Identification of autophagy-associated circRNAs in sepsis-induced cardiomyopathy of mice

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作者
Ming-zhi Zheng
Jun-sheng Lou
Yun-peng Fan
Chun-yan Fu
Xing-jia Mao
Xiang Li
Kai Zhong
Lin-huizi Lu
Lin-lin Wang
Ying-ying Chen
Liang-rong Zheng
机构
[1] Zhejiang University,Department of Cardiology and Atrial Fibrillation Center, The First Affiliated Hospital, School of Medicine
[2] Hangzhou Medical College,Department of Pharmacology
[3] Zhejiang University School of Medicine,Department of Orthopedic Surgery, The First Affiliated Hospital
[4] Zhejiang University School of Medicine,Department of Basic Medicine Sciences, and Department of Obstetrics of the Second Affiliated Hospital
[5] Zhejiang University School of Medicine,Department of Basic Medicine Sciences, and Department of Orthopaedics of Sir Run Run Shaw Hospital
[6] Hangzhou Medical College,Department of Clinical Medicine
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摘要
Circular RNAs (circRNAs) play a role in sepsis-related autophagy. However, the role of circRNAs in autophagy after sepsis-induced cardiomyopathy (SICM) is unknown, so we explored the circRNA expression profiles associated with autophagy in an acute sepsis mouse model. At a dose of 10 mg/kg, mice were intraperitoneally administered with lipopolysaccharides. The myocardial tissue was harvested after 6 h for microarray analysis, qRT-PCR, and western blotting. Gene Ontology, Kyoto Encyclopedia of Genes and Genomes and Gene Set Enrichment Analysis were evaluated, and a competing endogenous RNA network was constructed, to evaluate the role of circRNAs related to autophagy in SICM. In total, 1,735 differently expressed circRNAs were identified in the LPS-treated group, including 990 upregulated and 745 downregulated circRNAs. The expression level of the autophagy-specific protein p62 decreased, while the ratio of LC3 II to LC3 I increased. Additionally, 309 mRNAs and 187 circRNAs were correlated with autophagy in myocardial tissue after SICM. Of these, 179 circRNAs were predicted to function as “miRNA sponges”. Some distinctive circRNAs and mRNAs found by ceRNA analysis might be involved in autophagy in SICM. These findings provide insights into circRNAs and identified new research targets that may be used to further explore the pathogenesis of SICM.
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