{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Huang Z"],"funding":["National Natural Science Foundation of China"],"pagination":["e17198"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10165355"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(5)"],"pubmed_abstract":["Atherosclerosis is a chronic inflammatory disease with high morbidity and mortality rates worldwide. Doublecortin-like kinase 1 (DCLK1), a microtubule-associated protein kinase, is involved in neurogenesis and human cancers. However, the role of DCLK1 in atherosclerosis remains undefined. In this study, we identified upregulated DCLK1 in macrophages in atherosclerotic lesions of ApoE<sup>-/-</sup> mice fed an HFD and determined that macrophage-specific DCLK1 deletion attenuates atherosclerosis by reducing inflammation in mice. Mechanistically, RNA sequencing analysis indicated that DCLK1 mediates oxLDL-induced inflammation via NF-κB signaling pathway in primary macrophages. Coimmunoprecipitation followed by LC-MS/MS analysis identified IKKβ as a binding protein of DCLK1. We confirmed that "],"journal":["EMBO molecular medicine"],"pubmed_title":["Macrophage DCLK1 promotes atherosclerosis via binding to IKKβ and inducing inflammatory responses."],"pmcid":["PMC10165355"],"funding_grant_id":["81930108","82000793","82170373","81970323"],"pubmed_authors":["Li W","Xu M","Liang G","Huang Z","Huang W","Luo W","Han X","Shen S","Wang Y","Wu G","Lin L"],"additional_accession":[]},"is_claimable":false,"name":"Macrophage DCLK1 promotes atherosclerosis via binding to IKKβ and inducing inflammatory responses.","description":"Atherosclerosis is a chronic inflammatory disease with high morbidity and mortality rates worldwide. Doublecortin-like kinase 1 (DCLK1), a microtubule-associated protein kinase, is involved in neurogenesis and human cancers. However, the role of DCLK1 in atherosclerosis remains undefined. In this study, we identified upregulated DCLK1 in macrophages in atherosclerotic lesions of ApoE<sup>-/-</sup> mice fed an HFD and determined that macrophage-specific DCLK1 deletion attenuates atherosclerosis by reducing inflammation in mice. Mechanistically, RNA sequencing analysis indicated that DCLK1 mediates oxLDL-induced inflammation via NF-κB signaling pathway in primary macrophages. Coimmunoprecipitation followed by LC-MS/MS analysis identified IKKβ as a binding protein of DCLK1. We confirmed that ","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2026-07-14T22:17:58.973Z","creation":"2025-04-05T10:55:06.106Z"},"accession":"S-EPMC10165355","cross_references":{"pubmed":["36896602"],"doi":["10.15252/emmm.202217198"]}}