MJ. Oxy-sterols in cap and core of human advanced atherosclerotic lesions. Free Radic Res. 1999;30:341–50.

    PubMed  Google Scholar 

  • Guicciardi ME, Deussing J, Miyoshi H, et al. Cathepsin B contributes to TNF-α mediated hepatocyte apoptosis by promoting mitochondrial release of cytochrome c. J Clin Invest. 2000;106:1127–37.

    PubMed  Google Scholar 

  • Guijarro C, Blanco-Colio LM, Ortego M, et al. 3-Hydoxy-3-methylglutaryl coenzyme A reductase and isoprenylation inhibitors induce apoptosis of vascular smooth cells in culture. Circ Res. 1998;83:490–500.

    PubMed  Google Scholar 

  • Hansson GK. Immune mechanisms in atherosclerosis. Arterioscler Thromb Vasc Biol. 2001;21:1876–90.

    PubMed  Google Scholar 

  • Hwang PLH. High-affinity binding sites for oxygenated sterols in rat liver microsomes: possible identity with anti-estrogen binding sites. Biochim Biophys Acta 1990;1033:154–61.

    Google Scholar 

  • Ishisaka R, Utsumi T, Kamo T, et al. Participation of a cathepsin L-type protease in the activation of caspase-3. Cell Struct Funct. 1999;24:465–70.

    Article  PubMed  Google Scholar 

  • Iuliano L, Micheletta F, Natoli S, et al. Measurement of oxysterols and α-tocopherol in plasma and tissue samples as indices of oxidant stress status. Anal Biochem. 2003;312:217–23.

    Article  PubMed  Google Scholar 

  • Janowski BA, Grogan MJ, Jones SA, et al. Structural requirements of ligands for the oxysterol liver X receptors LXRα and LXRβ. Proc Natl Acad Sci USA. 1999;96:266–71.

    Article  PubMed  Google Scholar 

  • Kahn E, Vejux A, Lizard G, et al. Analysis of the fluorescence of monodansyl cadacerine positive cytoplasmic structures during 7-ketocholesterol-induced cell death. Anal Quant Cytol Histol. 2004;27:47–56.

    Google Scholar 

  • Kandutsch AA, Taylor FR, Shown EP. Different forms of the oxysterol-binding protein. Binding kinetics and stability. J Biol Chem. 1984;259:12388–97.

    Google Scholar 

  • Kellar KL, Iannone MA. Multiplexed microsphere-based flow cytometric assays. Exp Hematol. 2002;30:1227–37.

    Article  PubMed  Google Scholar 

  • Kockx MM, Knaapen MWM. The role of apoptosis in vascular disease. J Pathol. 2001;190:267–80.

    Article  Google Scholar 

  • Lazier CB, Bapat BV. Antioestrogen binding sites: general and comparative properties. J Steroid Biochem. 1988;31:665–9.

    Article  PubMed  Google Scholar 

  • Lemaire S, Lizard G, Monier S, et al. Different patterns of IL-1β secretion, adhesion molecule expression and apoptosis induction in human endothelial cells treated with 7α-,7β-hydroxycholesterol, or 7-ketocholesterol. FEBS Lett. 1998;440:434–9.

    Article  PubMed  Google Scholar 

  • Li W, Dalen H, Eaton JW, Yuan XM. Apoptotic death of inflammatory cells in human atheroma. Arterioscler Thromb Vasc Biol. 2001;21:1124–30.

    PubMed  Google Scholar 

  • Liu Y, Hulten LM, Wiklund O. Macrophages isolated from human atherosclerotic plaques produce IL-8, and oxysterols may have a regulatory function for IL-8 production. Arterioscler Thromb Vasc Biol. 1997;17:317–23.

    PubMed  Google Scholar 

  • Lizard G, Deckert V, Dubrez L, Moisant M, Gambert P, Lagrost L. Induction of apoptosis in endothelial cells treated with cholesterol oxides. Am J Pathol. 1996;148:1625–38.

