题名 | CircNr1h4 regulates the pathological process of renal injury in salt-sensitive hypertensive mice by targeting miR-155-5p |
作者 | |
发表日期 | 2020-01 |
发表期刊 | JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | circular RNAs hypertension miRNAs renal injury |
其他关键词 | ISCHEMIA-REPERFUSION INJURY ; CIRCULAR RNAS ; PROFILING REVEALS ; BLOOD-PRESSURE ; MICRORNA ; KIDNEY ; EXPRESSION ; DISEASE ; TRANSCRIPTOME ; DEFICIENCY |
摘要 | Circular RNAs are a class of widespread and diverse endogenous RNAs that may regulate gene expression in various diseases, but their regulation and function in hypertensive renal injury remain unclear. In this study, we generated ribosomal-depleted RNA sequencing data from normal mouse kidneys and from injured mouse kidneys induced by deoxycorticosterone acetate-salt hypertension and identified at least 4900 circRNA candidates. A total of 124 of these circRNAs were differentially expressed between the normal and injured kidneys. Furthermore, we characterized one abundant circRNA, termed circNr1h4, which is derived from the Nr1h4 gene and significantly down-regulated in the injured kidneys. RNA sequencing data and qPCR analysis also showed many microRNAs and mRNAs, including miR-155-5p and fatty acid reductase 1 (Far1), were differentially expressed between the normal and injured kidney and related to circNr1h4. In vitro, the silencing of circNr1h4 or overexpression of miR-155-5p significantly decreased Far1 levels and increased reactive oxygen species. Mechanistic investigations indicated that circNr1h4 acts as a competing endogenous RNA for miR-155-5p, leading to regulation of its target gene Far1. Our study provides novel insight into the molecular mechanisms underlying kidney injury in hypertension, which will be required to develop therapeutic strategies of targeting circRNAs for hypertensive kidney injury. |
资助项目 | Natural Science Foundation of Zhejiang ChinaNatural Science Foundation of Zhejiang Province [LY19H050001]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81670784] |
出版者 | WILEY |
出版地 | HOBOKEN |
ISSN | 1582-1838 |
EISSN | 1582-4934 |
卷号 | 24期号:2页码:1700-1712 |
DOI | 10.1111/jcmm.14863 |
页数 | 13 |
WOS类目 | Cell Biology ; Medicine, Research & Experimental |
WOS研究方向 | Cell Biology ; Research & Experimental Medicine |
WOS记录号 | WOS:000499147900001 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 31782248 |
PMC记录号 | PMC6991678 |
SCOPUSEID | 2-s2.0-85075714276 |
通讯作者地址 | [Weng, Huachun]Department of Clinical Research & Department of Pediatrics,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China |
Scopus学科分类 | Molecular Medicine;Cell Biology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/7450 |
专题 | 附属第一医院 药学院(分析测试中心)_药学系 |
通讯作者 | Weng, Huachun |
作者单位 | 1.Department of Clinical Research & Department of Pediatrics,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China; 2.Department of Pharmacy,Jinhua Central Hospital,Jinhua,China; 3.Department of Pharmaceutical Sciences,Wenzhou Medical University,Chashan University-town,Wenzhou,China; 4.Departments of Pediatrics,Pharmacology and Toxicology,Pediatric Research Institute,University of Louisville,Louisville,United States |
第一作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
通讯作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Lu, Chaosheng,Chen, Bicheng,Chen, Congcong,et al. CircNr1h4 regulates the pathological process of renal injury in salt-sensitive hypertensive mice by targeting miR-155-5p[J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE,2020,24(2):1700-1712. |
APA | Lu, Chaosheng., Chen, Bicheng., Chen, Congcong., Li, Haiyan., Wang, Dan., ... & Weng, Huachun. (2020). CircNr1h4 regulates the pathological process of renal injury in salt-sensitive hypertensive mice by targeting miR-155-5p. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 24(2), 1700-1712. |
MLA | Lu, Chaosheng,et al."CircNr1h4 regulates the pathological process of renal injury in salt-sensitive hypertensive mice by targeting miR-155-5p".JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 24.2(2020):1700-1712. |
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