Elabela alleviates ferroptosis, myocardial remodeling, fibrosis and heart dysfunction in hypertensive mice by modulating the IL-6/STAT3/GPX4 signaling

纤维化 心肌纤维化 血管紧张素II 下调和上调 心脏纤维化 内科学 炎症 内分泌学 医学 氧化应激 基因敲除 伊诺斯 受体 化学 细胞凋亡 一氧化氮 一氧化氮合酶 生物化学 基因
作者
Zhenzhou Zhang,Jianqiong Tang,Jiawei Song,Mengshi Xie,Ying Liu,Zhaojie Dong,Xiaoyan Liu,Xueting Li,Mi-Wen Zhang,Yihang Chen,Hongyu Shi,Jiuchang Zhong
出处
期刊:Free Radical Biology and Medicine [Elsevier]
卷期号:181: 130-142 被引量:125
标识
DOI:10.1016/j.freeradbiomed.2022.01.020
摘要

Hypertension-mediated pathological cardiac remodeling often progresses to heart failure. Elabela, mainly expressed in the cardiac microvascular endothelial cells (CMVECs), functions as a new endogenous ligand for apelin receptor. However, the exact roles of elabela in hypertension remain largely unclear. In this study, 10-week-old male C57BL/6 mice were randomly subjected to infusion of angiotensin (Ang) II (1.5 mg/kg/d) or saline for 2 weeks. Ang II infusion led to marked increases in systolic blood pressure levels and reduction of elabela levels in hypertensive mice with augmented myocardial hypertrophy and fibrosis. Furthermore, administration of elabela or ferroptosis inhibitor ferrostatin-1 significantly prevented Ang II-mediated pathological myocardial remodeling, dysfunction, and ultrastructural injury in hypertensive mice with downregulated expression of inflammation-, hypertrophy-, and fibrosis-related genes. Notably, elabela strikingly alleviated Ang II-induced upregulation of iron levels and lipid peroxidation in hypertensive mice by suppressing cardiac interleukin-6 (IL-6)/STAT3 signaling and activating the xCT/glutathione peroxidase (GPX4) signaling. In cultured CMVECs, exposure to Ang II resulted in a marked decrease in elabela levels and obvious increases in cellular ferroptosis, proliferation, inflammation, and superoxide production, which were rescued by elabela or ferrostatin-1 while were blocked by co-treatment with rhIL-6. Furthermore, knockdown of elabela by siRNA in CMVECs contributed to Ang II-mediated augmentations in cellular proliferation, migration, and oxidative stress in cultured cardiac fibroblasts and cardiomyocytes, respectively. In conclusion, elabela antagonizes Ang II-mediated promotion of CMVECs ferroptosis, adverse myocardial remodeling, fibrosis and heart dysfunction through modulating the IL-6/STAT3/GPX4 signaling pathway. Targeting elabela-APJ axis serves as a novel strategy for hypertensive heart diseases.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
田様应助科研通管家采纳,获得10
刚刚
傅双庆应助科研通管家采纳,获得20
刚刚
汉堡包应助科研通管家采纳,获得10
刚刚
情怀应助科研通管家采纳,获得10
刚刚
科目三应助科研通管家采纳,获得10
刚刚
机灵柚子应助科研通管家采纳,获得10
刚刚
1秒前
981678发布了新的文献求助10
4秒前
重要板凳发布了新的文献求助10
14秒前
一定能成功!完成签到,获得积分10
18秒前
樹里完成签到,获得积分10
19秒前
风趣的初阳完成签到 ,获得积分20
21秒前
23秒前
yuze_22发布了新的文献求助10
25秒前
27秒前
欣喜念梦完成签到,获得积分10
27秒前
lishui发布了新的文献求助10
27秒前
wbgwudi完成签到,获得积分10
30秒前
小小波吉完成签到,获得积分10
36秒前
38秒前
清爽匪完成签到,获得积分10
38秒前
kele完成签到 ,获得积分10
41秒前
谷粱紫槐完成签到,获得积分10
42秒前
怕黑行恶发布了新的文献求助10
42秒前
aaaabc完成签到 ,获得积分10
44秒前
wmuer完成签到 ,获得积分10
47秒前
可爱的函函应助511采纳,获得10
49秒前
50秒前
谷粱紫槐发布了新的文献求助10
50秒前
50秒前
小稻草人应助怕黑行恶采纳,获得10
50秒前
JHGG应助Albert采纳,获得10
53秒前
57秒前
57秒前
怕黑行恶完成签到,获得积分10
58秒前
bbb完成签到 ,获得积分10
1分钟前
在水一方应助微凉采纳,获得10
1分钟前
赘婿应助小小波吉采纳,获得10
1分钟前
打打应助fxx采纳,获得10
1分钟前
lgl发布了新的文献求助10
1分钟前
高分求助中
LNG地下式貯槽指針(JGA指-107) 1000
LNG地上式貯槽指針 (JGA指 ; 108) 1000
Preparation and Characterization of Five Amino-Modified Hyper-Crosslinked Polymers and Performance Evaluation for Aged Transformer Oil Reclamation 700
Operative Techniques in Pediatric Orthopaedic Surgery 510
How Stories Change Us A Developmental Science of Stories from Fiction and Real Life 500
九经直音韵母研究 500
Full waveform acoustic data processing 500
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2930127
求助须知:如何正确求助?哪些是违规求助? 2581791
关于积分的说明 6962974
捐赠科研通 2230389
什么是DOI,文献DOI怎么找? 1184998
版权声明 589575
科研通“疑难数据库(出版商)”最低求助积分说明 580095