    PubMed  Google Scholar 

  • Lizard G, Fournel S, Genestier L, et al. Kinetics of plasma membrane and mitochondrial alterations in cells undergoing apoptosis. Cytometry. 1995;21:275–83.

    Article  PubMed  Google Scholar 

  • Lizard G, Gueldry S, Sordet O, et al. Glutathione is implied in the control of 7-ketocholesterol-induced apoptosis, which is associated with radical oxygen species production. FASEB J. 1998;12:1651–63.

    PubMed  Google Scholar 

  • Lizard G, Monier S, Cordelet C, et al. Characterization and comparison of the mode of cell death, apoptosis versus necrosis, induced by 7β-hydroxycholesterol and 7-ketocholesterol in the cells of the vascular wall. Arterioscler Thromb Vasc Biol. 1999;19:1190–200.

    PubMed  Google Scholar 

  • Miguet C, Monier S, Bettaieb A, et al. Ceramide generation occurring during 7β-hydroxycholesterol- and 7-ketocholesterol-induced apoptosis is caspase independent and is not required to trigger cell death. Cell Death Differ. 2001;8:83–99.

    Article  PubMed  Google Scholar 

  • Miguet-Alfonsi C, Prunet C, Monier S, et al. Analysis of oxidative processes and of myelin figures formation before and after the loss of mitochondrial transmembrane potential during 7β-hydroxycholesterol and 7-ketocholesterol-induced apoptosis: comparison with various pro-apoptotic chemicals. Biochem Pharm. 2002;64:527–41.

    Article  PubMed  Google Scholar 

  • Monier S, Samadi M, Prunet C, et al. Impairment of the cytotoxic and oxidative activities of 7β-hydroxycholesterol and 7-ketocholesterol by esterification with oleate. Biochem Biophys Res Commun. 2003;303:814–24.

    Article  PubMed  Google Scholar 

  • Moreau M, Brocheriou I, Petit L, Ninio E, Chapman MJ, Rouis M. Interleukin-8 mediates downregulation of tissue inhibitor of metalloproteinase-1 expression in cholesterol-loaded human macrophages: relevance to stability of atherosclerotic plaque. Circulation. 1999;99:420–6.

    PubMed  Google Scholar 

  • Morgan E, Varro R, Sepulveda H, et al. Cytometric bead array: multiplexed assay platform with applications in various areas of biology. Clin Immunol. 2004;110:252–66.

    Article  PubMed  Google Scholar 

  • Mügge A. The role of reactive oxygen species in atherosclerosis. Z Kardiol. 1998;87:851–64.

    Article  PubMed  Google Scholar 

  • O’Callaghan JC, Woods JA, O’Brien NM. Comparative study of the cytotoxicity and apoptosis-inducing potential of commonly occurring oxysterols. Cell Biol Toxicol. 2001;17:127–37.

    Article  PubMed  Google Scholar 

  • Olkkonen VM. Oxysterol binding protein and its homologues: new regulatory factors involved in lipid metabolism. Curr Opin Lipidol. 2004;15:321–7.

    Article  PubMed  Google Scholar 

  • Olsson GM, Rungby J, Rundquist I, Brunk UT. Evaluation of lysosomal stability in living cultured macrophages by cytofluorometry. Effect of silver lactate and hypotonic solutions. Virchows Archiv B Cell Pathol. 1989;56:263–9.

    Google Scholar 

  • Olsson M, Rundquist I, Brunk U. Flow cytofluorometry of lysosomal acridine orange uptake by living cultured cells. Acta Pathol Microbiol Immunol Scand (Sect A). 1987;95:159–65.

    Google Scholar 

  • Rosenblat M, Aviram M. Oxysterol-induced activation of macrophage NADPH-oxidase enhances cell-mediated oxidation of LDL in the atherosclerotic apolipoprotein E deficient mouse: inhibitory role for vitamin E. Atherosclerosis. 2002;160:69–80.

    Article  PubMed  Google Scholar 

  • Rothe G, Valet G. Flow cytometric analysis of respiratory burst activity in phagocytes with hydroethidine and 2′,7′-dichlorofluorescin. J Leukoc Biol. 1990;47:440–8.

