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Oxidative stress-responsive apoptosis-inducing protein in patients with heterozygous familial hypercholesterolemia
Heart and Vessels ( IF 1.4 ) Pub Date : 2021-07-26 , DOI: 10.1007/s00380-021-01898-9
Kayoko Sato 1 , Takako Yao 2 , Tsutomu Fujimura 3 , Kimie Murayama 4 , Ko Okumura 5 , Nobuhisa Hagiwara 1 , Yoshinori Seko 5
Affiliation  

Oxidative stress, an inducer of apoptosis, plays a critical role in ischemia/reperfusion injury and atherosclerosis. We previously identified an apoptosis-inducing ligand, the post-translationally modified secreted form of eukaryotic translation initiation factor 5A (eIF5A), ‘oxidative stress-responsive apoptosis-inducing protein’ (ORAIP). In this study, we investigated the role of ORAIP in patients with heterozygous familial hypercholesterolemia (HeFH), a leading cause of premature cardiovascular disease. We analyzed plasma ORAIP and oxidized low-density lipoprotein (oxLDL) levels in 60 patients with HeFH (60% male, 57.0 ± 13.6 years of age) and 20 patients with LDL-C hypercholesterolemia (DL, 85% male, 64.1 ± 13.3 years of age). The coronary artery atherosclerosis from the patients with HeFH who had a coronary artery bypass graft was investigated by double immunostaining. The plasma ORAIP levels in the patients with HeFH were significantly elevated compared to those in the patients with DL (73.5 ± 46.0 vs. 48.3 ± 21.4 ng/mL, p = 0.0277). The plasma oxLDL levels in HeFH patients were also elevated (156.8 ± 65.2 vs. 123.7 ± 46.6 mg/dL, p = 0.0461) compared to those in DL patients and correlated with maxLDL-C levels (R = 0.4454, p = 0.00648). Double-immunostaining of ORAIP and oxLDL in the coronary artery from patients with HeFH who had a coronary artery bypass graft showed that ORAIP and oxLDL were colocalized with apoptotic vascular smooth muscle cells in the atherosclerotic plaque. ORAIP plays a role in the development of oxidative stress-induced atherosclerosis and may be an important therapeutic target for plaque rupture in patients with HeFH.



中文翻译:

杂合子家族性高胆固醇血症患者的氧化应激反应性凋亡诱导蛋白

氧化应激是细胞凋亡的诱导剂,在缺血/再灌注损伤和动脉粥样硬化中起关键作用。我们之前鉴定了一种凋亡诱导配体,即翻译后修饰的真核翻译起始因子 5A (eIF5A) 的分泌形式,“氧化应激反应性凋亡诱导蛋白”(ORAIP)。在这项研究中,我们调查了 ORAIP 在杂合子家族性高胆固醇血症 (HeFH) 患者中的作用,HeFH 是过早心血管疾病的主要原因。我们分析了 60 名 HeFH 患者(60% 男性,57.0 ± 13.6 岁)和 20 名 LDL-C 高胆固醇血症患者(DL,85% 男性,64.1 ± 13.3 岁)的血浆 ORAIP 和氧化低密度脂蛋白 (oxLDL) 水平年龄)。通过双重免疫染色研究了接受冠状动脉旁路移植术的 HeFH 患者的冠状动脉粥样硬化。与 DL 患者相比,HeFH 患者的血浆 ORAIP 水平显着升高(73.5 ± 46.0 vs. 48.3 ± 21.4 ng/mL,p  = 0.0277)。与 DL 患者相比,HeFH 患者的血浆 oxLDL 水平也升高(156.8 ± 65.2 vs. 123.7 ± 46.6 mg/dL,p  = 0.0461),并且与 maxLDL-C 水平相关(R  = 0.4454,p  = 0.00648)。对接受冠状动脉旁路移植术的 HeFH 患者冠状动脉中 ORAIP 和 oxLDL 的双重免疫染色显示,ORAIP 和 oxLDL 与动脉粥样硬化斑块中的凋亡血管平滑肌细胞共定位。ORAIP 在氧化应激诱导的动脉粥样硬化的发展中发挥作用,可能是 HeFH 患者斑块破裂的重要治疗靶点。

更新日期:2021-07-26
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