Inhibition of Cytosolic Phospholipase A_2 Suppresses Production of Cholesteryl Ester through the Reesterification of Free Cholesterol but not Formation of Foam Cells in Oxidized LDL-Stimulated Macrophages(Highlighted paper selected by Editor-in-chief,Bioc
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概要
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Macrophage-derived foam cells are formed as a result of the accumulation of cholesteryl ester (CE) not only in cytoplasm where CE is produced by the reesterification of free cholesterol derived from oxidized low density lipoprotein (OxLDL) undergoing hydrolysis, but also in lysosomes where the remaining CE of OxLDL is deposited. We examined the possible involvement of cytosolic phospholipase A_2s (cPLA_2s) in the production of CE through the reesterification and in the formation of foam cells. In [^3H]oleic acid-labeled human acute monocytic leukemia (THP-1) cell-derived macrophages (THP-M) and mouse peritoneal macrophages (MPM), which possessed at least cPLA_2α and cPLA_2γ, stimulation with OxLDL induced the production of [^3H]cholesteryl oleate ([^3H]CE).The production was suppressed by an inhibitor of cPAL_2s. However, the inhibitor tended to slightly decrease total intracellular levels of CE, and did not affect the formation of foam cells, as estimated by staining with Oil Red O. In cPLA_2α-knockout MPM, OxLDL-induced increases in [^3H]CE and total CE did not differ from those in wild-type MPM. Our results suggest that cPLA_2s other than cPLA_2α contribute to the supply of fatty acids, which are utilized for the production of CE through the reesterification, in OxLDL-stimulated macrophages. However, the formation of foam cells could not be inhibited only by the suppression of cPLA_2-mediated CE production.
- 2008-01-01
著者
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SATO Takashi
Department of Neurosurgery, University of Yamanashi, Faculty of Medicine
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WAKU Keizo
Faculty of Pharmaceutical Sciences, Teikyo University
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II Hiromi
Department of Pathological Biochemistry, Kyoto Pharmaceutical University
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OKA Mayuko
Department of Pathological Biochemistry, Kyoto Pharmaceutical University
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YAMASHITA Atsushi
Faculty of Pharmaceutical Sciences, Teikyo University
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UOZUMI Naonori
Department of Biochemistry and Molecular Biology, Faculty of Medicine, The University of Tokyo
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SHIMIZU Takao
Department of Biochemistry and Molecular Biology, Faculty of Medicine, The University of Tokyo
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AKIBA Satoshi
Department of Pathological Biochemistry, Kyoto Pharmaceutical University
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Waku Keizo
Faculty Of Pharmaceutical Science Teikyo University
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Oka Mayuko
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Uozumi Naonori
Department Of Biochemistry And Molecular Biology Faculty Of Medicine The University Of Tokyo
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Ii Hiromi
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Akiba S
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Akiba Satoshi
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Yamashita Atsushi
Faculty Of Pharmaceutical Sciences Teikyo University
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Sato Takashi
Department Of Internal Medicine And Clinical Immunology Yokohama City University School Of Medicine
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Shimizu Takao
Department Of Biochemistry And Molecular Biology Faculty Of Medicine The University Of Tokyo
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Sato Takashi
Department Of Pathological Biochemistry Kyoto Pharmaceutical University
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Sato Takashi
Department Of Communications And Computer Engineering Kyoto University
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Sato Takashi
Department Of Applied Biochemistry And Food Science Saga University
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