    PubMed  Google Scholar 

  • Salonen JT, Nyyssonen K, Salonen R, et al. Lipoprotein oxidation and progression of atherosclerosis. Circulation. 1997;95:840–5.

    PubMed  Google Scholar 

  • Sleer LS, Brown AJ, Stanley KK. Interaction of caveolin with 7-ketocholesterol. Atherosclerosis. 2001;159:49–55.

    Article  PubMed  Google Scholar 

  • Smith LL. Cholesterol autoxidation. Chem Phys Lipids. 1987;44:87–125.

    Article  PubMed  Google Scholar 

  • Tabas I. Consequences of cellular cholesterol accumulation: basic concepts and physiological implications. J Clin Invest. 2002;110:905–11.

    Article  PubMed  Google Scholar 

  • Terkeltaub R, Banka CL, Solan J, Santoro D, Brand K, Curtiss LK. Oxidized LDL induces monocytic cell expression of interleukin-8, a chemokine with T-lymphocyte chemotactic activity. Arterioscler Thromb. 1994;14:47–53.

    PubMed  Google Scholar 

  • Vaya J, Aviram M, Mahmood S, et al. Selective distribution of oxy-sterols in atherosclerotic lesions and human plasma lipoproteins. Free Radic Res. 2001;34:485–97.

    PubMed  Google Scholar 

  • Vermes I, Haanen C, Steffens-Nakken H, Reutelingsperger C. A novel assay for apoptosis: flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled annexin V. J Immunol Methods. 1995;184:39– 51.

    Article  PubMed  Google Scholar 

  • Vignali DAA. Multiplexed particle-based flow cytometric assays. J Immunol Methods. 2000;243:243–55.

    Article  PubMed  Google Scholar 

  • Wang N, Tabas I, Winchester R, Ravalli S, Rabbani LE, Tall A. Interleukin 8 is induced by cholesterol loading of macrophages and expressed by macrophage foam cells in human atheroma. J Biol Chem. 1996;15:8837–42.

    Google Scholar 

  • Witztum JL, Steinberg D. The oxidative modification hypothesis of atherosclerosis: does it hold for humans? Trends Cardiovasc Med. 2001;11:93–102.

    Article  PubMed  Google Scholar 

  • Yasunobu Y, Hayashi K, Shingu T, Yamagata T, Kajiyama G, Kambe M. Coronary atherosclerosis and oxidative stress as reflected by autoantibodies against low-density lipoprotein and oxysterols. Atherosclerosis. 2001;155:445–53.

    Article  PubMed  Google Scholar 

  • Yeh CG, His B, Faulk WP. Propidium iodide as a nuclear marker in immunofluorescence. II. Use with cellular identification and viability studies. J Immunol Methods. 1981;43:269–75.

    Google Scholar 

  • Yin J, Chaufour X, McLachlan C, et al. Apoptosis of vascular smooth muscle cells induced by cholesterol and its oxides in vitro and in vivo. Atherosclerosis. 2000;148:365–74.

    Article  PubMed  Google Scholar 

  • Yuan XM, Li W, Brunk UT, Dalen H, Chang YH, Sevanian A. Lysosomal dstabilization during macrophage damage induced by cholesterol oxidation products. Free Radic Biol Med. 2000;28:208–18.

    Article  PubMed  Google Scholar 

  • Ziedén B, Kaminskas A, Kristenson M, et al. Increased plasma 7β-hydroxycholesterol concentrations in a population with a high risk for cardiovascular disease. Arterioscler Thromb Vasc Biol. 1999;19:967–71.

    PubMed  Google Scholar 

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Lemaire-Ewing, S., Prunet, C., Montange, T. et al. Comparison of the cytotoxic, pro-oxidant and pro-inflammatory characteristics of different oxysterols. Cell Biol Toxicol 21, 97–114 (2005). https://doi.org/10.1007/s10565-005-0141-2

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