Song He, Zhengbo Liao, Deyuan Tang, Zhiyong Zeng, Bin Wang, Piao Zhou, Yinming Mao, Wenwen Hu, Min Zhou
{"title":"PRV感染小鼠三叉神经节细胞后TLR3信号通路对I型干扰素分泌的调控","authors":"Song He, Zhengbo Liao, Deyuan Tang, Zhiyong Zeng, Bin Wang, Piao Zhou, Yinming Mao, Wenwen Hu, Min Zhou","doi":"10.1007/s11262-025-02146-2","DOIUrl":null,"url":null,"abstract":"<p><p>This study investigates the effects of pseudorabies virus (PRV) infection on the antiviral immune signaling pathway and type I interferon factors in mouse trigeminal ganglion (TG) cells. The experiment involved inoculating TG primary cells with PRV and intranasally infecting mice. The results indicated that PRV infection of mouse TG primary cells led to alterations in the gene and protein expression of TLR3, TRIF, TBK1, and IRF3, while inhibiting the expression of IκBα protein in the later stages of infection. Additionally, the phosphorylation of IRF3 and IκBα was induced both in vivo and in vitro. Following PRV infection, the expression of IFN-α was up-regulated in the supernatant, whereas its expression was down-regulated in the cell lysates and mouse TG. To further investigate the role of TLR3 in the IRF3 signaling pathway and type I interferon factors, siRNA was employed to interfere with TLR3 expression in TG cells. Western blot analysis was conducted to assess the expression of TLR3 signaling pathway-related proteins and the secretion of IFN-α following the interference. The findings demonstrated that siTLR3 effectively reduced TLR3 protein expression in TG cells and concurrently modulated the secretion of type I interferon factors via the TLR3-TRIF-TBK1-IRF3 signaling axis. Furthermore, PRV infection was shown to induce TLR3 expression in both mouse TG primary cells and mouse TG, thereby activating the TLR3-TRIF-TBK1-IRF3 signaling axis to regulate the antiviral immune response in TG cells, while simultaneously inhibiting IFN-α expression within TG cells and TG through the TLR3 signaling pathway. These experimental results elucidate the antiviral immune mechanism associated with the TLR3 signaling pathway following PRV infection of mouse TG cells, offering new insights into the immune evasion strategies employed by PRV.</p>","PeriodicalId":51212,"journal":{"name":"Virus Genes","volume":" ","pages":"574-587"},"PeriodicalIF":1.9000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulation of type I interferon factor secretion via the TLR3 signaling pathway after PRV infection of mouse trigeminal ganglion cells.\",\"authors\":\"Song He, Zhengbo Liao, Deyuan Tang, Zhiyong Zeng, Bin Wang, Piao Zhou, Yinming Mao, Wenwen Hu, Min Zhou\",\"doi\":\"10.1007/s11262-025-02146-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This study investigates the effects of pseudorabies virus (PRV) infection on the antiviral immune signaling pathway and type I interferon factors in mouse trigeminal ganglion (TG) cells. The experiment involved inoculating TG primary cells with PRV and intranasally infecting mice. The results indicated that PRV infection of mouse TG primary cells led to alterations in the gene and protein expression of TLR3, TRIF, TBK1, and IRF3, while inhibiting the expression of IκBα protein in the later stages of infection. Additionally, the phosphorylation of IRF3 and IκBα was induced both in vivo and in vitro. Following PRV infection, the expression of IFN-α was up-regulated in the supernatant, whereas its expression was down-regulated in the cell lysates and mouse TG. To further investigate the role of TLR3 in the IRF3 signaling pathway and type I interferon factors, siRNA was employed to interfere with TLR3 expression in TG cells. Western blot analysis was conducted to assess the expression of TLR3 signaling pathway-related proteins and the secretion of IFN-α following the interference. The findings demonstrated that siTLR3 effectively reduced TLR3 protein expression in TG cells and concurrently modulated the secretion of type I interferon factors via the TLR3-TRIF-TBK1-IRF3 signaling axis. Furthermore, PRV infection was shown to induce TLR3 expression in both mouse TG primary cells and mouse TG, thereby activating the TLR3-TRIF-TBK1-IRF3 signaling axis to regulate the antiviral immune response in TG cells, while simultaneously inhibiting IFN-α expression within TG cells and TG through the TLR3 signaling pathway. These experimental results elucidate the antiviral immune mechanism associated with the TLR3 signaling pathway following PRV infection of mouse TG cells, offering new insights into the immune evasion strategies employed by PRV.</p>\",\"PeriodicalId\":51212,\"journal\":{\"name\":\"Virus Genes\",\"volume\":\" \",\"pages\":\"574-587\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virus Genes\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11262-025-02146-2\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Genes","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11262-025-02146-2","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/5 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Regulation of type I interferon factor secretion via the TLR3 signaling pathway after PRV infection of mouse trigeminal ganglion cells.
This study investigates the effects of pseudorabies virus (PRV) infection on the antiviral immune signaling pathway and type I interferon factors in mouse trigeminal ganglion (TG) cells. The experiment involved inoculating TG primary cells with PRV and intranasally infecting mice. The results indicated that PRV infection of mouse TG primary cells led to alterations in the gene and protein expression of TLR3, TRIF, TBK1, and IRF3, while inhibiting the expression of IκBα protein in the later stages of infection. Additionally, the phosphorylation of IRF3 and IκBα was induced both in vivo and in vitro. Following PRV infection, the expression of IFN-α was up-regulated in the supernatant, whereas its expression was down-regulated in the cell lysates and mouse TG. To further investigate the role of TLR3 in the IRF3 signaling pathway and type I interferon factors, siRNA was employed to interfere with TLR3 expression in TG cells. Western blot analysis was conducted to assess the expression of TLR3 signaling pathway-related proteins and the secretion of IFN-α following the interference. The findings demonstrated that siTLR3 effectively reduced TLR3 protein expression in TG cells and concurrently modulated the secretion of type I interferon factors via the TLR3-TRIF-TBK1-IRF3 signaling axis. Furthermore, PRV infection was shown to induce TLR3 expression in both mouse TG primary cells and mouse TG, thereby activating the TLR3-TRIF-TBK1-IRF3 signaling axis to regulate the antiviral immune response in TG cells, while simultaneously inhibiting IFN-α expression within TG cells and TG through the TLR3 signaling pathway. These experimental results elucidate the antiviral immune mechanism associated with the TLR3 signaling pathway following PRV infection of mouse TG cells, offering new insights into the immune evasion strategies employed by PRV.
期刊介绍:
Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools.
Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments.
Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.