A new beating heart model of cardiopulmonary bypass-induced acute kidney injury demonstrates heme protein toxicity and ferroptosis.

IF 3.8 3区 医学 Q1 UROLOGY & NEPHROLOGY
Kathryn Smedlund, Dulat Bekbolsynov, Mustafa Azizi, Apurva Lad, Sareeta Manandhar, William T Gunning, Sebastian V Jansen, Lasse J Strudthoff, David E Leaf, Stanislaw Stepkowski, Rajesh Gupta
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引用次数: 0

Abstract

Background: Cardiac surgery-associated acute kidney injury (CSA-AKI) occurs in 20-30% of patients after heart surgery with cardiopulmonary bypass (CPB). AKI rates are even higher in VA ECMO treated patients. The pathogenesis of CSA-AKI is incompletely understood, and preventative therapies are lacking. We hypothesize that CSA-AKI occurs due to pump related RBC hemolysis and accumulation of cell-free hemoglobin (CFH) and hemopexin in the kidneys.

Methods: A new beating heart model of CPB was developed. Rats were used for CPB experiments; blood pressure (BP) was measured by Millar invasive BP catheters, and Glomerular Filtration Rate (GFR) was measured at 24 hours after CPB using the FITC-Sinistrin (FITC-S) method. Western immunoblots were performed to measure hemopexin (Hpx), glutathione peroxidase 4 (GPX4), and β-actin. Urine KIM-1 was measured by ELISA method. KIM-1 and TATA-box Binding Protein 1 (TBP1) mRNA expression were quantified by qRT-PCR. Plasma levels of cell-free hemoglobin (CFH), Hpx, haptoglobin, and IL-6 were measured by ELISA. Immunofluorescence labeling was used to detect hemoglobin (Hb), Hpx, megalin, and KIM-1 in kidneys. Lipid peroxidation was assessed with 4-hydroxynonenal (4-HNE) staining.

Results: Compared with sham controls, GFR was reduced 24 hours after CPB and histological kidney sections had higher scores, indicating CPB-induced AKI. Urine KIM-1 protein level and kidney KIM-1 mRNA were increased after CPB. Immunofluorescence staining also showed tubular KIM-1 staining after CPB. Plasma IL-6 levels were increased after CPB, and plasma Hpx increased 24 hours after CPB. Immunofluorescence staining demonstrated colocalized Hpx and megalin in proximal tubules in kidneys, with hemoglobin staining in kidneys after CPB. Finally, ferroptosis was induced by CPB, as evidenced by decreased GPX4 protein and increased 4-HNE staining at 24 hrs. after CPB.

Conclusion: CPB induces AKI with evidence of hemoglobin and Hpx deposition in the proximal tubules and ferroptosis.

一种新的体外循环急性肾损伤心脏跳动模型显示血红素蛋白毒性和铁上吊。
背景:心脏手术相关急性肾损伤(CSA-AKI)发生在20-30%的心脏手术合并体外循环(CPB)患者中。VA ECMO治疗的患者AKI发生率更高。CSA-AKI的发病机制尚不完全清楚,缺乏预防治疗。我们假设CSA-AKI的发生是由于泵相关的红细胞溶血和无细胞血红蛋白(CFH)和血凝素在肾脏的积累。方法:建立一种新的CPB心脏跳动模型。采用大鼠进行CPB实验;采用Millar有创血压导管测量血压(BP),采用fitc - sininistrin (FITC-S)法测定CPB后24 h肾小球滤过率(GFR)。Western免疫印迹法检测血凝素(Hpx)、谷胱甘肽过氧化物酶4 (GPX4)和β-肌动蛋白。采用ELISA法检测尿KIM-1。采用qRT-PCR法检测KIM-1和TATA-box Binding Protein 1 (TBP1) mRNA表达。ELISA法检测血浆游离血红蛋白(CFH)、Hpx、haptoglobin、IL-6水平。采用免疫荧光标记法检测肾脏中血红蛋白(Hb)、Hpx、meggalin和KIM-1。脂质过氧化用4-羟基壬烯醛(4-HNE)染色检测。结果:与假对照组相比,CPB后24小时GFR降低,肾组织切片评分较高,提示CPB所致AKI。CPB后尿KIM-1蛋白水平和肾KIM-1 mRNA水平升高。CPB后免疫荧光染色也显示管状KIM-1染色。CPB后血浆IL-6水平升高,CPB后24 h血浆Hpx升高。免疫荧光染色显示肾脏近端小管中Hpx和meggalin共定位,CPB后肾脏中有血红蛋白染色。最后,CPB诱导铁下垂,24 h时GPX4蛋白降低,4-HNE染色升高。重点。结论:CPB诱导AKI伴近端小管血红蛋白和Hpx沉积及铁下垂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Nephrology
American Journal of Nephrology 医学-泌尿学与肾脏学
CiteScore
7.50
自引率
2.40%
发文量
74
审稿时长
4-8 weeks
期刊介绍: The ''American Journal of Nephrology'' is a peer-reviewed journal that focuses on timely topics in both basic science and clinical research. Papers are divided into several sections, including:
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