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抑制胞质磷脂酶A2可通过游离胆固醇的再酯化作用抑制胆固醇酯的产生,但不会抑制氧化型低密度脂蛋白刺激的巨噬细胞中泡沫细胞的形成。

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.

作者信息

Ii Hiromi, Oka Mayuko, Yamashita Atsushi, Waku Keizo, Uozumi Naonori, Shimizu Takao, Sato Takashi, Akiba Satoshi

机构信息

Department of Pathological Biochemistry, Kyoto Pharmaceutical University, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan.

出版信息

Biol Pharm Bull. 2008 Jan;31(1):6-12. doi: 10.1248/bpb.31.6.

Abstract

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(2)s (cPLA(2)s) in the production of CE through the reesterification and in the formation of foam cells. In [(3)H]oleic acid-labeled human acute monocytic leukemia (THP-1) cell-derived macrophages (THP-M) and mouse peritoneal macrophages (MPM), which possessed at least cPLA(2)alpha and cPLA(2)gamma, stimulation with OxLDL induced the production of [(3)H]cholesteryl oleate ([(3)H]CE).The production was suppressed by an inhibitor of cPLA(2)s. 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(2)alpha-knockout MPM, OxLDL-induced increases in [(3)H]CE and total CE did not differ from those in wild-type MPM. Our results suggest that cPLA(2)s other than cPLA(2)alpha 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.

摘要

巨噬细胞源性泡沫细胞的形成是胆固醇酯(CE)蓄积的结果,CE不仅蓄积于细胞质中(在细胞质中,通过对经历水解的氧化低密度脂蛋白(OxLDL)衍生的游离胆固醇进行再酯化来产生CE),还蓄积于溶酶体中(在溶酶体中沉积着OxLDL剩余的CE)。我们研究了胞质磷脂酶A2(cPLA2)通过再酯化参与CE生成以及参与泡沫细胞形成的可能性。在用[³H]油酸标记的人急性单核细胞白血病(THP-1)细胞源性巨噬细胞(THP-M)和小鼠腹腔巨噬细胞(MPM)中,这两种细胞至少拥有cPLA2α和cPLA2γ,用OxLDL刺激可诱导产生[³H]胆固醇油酸酯([³H]CE)。cPLA2的抑制剂可抑制这种生成。然而,该抑制剂往往会使细胞内CE的总水平略有降低,并且如用油红O染色所估计的那样,并不影响泡沫细胞的形成。在cPLA2α基因敲除的MPM中,OxLDL诱导的[³H]CE和总CE的增加与野生型MPM中的增加没有差异。我们的结果表明,除cPLA2α外,cPLA2在OxLDL刺激的巨噬细胞中有助于脂肪酸的供应,这些脂肪酸通过再酯化用于CE的生成。然而,仅通过抑制cPLA2介导的CE生成并不能抑制泡沫细胞的形成。

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