<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yi H</submitter><funding>Natural Science Foundation of Jilin Province</funding><pagination>e70048</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12484710</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(4)</volume><pubmed_abstract>Abdominal aortic aneurysm (AAA) is a life-threatening vascular disorder lacking effective pharmacological interventions. We identified CD5 molecule-like (CD5L) as a regulator of macrophage polarization in AAA via the phosphoinositide 3-kinase/protein kinase B/nuclear factor kappa B (PI3K/Akt/NF-κB) pathway. Transcriptomic analyses (GSE47472 and GSE57691) and angiotensin II (AngII)-infused apolipoprotein E-deficient (ApoE&lt;sup>-/-&lt;/sup>) mice showed CD5L upregulation, inversely correlated with M1 macrophage infiltration. In vitro CD5L overexpression reduced, whereas knockdown increased M1 polarization and pro-inflammatory cytokines in RAW264.7 cells and human monocyte-derived macrophages. In vivo, CD5L knockdown aggravated aortic dilation, vascular disruption, and inflammatory mediator expre</pubmed_abstract><journal>Journal of cell communication and signaling</journal><pubmed_title>Targeting the PI3K/Akt/NF-κB axis: Cluster of differentiation 5-like-mediated immunometabolic regulation of macrophage polarization in abdominal aortic aneurysm.</pubmed_title><pmcid>PMC12484710</pmcid><funding_grant_id>20230203582JC</funding_grant_id><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Yi H</pubmed_authors><pubmed_authors>Duan M</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Liu N</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wan T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting the PI3K/Akt/NF-κB axis: Cluster of differentiation 5-like-mediated immunometabolic regulation of macrophage polarization in abdominal aortic aneurysm.</name><description>Abdominal aortic aneurysm (AAA) is a life-threatening vascular disorder lacking effective pharmacological interventions. We identified CD5 molecule-like (CD5L) as a regulator of macrophage polarization in AAA via the phosphoinositide 3-kinase/protein kinase B/nuclear factor kappa B (PI3K/Akt/NF-κB) pathway. Transcriptomic analyses (GSE47472 and GSE57691) and angiotensin II (AngII)-infused apolipoprotein E-deficient (ApoE&lt;sup>-/-&lt;/sup>) mice showed CD5L upregulation, inversely correlated with M1 macrophage infiltration. In vitro CD5L overexpression reduced, whereas knockdown increased M1 polarization and pro-inflammatory cytokines in RAW264.7 cells and human monocyte-derived macrophages. In vivo, CD5L knockdown aggravated aortic dilation, vascular disruption, and inflammatory mediator expre</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-04T02:28:08.966Z</modification><creation>2026-05-04T03:13:28.132Z</creation></dates><accession>S-EPMC12484710</accession><cross_references><pubmed>41040887</pubmed><doi>10.1002/ccs3.70048</doi></cross_references></HashMap>