Liyuan Zhang , Tingting Huang , Hongjie He , Fuyi Xu , Chunhua Yang , Lu Lu , Geng Tian , Lei Wang , Jia Mi
{"title":"通过系统遗传学方法揭示Ace2-介导的COVID-19后认知功能障碍的分子机制。","authors":"Liyuan Zhang , Tingting Huang , Hongjie He , Fuyi Xu , Chunhua Yang , Lu Lu , Geng Tian , Lei Wang , Jia Mi","doi":"10.1016/j.expneurol.2024.114921","DOIUrl":null,"url":null,"abstract":"<div><p>The dysregulation of Angiotensin-converting enzyme 2 (ACE2) in central nervous system is believed associates with COVID-19 induced cognitive dysfunction. However, the detailed mechanism remains largely unknown. In this study, we performed a comprehensive system genetics analysis on hippocampal <em>ACE2</em> based on BXD mice panel. Expression quantitative trait loci (eQTLs) mapping showed that <em>Ace2</em> was strongly trans-regulated, and the elevation of <em>Ace2</em> expression level was significantly correlated with impaired cognitive functions. Further Gene co-expression analysis showed that <em>Ace2</em> may be correlated with the membrane proteins in Calcium signaling pathway. Further, qRT-PCR confirmed that SARS-CoV-2 spike S1 protein upregulated <em>ACE2</em> expression together with eight membrane proteins in Calcium Signaling pathway. Moreover, such elevation can be attenuated by recombinant <em>ACE2</em>. Collectively, our findings revealed a potential mechanism of <em>Ace2</em> in cognitive dysfunction, which could be beneficial for COVID–19–induced cognitive dysfunction prevention and potential treatment.</p></div>","PeriodicalId":12246,"journal":{"name":"Experimental Neurology","volume":"381 ","pages":"Article 114921"},"PeriodicalIF":4.6000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unraveling the molecular mechanisms of Ace2-mediated post-COVID-19 cognitive dysfunction through systems genetics approach\",\"authors\":\"Liyuan Zhang , Tingting Huang , Hongjie He , Fuyi Xu , Chunhua Yang , Lu Lu , Geng Tian , Lei Wang , Jia Mi\",\"doi\":\"10.1016/j.expneurol.2024.114921\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The dysregulation of Angiotensin-converting enzyme 2 (ACE2) in central nervous system is believed associates with COVID-19 induced cognitive dysfunction. However, the detailed mechanism remains largely unknown. In this study, we performed a comprehensive system genetics analysis on hippocampal <em>ACE2</em> based on BXD mice panel. Expression quantitative trait loci (eQTLs) mapping showed that <em>Ace2</em> was strongly trans-regulated, and the elevation of <em>Ace2</em> expression level was significantly correlated with impaired cognitive functions. Further Gene co-expression analysis showed that <em>Ace2</em> may be correlated with the membrane proteins in Calcium signaling pathway. Further, qRT-PCR confirmed that SARS-CoV-2 spike S1 protein upregulated <em>ACE2</em> expression together with eight membrane proteins in Calcium Signaling pathway. Moreover, such elevation can be attenuated by recombinant <em>ACE2</em>. Collectively, our findings revealed a potential mechanism of <em>Ace2</em> in cognitive dysfunction, which could be beneficial for COVID–19–induced cognitive dysfunction prevention and potential treatment.</p></div>\",\"PeriodicalId\":12246,\"journal\":{\"name\":\"Experimental Neurology\",\"volume\":\"381 \",\"pages\":\"Article 114921\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Experimental Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014488624002474\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Neurology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014488624002474","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Unraveling the molecular mechanisms of Ace2-mediated post-COVID-19 cognitive dysfunction through systems genetics approach
The dysregulation of Angiotensin-converting enzyme 2 (ACE2) in central nervous system is believed associates with COVID-19 induced cognitive dysfunction. However, the detailed mechanism remains largely unknown. In this study, we performed a comprehensive system genetics analysis on hippocampal ACE2 based on BXD mice panel. Expression quantitative trait loci (eQTLs) mapping showed that Ace2 was strongly trans-regulated, and the elevation of Ace2 expression level was significantly correlated with impaired cognitive functions. Further Gene co-expression analysis showed that Ace2 may be correlated with the membrane proteins in Calcium signaling pathway. Further, qRT-PCR confirmed that SARS-CoV-2 spike S1 protein upregulated ACE2 expression together with eight membrane proteins in Calcium Signaling pathway. Moreover, such elevation can be attenuated by recombinant ACE2. Collectively, our findings revealed a potential mechanism of Ace2 in cognitive dysfunction, which could be beneficial for COVID–19–induced cognitive dysfunction prevention and potential treatment.
期刊介绍:
Experimental Neurology, a Journal of Neuroscience Research, publishes original research in neuroscience with a particular emphasis on novel findings in neural development, regeneration, plasticity and transplantation. The journal has focused on research concerning basic mechanisms underlying neurological disorders.