<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li T</submitter><funding>Ministry of Science and Technology of China</funding><funding>Chinese Academy of Sciences</funding><funding>National Science and Technology Council Taiwan</funding><funding>Ministry of Education (MOE) in Taiwan</funding><funding>National Science Foundation of China</funding><pagination>RP87258</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11527428</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>Traumatic brain injury (TBI) caused by external mechanical forces is a major health burden worldwide, but the underlying mechanism in glia remains largely unclear. We report herein that &lt;i>Drosophila&lt;/i> adults exhibit a defective blood-brain barrier, elevated innate immune responses, and astrocyte swelling upon consecutive strikes with a high-impact trauma device. RNA sequencing (RNA-seq) analysis of these astrocytes revealed upregulated expression of genes encoding PDGF and VEGF receptor-related (Pvr, a receptor tyrosine kinase), adaptor protein complex 1 (AP-1&lt;i>,&lt;/i> a transcription factor complex of the c-Jun N-terminal kinase pathway) composed of Jun-related antigen (Jra) and kayak (kay), and matrix metalloproteinase 1 (Mmp1) following TBI. Interestingly, Pvr is both required and suf</pubmed_abstract><journal>eLife</journal><pubmed_title>A Pvr-AP-1-Mmp1 signaling pathway is activated in astrocytes upon traumatic brain injury.</pubmed_title><pmcid>PMC11527428</pmcid><funding_grant_id>31921002</funding_grant_id><funding_grant_id>32170962</funding_grant_id><funding_grant_id>2021ZD0203900</funding_grant_id><funding_grant_id>113-2628-B-A49-007</funding_grant_id><funding_grant_id>2019YFA0707100</funding_grant_id><funding_grant_id>31861143031</funding_grant_id><funding_grant_id>Higher Education Sprout Project</funding_grant_id><funding_grant_id>31830036</funding_grant_id><funding_grant_id>Strategic Priority Research Program B XDBS1020100</funding_grant_id><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Ho MS</pubmed_authors><pubmed_authors>Shi W</pubmed_authors><pubmed_authors>Zhang YQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Pvr-AP-1-Mmp1 signaling pathway is activated in astrocytes upon traumatic brain injury.</name><description>Traumatic brain injury (TBI) caused by external mechanical forces is a major health burden worldwide, but the underlying mechanism in glia remains largely unclear. We report herein that &lt;i>Drosophila&lt;/i> adults exhibit a defective blood-brain barrier, elevated innate immune responses, and astrocyte swelling upon consecutive strikes with a high-impact trauma device. RNA sequencing (RNA-seq) analysis of these astrocytes revealed upregulated expression of genes encoding PDGF and VEGF receptor-related (Pvr, a receptor tyrosine kinase), adaptor protein complex 1 (AP-1&lt;i>,&lt;/i> a transcription factor complex of the c-Jun N-terminal kinase pathway) composed of Jun-related antigen (Jra) and kayak (kay), and matrix metalloproteinase 1 (Mmp1) following TBI. Interestingly, Pvr is both required and suf</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-05T09:12:34.313Z</modification><creation>2025-04-05T09:12:34.313Z</creation></dates><accession>S-EPMC11527428</accession><cross_references><pubmed>39480704</pubmed><doi>10.7554/eLife.87258</doi></cross_references></HashMap>