Chisolm G M, Ma G, Irwin K C, Martin L L, Gunderson K G, Linberg L F, Morel D W, DiCorleto P E
Department of Cell Biology, Cleveland Clinic Foundation, OH 44195.
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11452-6. doi: 10.1073/pnas.91.24.11452.
Modification of low density lipoprotein (LDL) by free radical oxidation renders this molecular complex cytotoxic. Oxidized lipoproteins exist in vivo in atherosclerotic lesions and in the plasma of diabetic animals, suggesting that lipoprotein-induced tissue damage may occur in certain diseases. We undertook purification and identification of the major cytotoxin in oxidized LDL. The lipid extract from oxidized LDL was subjected to multiple HPLC separations, and the fractions were assayed for cytotoxicity. Mass spectrometry and nuclear magnetic resonance identified the purified toxin as 7 beta-hydroperoxycholest-5-en-3 beta-ol (7 beta-OOH-Chol). This molecule accounted for approximately 90% of the cytotoxicity of the lipids of oxidized LDL. We also found 7 beta-OOH-Chol in human atherosclerotic lesions from endarterectomy specimens obtained immediately after excision. These results are consistent with the hypothesis that the oxidized LDL present in lesions has the capacity to induce cell and tissue injury, leading to progression of the disease and the generation of the necrotic core of the lesion.
低密度脂蛋白(LDL)经自由基氧化修饰后会使这种分子复合物具有细胞毒性。氧化型脂蛋白存在于动脉粥样硬化病变的体内以及糖尿病动物的血浆中,这表明脂蛋白诱导的组织损伤可能在某些疾病中发生。我们对氧化型LDL中的主要细胞毒素进行了纯化和鉴定。将氧化型LDL的脂质提取物进行多次高效液相色谱分离,并对各馏分进行细胞毒性测定。质谱分析和核磁共振鉴定纯化后的毒素为7β-氢过氧胆甾-5-烯-3β-醇(7β-OOH-Chol)。该分子约占氧化型LDL脂质细胞毒性的90%。我们还在动脉内膜切除标本切除后立即获得的人类动脉粥样硬化病变中发现了7β-OOH-Chol。这些结果与以下假设一致:病变中存在的氧化型LDL具有诱导细胞和组织损伤的能力,导致疾病进展和病变坏死核心的形成。