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早期动脉粥样硬化病变中15-脂氧合酶mRNA和蛋白的诱导

Induction of 15-lipoxygenase mRNA and protein in early atherosclerotic lesions.

作者信息

Hiltunen T, Luoma J, Nikkari T, Ylä-Herttuala S

机构信息

Department of Medical Biochemistry, Medical School, University of Tampere, Finland.

出版信息

Circulation. 1995 Dec 1;92(11):3297-303. doi: 10.1161/01.cir.92.11.3297.

Abstract

BACKGROUND

15-Lipoxygenase (15-LO) may be involved in atherogenesis and in oxidative modification of LDL. In this study, we investigated 15-LO expression in developing atherosclerotic lesions and verified the exact type of the atherosclerosis-associated LO at the nucleotide level.

METHODS AND RESULTS

Quantitative reverse transcription-polymerase chain reaction, in situ hybridization, and immunocytochemistry were used in two models of experimental atherosclerosis. New Zealand White rabbits were given a 1% cholesterol diet for 0 (control group), 3, 6, or 14 weeks. 15-LO mRNA was undetectable in the aortic intima-medias of the control group, whereas it was clearly induced as early as after 3 weeks. 15-LO expression increased further in the 6- and 14-week groups. According to in situ hybridization and immunocytochemical studies, 15-LO was localized to macrophagerich areas. In Watanabe heritable hyperlipidemic rabbits, 15-LO mRNA was undetectable in normal aortic intima-medias. 15-LO mRNA was markedly induced in fatty streaks but less so in more advanced lesions. Identification of the induced LO as reticulocyte-type 15-LO was done by cloning and sequencing. We also observed a distinct basal expression of copper-zinc and extracellular superoxide dismutases in normal aortic intima-medias, but no clear induction of these mRNAs was detected in atherosclerotic aortas.

CONCLUSIONS

The results show that, in contrast to copper-zinc and extracellular superoxide dismutases, the expression of reticulocyte-type 15-LO is markedly induced in rabbit fatty streaks. This may lead to an increase in the oxidative potential during the early phase of atherogenesis and contribute to the development of atherosclerotic lesions.

摘要

背景

15-脂氧合酶(15-LO)可能参与动脉粥样硬化的发生以及低密度脂蛋白的氧化修饰。在本研究中,我们调查了15-LO在动脉粥样硬化病变发展过程中的表达情况,并在核苷酸水平上验证了与动脉粥样硬化相关的脂氧合酶的确切类型。

方法与结果

在两种实验性动脉粥样硬化模型中采用定量逆转录-聚合酶链反应、原位杂交和免疫细胞化学方法。给新西兰白兔喂食1%胆固醇饮食0周(对照组)、3周、6周或14周。对照组主动脉内膜-中膜中未检测到15-LO mRNA,而早在3周后就明显诱导表达。在6周和14周组中15-LO表达进一步增加。根据原位杂交和免疫细胞化学研究,15-LO定位于富含巨噬细胞的区域。在渡边遗传性高脂血症兔中,正常主动脉内膜-中膜中未检测到15-LO mRNA。15-LO mRNA在脂肪条纹中明显诱导表达,但在更晚期病变中诱导程度较低。通过克隆和测序鉴定诱导的脂氧合酶为网织红细胞型15-LO。我们还观察到正常主动脉内膜-中膜中铜锌超氧化物歧化酶和细胞外超氧化物歧化酶有明显的基础表达,但在动脉粥样硬化主动脉中未检测到这些mRNA的明显诱导。

结论

结果表明,与铜锌超氧化物歧化酶和细胞外超氧化物歧化酶不同,网织红细胞型15-LO的表达在兔脂肪条纹中明显诱导。这可能导致动脉粥样硬化发生早期氧化潜能增加,并有助于动脉粥样硬化病变的发展。

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