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新冠病毒相关枢纽基因在肝脏生理和病理再生中的探索与验证

Exploration and verification of COVID-19-related hub genes in liver physiological and pathological regeneration.

作者信息

Shi Jihang, Li Guangya, Yuan Xiandun, Wang Yafei, Gong Ming, Li Chonghui, Ge Xinlan, Lu Shichun

机构信息

Medical School of Chinese People's Liberation Army (PLA), Beijing, China.

Faculty of Hepato-Pancreato-Biliary Surgery, Chinese PLA General Hospital, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2023 Feb 23;11:1135997. doi: 10.3389/fbioe.2023.1135997. eCollection 2023.

Abstract

An acute injury is often accompanied by tissue regeneration. In this process, epithelial cells show a tendency of cell proliferation under the induction of injury stress, inflammatory factors, and other factors, accompanied by a temporary decline of cellular function. Regulating this regenerative process and avoiding chronic injury is a concern of regenerative medicine. The severe coronavirus disease 2019 (COVID-19) has posed a significant threat to people's health caused by the coronavirus. Acute liver failure (ALF) is a clinical syndrome resulting from rapid liver dysfunction with a fatal outcome. We hope to analyze the two diseases together to find a way for acute failure treatment. COVID-19 dataset (GSE180226) and ALF dataset (GSE38941) were downloaded from the Gene Expression Omnibus (GEO) database, and the "Deseq2" package and "limma" package were used to identify differentially expressed genes (DEGs). Common DEGs were used for hub genes exploration, Protein-Protein Interaction (PPI) network construction, Gene Ontology (GO) functional enrichment, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment. The real-time reverse transcriptase-polymerase chain reaction (RT-qPCR) was used to verify the role of hub genes in liver regeneration during expansion of liver cells and a CCl4-induced ALF mice model. The common gene analysis of the COVID-19 and ALF databases revealed 15 hub genes from 418 common DEGs. These hub genes, including CDC20, were related to cell proliferation and mitosis regulation, reflecting the consistent tissue regeneration change after the injury. Furthermore, hub genes were verified expansion of liver cells and ALF model. On this basis, the potential therapeutic small molecule of ALF was found by targeting the hub gene CDC20. We have identified hub genes for epithelial cell regeneration under acute injury conditions and explored a new small molecule Apcin for liver function maintenance and ALF treatment. These findings may provide new approaches and ideas for treating COVID-19 patients with ALF.

摘要

急性损伤常伴有组织再生。在此过程中,上皮细胞在损伤应激、炎症因子等因素的诱导下呈现细胞增殖趋势,同时细胞功能暂时下降。调控这一再生过程并避免慢性损伤是再生医学关注的问题。2019年严重冠状病毒病(COVID-19)由冠状病毒引起,对人们的健康构成了重大威胁。急性肝衰竭(ALF)是一种因肝脏功能迅速衰竭导致致命后果的临床综合征。我们希望将这两种疾病放在一起分析,以找到急性衰竭的治疗方法。从基因表达综合数据库(GEO)下载了COVID-19数据集(GSE180226)和ALF数据集(GSE38941),并使用“Deseq2”软件包和“limma”软件包来识别差异表达基因(DEG)。利用共同的DEG进行枢纽基因探索、蛋白质-蛋白质相互作用(PPI)网络构建、基因本体论(GO)功能富集和京都基因与基因组百科全书(KEGG)通路富集。采用实时逆转录-聚合酶链反应(RT-qPCR)验证枢纽基因在肝细胞扩增和四氯化碳诱导的ALF小鼠模型肝脏再生过程中的作用。对COVID-19和ALF数据库的共同基因分析从418个共同DEG中揭示了15个枢纽基因。这些枢纽基因,包括细胞分裂周期蛋白20(CDC20),与细胞增殖和有丝分裂调控有关,反映了损伤后一致的组织再生变化。此外,在肝细胞扩增和ALF模型中对枢纽基因进行了验证。在此基础上,通过靶向枢纽基因CDC20发现了ALF潜在的治疗性小分子。我们确定了急性损伤条件下上皮细胞再生的枢纽基因,并探索了一种用于维持肝功能和治疗ALF的新型小分子Apcin。这些发现可能为治疗合并ALF的COVID-19患者提供新的方法和思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc3/9997844/c2f2a4967a7a/fbioe-11-1135997-g001.jpg

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