VEGF抑制剂治疗不同缺氧程度大鼠肾脏后微小RNA表达的分析。

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Physiological genomics Pub Date : 2023-11-01 Epub Date: 2023-08-29 DOI:10.1152/physiolgenomics.00023.2023
Yaya Xu, Yueniu Zhu, Jiayue Xu, Haoyun Mao, Jiru Li, Xiaodong Zhu, Xiangmei Kong, Jianhua Zhang
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引用次数: 0

摘要

此前,我们发现慢性缺氧患者肾损伤的发生率与动脉氧分压有关。然而,在导致肾损伤的氧浓度下,微小RNA(miRNA)和缺氧诱导因子-1α(HIF-1α)-血管内皮生长因子(VEGF)轴之间的关系变化以及参与这一过程的关键miRNA尚未阐明。因此,我们阐明了不同氧浓度下VEGF与肾损伤之间的关系以及miRNA介导的机制。Sprague-Dawley大鼠暴露于常压缺氧,并根据吸入的氧气浓度和注射血管生成抑制剂贝伐单抗(一种人源化抗VEGF单克隆抗体)分为六组。对肾组织样本进行处理,以确定病理和形态学变化以及HIF-1α、VEGF和miRNA的表达。我们对高危途径和关键枢纽基因进行了聚类分析。使用两个基因表达综合数据集(GSE94717和GSE30718)验证了结果。随着吸入氧气浓度的降低,肾组织的破坏性变化变得更加严重。尽管肾脏在中等程度的缺氧(10%O2)下具有自我保护机制,但贝伐单抗注射破坏了这种机制,VEGF的表达与肾脏自我修复的能力有关。rno-miR-124-3p被鉴定为一种重要的miRNA;在这个过程中,一个关键的基因靶点Mapk14被鉴定出来。VEGF在不同缺氧水平下保护肾脏免受损伤中起着重要作用。特异性miRNA及其靶基因可能作为生物标志物,为肾损伤治疗提供新的见解。新的和值得注意的是,肾脏对缺氧环境的耐受性是有限的,缺氧程度与血管生成没有线性关系。VEGF在不同缺氧水平下肾脏的自我保护机制中起着重要作用。miR-124-3p在肾脏修复中可能特别重要,并且它可以通过miR-124-3p/Mapk14信号通路调节VEGF的表达。这些微小RNA可以作为生物标志物,为肾损伤治疗提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of microRNA expression in rat kidneys after VEGF inhibitor treatment under different degrees of hypoxia.

Previously, we found that the incidence of kidney injury in patients with chronic hypoxia was related to the partial pressure of arterial oxygen. However, at oxygen concentrations that contribute to kidney injury, the changes in the relationship between microRNAs (miRNAs) and the hypoxia-inducible factor-1α (HIF-1α)-vascular endothelial growth factor (VEGF) axis and the key miRNAs involved in this process have not been elucidated. Therefore, we elucidated the relationship between VEGF and kidney injury at different oxygen concentrations and the mechanisms mediated by miRNAs. Sprague-Dawley rats were exposed to normobaric hypoxia and categorized into six groups based on the concentration of the oxygen inhaled and injection of the angiogenesis inhibitor bevacizumab, a humanized anti-VEGF monoclonal antibody. Renal tissue samples were processed to determine pathological and morphological changes and HIF-1α, VEGF, and miRNA expression. We performed a clustering analysis of high-risk pathways and key hub genes. The results were validated using two Gene Expression Omnibus datasets (GSE94717 and GSE30718). As inhaled oxygen concentration decreased, destructive changes in the kidney tissues became more severe. Although the kidney possesses a self-protective mechanism under an intermediate degree of hypoxia (10% O2), bevacizumab injections disrupted this mechanism, and VEGF expression was associated with the ability of the kidney to repair itself. rno-miR-124-3p was identified as a crucial miRNA; a key gene target, Mapk14, was identified during this process. VEGF plays an important role in kidney protection from injury under different hypoxia levels. Specific miRNAs and their target genes may serve as biomarkers that provide new insights into kidney injury treatment.NEW & NOTEWORTHY Renal tolerance to hypoxic environments is limited, and the degree of hypoxia does not show a linear relationship with angiogenesis. VEGF plays an important role in the kidney's self-protective mechanism under different levels of hypoxia. miR-124-3p may be particularly important in kidney repair, and it may modulate VEGF expression through the miR-124-3p/Mapk14 signaling pathway. These microRNAs may serve as biomarkers that provide new insights into kidney injury treatment.

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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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