Effects of lycopene on the induction of foam cell formation by modified LDL.

Napolitano, M., De Pascale, C., Wheeler-Jones, C., Botham, K.M. and Bravo, E. 2007. Effects of lycopene on the induction of foam cell formation by modified LDL. American Journal of Physiology: Endocrinology and Metabolism. 293 (6), pp. E1820-7. https://doi.org/10.1152/ajpendo.00315.2007

TitleEffects of lycopene on the induction of foam cell formation by modified LDL.
AuthorsNapolitano, M., De Pascale, C., Wheeler-Jones, C., Botham, K.M. and Bravo, E.
Abstract

The effect of lycopene on macrophage foam cell formation induced by modified low-density lipoprotein (LDL) was studied. Human monocyte-derived macrophages (HMDM) were incubated with lycopene in the presence or absence of native LDL (nLDL) or LDL modified by oxidation (oxLDL), aggregation (aggLDL), or acetylation (acLDL). The cholesterol content, lipid synthesis, scavenger receptor activity, and the secretion of inflammatory [interleukin (IL)-1β and tumor necrosis factor (TNF)-α] and anti-inflammatory (IL-10) cytokines was determined. Lycopene was found to decrease the synthesis of cholesterol ester in incubations without LDL or with oxLDL while triacylglycerol synthesis was reduced in the presence of oxLDL and aggLDL. Scavenger receptor activity as assessed by the uptake of acLDL was decreased by ∼30% by lycopene. In addition, lycopene inhibited IL-10 secretion by up to 74% regardless of the presence of nLDL or aggLDL but did not affect IL-1β or TNF-α release. Lycopene also reduced the relative abundance of mRNA transcripts for scavenger receptor A (SR-A) in THP-1 macrophages treated with aggLDL. These findings suggest that lycopene may reduce macrophage foam cell formation induced by modified LDL by decreasing lipid synthesis and downregulating the activity and expression of SR-A. However, these effects are accompanied by impaired secretion of the anti-inflammatory cytokine IL-10, suggesting that lycopene may also exert a concomitant proinflammatory effect.

JournalAmerican Journal of Physiology: Endocrinology and Metabolism
Journal citation293 (6), pp. E1820-7
ISSN0193-1849
Year2007
PublisherAmerican Physiological Society
Digital Object Identifier (DOI)https://doi.org/10.1152/ajpendo.00315.2007
Publication dates
Published01 Dec 2016

Related outputs

Populated Collagen Hydrogel and Polyhydroxyalkanoate Composites: Novel Matrices for Cartilage Repair and Regeneration?
De Pascale, C., Marcello, E., Getting, S.J., Roy, I. and Locke, I.C. Forthcoming. Populated Collagen Hydrogel and Polyhydroxyalkanoate Composites: Novel Matrices for Cartilage Repair and Regeneration? OARSI World Congress on Osteoarthritis . Toronto, Canada 02 Mar - 05 May 2019

Effect of Urocortin on human osteoclasts differentiation
De Pascale, C. 2018. Effect of Urocortin on human osteoclasts differentiation. Getting, S.J. and Locke, I.C. (ed.) British Pharmacological Society Meeting. the Queen Elizabeth II Conference Centre 18 - 20 Dec 2018 British Pharmacological Society.

Influence of chylomicron remnants on human monocyte activation in vitro
Bentley, C., Hathaway, N., Widdows, J., Bejta, F., De Pascale, C., Avella, M., Wheeler-Jones, C.P.D., Botham, K.M. and Lawson, C. 2011. Influence of chylomicron remnants on human monocyte activation in vitro. Nutr Metab Cardiovasc Dis.. 21 (11), pp. 871-878. https://doi.org/10.1016/j.numecd.2010.02.019

Suppression of nuclear factor-kappaB activity in macrophages by chylomicron
De Pascale, C., Graham, V., Fowkes, R.C., Wheeler-Jones, C.P. and Botham, K.M. 2010. Suppression of nuclear factor-kappaB activity in macrophages by chylomicron. European Atherosclerosis Society Meeting . Hamburg, germany 20 - 23 Jun 2010 Elsevier. https://doi.org/10.1016/S1567-5688(10)70301-9

P221 lipid droplets in human macrophages recruit cytosolic phospholipase A2 and promote secretion of inflammatory mediators
De Pascale, C., Bostrom, P., Wickström, Y., Mogensen, C., MattssonHultén, L., Perkins, R., Ståhlman, M., Wiklund, O., Olofsson, S.-O. and Borén, J. 2010. P221 lipid droplets in human macrophages recruit cytosolic phospholipase A2 and promote secretion of inflammatory mediators. European Atherosclerosis Society (EAS) Conference. Hamburg 20 - 23 Jun 2010 Elsevier. https://doi.org/10.1016/S1567-5688(10)70288-9

