GAS5 promotes glucose metabolism reprogramming and resistance to ferroptosis of endothelial progenitor cells through the miR-495-3p/SIX1 and IGF2BP2/NRF2 dual-regulatory pathways in coronary heart disease.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ming Zhong, Wenxia Xu, Biao Tang, Qiang Zhao, Zenan Jiang, Yinfeng Liu
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引用次数: 0

Abstract

We aimed to explore the potential along with mechanism of lncRNA growth arrest-specific 5 (GAS5) in modulating glucose metabolism and ferroptosis of endothelial progenitor cells (EPCs) in coronary heart disease (CHD). CCK-8, flow cytometry, EdU, colony formation, scratch test as well as transwell assays were implemented to assess cell biological behaviors. Glucose uptake testing, lactic acid production assay, and detection of extracellular acidification rate (EACR) together with oxygen consumption rate (OCR) were used to assess glucose metabolism. Iron, GSH and MDA detection were used to measure ferroptosis. Besides, a series of mechanical experiments were implemented to clarify the modulatory relationship between GAS5 and nuclear factor erythroid 2-related factor 2 (NRF2) as well as sine oculis homeobox 1 (SIX1). We found that GAS5 was down-regulated in CHD patients relative to healthy controls. GAS5 depletion repressed EPCs proliferation, migration along with invasion while elevated cell apoptosis. GAS5 promoted the reprogramming of glucose metabolism and inhibited ferroptosis in EPCs. GAS5 affected glycometabolic reprogramming and ferroptosis resistance through regulating SIX1 and NRF2. On the one hand, GAS5 promoted NRF2 mRNA stability through IGF2BP2. On the other hand, GAS5 regulated the miR-495-3p/SIX1 axis in EPCs. To sum up, GAS5 promotes glucose metabolism reprogramming and resistance to ferroptosis of EPCs through the miR-495-3p/SIX1 and IGF2BP2/NRF2 dual-regulatory pathways in CHD.

GAS5通过miR-495-3p/SIX1和IGF2BP2/NRF2双调控途径促进冠心病内皮祖细胞的糖代谢重编程和抗铁细胞沉积。
我们的目的是探索lncRNA生长停滞特异性5(GAS5)在冠心病(CHD)中调节内皮祖细胞(EPCs)糖代谢和铁变态反应的潜力和机制。研究人员采用了 CCK-8、流式细胞术、EdU、集落形成、划痕试验以及透孔试验来评估细胞生物学行为。葡萄糖摄取试验、乳酸生成试验、细胞外酸化率(EACR)和耗氧量(OCR)检测用于评估葡萄糖代谢。铁、GSH 和 MDA 检测用于测量铁变态反应。此外,还进行了一系列机械实验,以明确GAS5与核因子红细胞2相关因子2(NRF2)以及正弦眼同源框1(SIX1)之间的调节关系。我们发现,相对于健康对照组,GAS5在CHD患者中下调。GAS5消耗抑制了EPCs的增殖、迁移和侵袭,同时增加了细胞凋亡。GAS5促进了葡萄糖代谢的重编程,并抑制了EPCs的铁变态反应。GAS5 通过调控 SIX1 和 NRF2 影响糖代谢重编程和铁变态反应抵抗。一方面,GAS5 通过 IGF2BP2 促进 NRF2 mRNA 的稳定性。另一方面,GAS5 调节了 EPCs 中的 miR-495-3p/SIX1 轴。综上所述,GAS5通过miR-495-3p/SIX1和IGF2BP2/NRF2双调控途径促进了CHD患者EPCs的糖代谢重编程和抗铁蛋白沉积。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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