<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>32(8)</volume><submitter>Zhao C</submitter><funding>National Natural Science Foundation of China</funding><pubmed_abstract>Vagus nerve regulates viral infection and inflammation via the alpha 7 nicotinic acetylcholine receptor (α7 nAChR); however, the role of α7 nAChR in ZIKA virus (ZIKV) infection, which can cause severe neurological diseases such as microcephaly and Guillain-Barré syndrome, remains unknown. Here, we first examined the role of α7 nAChR in ZIKV infection in vitro. A broad effect of α7 nAChR activation was identified in limiting ZIKV infection in multiple cell lines. Combined with transcriptomics analysis, we further demonstrated that α7 nAChR activation promoted autophagy and ferroptosis pathways to limit cellular ZIKV viral loads. Additionally, activation of α7 nAChR prevented ZIKV-induced p62 nucleus accumulation, which mediated an enhanced autophagy pathway. By regulating proteasome complex</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>2641-2661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11405161</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Activation of nicotinic acetylcholine receptor α7 subunit limits Zika viral infection via promoting autophagy and ferroptosis.</pubmed_title><pmcid>PMC11405161</pmcid><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Lin Z</pubmed_authors><pubmed_authors>Xie S</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors><pubmed_authors>Lai X</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Xu JF</pubmed_authors><pubmed_authors>Liang H</pubmed_authors><pubmed_authors>Zhao Q</pubmed_authors><pubmed_authors>Cheng L</pubmed_authors><pubmed_authors>Wu R</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Su X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Activation of nicotinic acetylcholine receptor α7 subunit limits Zika viral infection via promoting autophagy and ferroptosis.</name><description>Vagus nerve regulates viral infection and inflammation via the alpha 7 nicotinic acetylcholine receptor (α7 nAChR); however, the role of α7 nAChR in ZIKA virus (ZIKV) infection, which can cause severe neurological diseases such as microcephaly and Guillain-Barré syndrome, remains unknown. Here, we first examined the role of α7 nAChR in ZIKV infection in vitro. A broad effect of α7 nAChR activation was identified in limiting ZIKV infection in multiple cell lines. Combined with transcriptomics analysis, we further demonstrated that α7 nAChR activation promoted autophagy and ferroptosis pathways to limit cellular ZIKV viral loads. Additionally, activation of α7 nAChR prevented ZIKV-induced p62 nucleus accumulation, which mediated an enhanced autophagy pathway. By regulating proteasome complex</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-03-31T12:16:28.524Z</modification><creation>2025-09-01T03:08:27.01Z</creation></dates><accession>S-EPMC11405161</accession><cross_references><pubmed>38822526</pubmed><doi>10.1016/j.ymthe.2024.05.037</doi></cross_references></HashMap>