Modulation of CYP1A1 by PKC Inhibitors and TPA Pre-Treatments in MH1C1 Rat Hepatoma Cells Exposed to 3 -Methylcholanthrene
De Pascale, C., Domenicotti, C., Nitti, M., Marengo, B., Catalano, M., Scanarotti, C., Sanguineti, R., Siri, M., Ledda, S., Penco, S. and Bassi, A. 2009. Modulation of CYP1A1 by PKC Inhibitors and TPA Pre-Treatments in MH1C1 Rat Hepatoma Cells Exposed to 3 -Methylcholanthrene. The Open Toxicology Journal . (3), pp. 47-57. https://doi.org/10.2174/1874340400903010047

Suppression of nuclear factor-κB activity in macrophages by chylomicron remnants: modulation by the fatty acid composition of the particles
De Pascale, C., Graham, V., Fowkes, R.C., Wheeler-Jones, C.P.D. and Botham, K.M. 2009. Suppression of nuclear factor-κB activity in macrophages by chylomicron remnants: modulation by the fatty acid composition of the particles. FEBS Journal. 276 (19), pp. 5689-5702. https://doi.org/10.1111/j.1742-4658.2009.07260.x

Characterization of three human sec14p-like proteins: a-Tocopherol
Zingg, J.M., Kempna, P., Paris, M., Reiter, E., Villacorta, L., Cipollone, R., Munteanu, A., De Pascale, C., Menini, S., Cueff, A., Arock, M., Azzi, A. and Ricciarelli, R. 2008. Characterization of three human sec14p-like proteins: a-Tocopherol. Biochimie . 90 (11-12), p. 1703–1715. https://doi.org/10.1016/j.biochi.2008.07.008

The induction of macrophages foam cell formation by chylomicron remnants
Botham, K.M., Moore, E.H., De Pascale, C. and Bejta, F. 2007. The induction of macrophages foam cell formation by chylomicron remnants. Biochemical Society Transactions. 35 (3), pp. 454-458. https://doi.org/10.1042/BST0350454

Dietary fats induce human monocyte activation in vitro
Bentley, C., Bejta, F., De Pascale, C., Avella, M., Wheeler-Jones, C.P.D., Botham, K.M. and Lawson, C. 2007. Dietary fats induce human monocyte activation in vitro. Biochemical Society Transactions. 35 (3), pp. 464-465. https://doi.org/10.1042/BST0350464

Increased expression of transglutaminase-1 and PPARgamma after vitamin E treatment in human keratinocytes
De Pascale, M.C., Bassi, A.M., Patrone, V., Villacorta, L., Azzi, A. and Zing, J.M. 2006. Increased expression of transglutaminase-1 and PPARgamma after vitamin E treatment in human keratinocytes. Archives of Biochemistry and Biophysics. 447 (2), pp. 97-106. https://doi.org/10.1016/j.abb.2006.02.002

Fatty acids composition of Chylomicron remnants like particles influences their uptake and induction of lipid accumulation in macrophages.
De Pascale, C., Avella, M., Perona, J.S., Ruiz-Gutierrez, V., Wheeler-Jones, C.P.D. and Botham, K.M. 2006. Fatty acids composition of Chylomicron remnants like particles influences their uptake and induction of lipid accumulation in macrophages. FEBS Journal . 273 (24), p. 5632–5640. https://doi.org/10.1111/j.1742-4658.2006.05552.x

Antioxidant status in J774A.1 macrophage cell line during chronic exposure to glycated serum
Bassi, A.M., Ledda, S., De Pascale, M.C., Penco, S., Rossi, S., Odetti, P. and Cottalasso, D. 2005. Antioxidant status in J774A.1 macrophage cell line during chronic exposure to glycated serum. Biochemistry and Cell Biology. 83 (2), pp. 176-87. https://doi.org/10.1139/o05-024

Damaging effects of advanced glycation end product in the murine macrophages cell line J774A.1.
Bassi, A.M., Ledda, S., Valentini, S., De Pascale, M.C., Rossi, S., Odetti, P. and Cottalasso, D. 2002. Damaging effects of advanced glycation end product in the murine macrophages cell line J774A.1. Toxicology In Vitro. 16 (4), pp. 339-347. https://doi.org/10.1016/S0887-2333(02)00016-4

Permalink - https://westminsterresearch.westminster.ac.uk/item/9y208/effects-of-lycopene-on-the-induction-of-foam-cell-formation-by-modified-ldl


Share this

Usage statistics

88 total views
0 total downloads
These values cover views and downloads from WestminsterResearch and are for the period from September 2nd 2018, when this repository was created.