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首页> 外文期刊>FEBS Letters >Mildly oxidised LDL induces more macrophage death than moderately oxidised LDL: roles of peroxidation, lipoprotein‐associated phospholipase A2 and PPARγ
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Mildly oxidised LDL induces more macrophage death than moderately oxidised LDL: roles of peroxidation, lipoprotein‐associated phospholipase A2 and PPARγ

机译:轻度氧化的LDL比中度氧化的LDL诱导更多的巨噬细胞死亡:过氧化,脂蛋白相关磷脂酶A2和PPARγ的作用

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>Death of macrophages and smooth muscle cells (SMC) can lead to progression of atherosclerosis. Mildly oxidised low-density lipoprotein (mildly-oxLDL) induced more overall death and apoptosis than moderately oxidised LDL, in human monocyte-macrophages (HMM). Mildly-oxLDL also induced more overall death in human SMC than did moderately-oxLDL. Mildly-oxLDL contained more hydroperoxides, but less oxysterol, malondialdehyde and negative charge than moderately-oxLDL. Specific inhibition of lipoprotein-associated phospholipase A2 (by SB222657) diminished death induction in HMM by both oxLDL types. Peroxisome proliferator-activated receptor γ (PPARγ) antagonist (GW9662) and agonist (ciglitazone) experiments suggested that non-hydrolysed, oxidised phospholipids in oxLDL activate PPARγ as a cellular defence mechanism. These results may be relevant to LDL oxidation within atherosclerotic plaques and may suggest strategies for combating atherosclerosis progression.
机译:>巨噬细胞和平滑肌细胞(SMC)的死亡可导致动脉粥样硬化的发展。在人单核巨噬细胞(HMM)中,轻度氧化的低密度脂蛋白(mildly-oxLDL)比中度氧化的LDL引起更多的整体死亡和细胞凋亡。与中度-oxLDL相比,轻度-oxLDL还诱导了更多的人SMC整体死亡。与中度-oxLDL相比,轻度-oxLDL包含更多的氢过氧化物,但氧固醇,丙二醛和负电荷较少。脂蛋白相关的磷脂酶A 2 (由SB222657)的特异性抑制作用可减少两种oxLDL类型的HMM的死亡诱导。过氧化物酶体增殖物激活受体γ(PPARγ)拮抗剂(GW9662)和激动剂(西格列酮)实验表明,oxLDL中未水解的氧化磷脂激活PPARγ作为细胞防御机制。这些结果可能与动脉粥样硬化斑块内的低密度脂蛋白氧化有关,并可能提示对抗动脉粥样硬化进展的策略。

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