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Male and female MLP\n                  <jats:sup>ko<\/jats:sup>\n                  mice received either vehicle or a mix of lipoxin-A\n                  <jats:sub>4<\/jats:sub>\n                  and lipoxin-B\n                  <jats:sub>4<\/jats:sub>\n                  three times per week for six weeks. Cardiac function was assessed using echocardiography, and fibrosis and DCM-associated cardiac signaling was evaluated through histology, immunofluorescence and immunoblot analyses. Flow cytometry and RNA sequencing (RNAseq) was performed to identify changes in cardiac gene expression and characterize macrophage subpopulations, respectively.\n                <\/jats:p>\n                <jats:p>\n                  Flow cytometry showed increased inflammatory CD11c\n                  <jats:sup>+<\/jats:sup>\n                  M1-like macrophages and reduction of CD206\n                  <jats:sup>+<\/jats:sup>\n                  M2-like macrophages in MLP\n                  <jats:sup>ko<\/jats:sup>\n                  hearts compared to wild-type controls. Lipoxin treatment partially reversed the macrophage imbalance and showed mild improvements in cardiac physiology in MLP\n                  <jats:sup>ko<\/jats:sup>\n                  males. RNAseq analyses revealed sex-dependent alterations in the expression of pro-fibrotic and inflammation-related genes, suggesting changes in extracellular matrix (ECM) integrity and composition, and to the adaptive immune response. Intriguingly, several ECM proteins showed unexpected localizations at cardiac intercalated disks, which are known to be involved in DCM etiology. Further analysis identified lipoxin-dependent reduction in the DCM-associated expression of intercalated disk components only in lipoxin-treated MLP\n                  <jats:sup>ko<\/jats:sup>\n                  males. Lipoxins also modulated key cardiac signaling pathways in a sex-specific manner, including Erk1\/2 and PKC\u03b1-linked Ankrd1\/Carp1, which is associated with DCM development in MLP\n                  <jats:sup>ko<\/jats:sup>\n                  mice. While lipoxins do not directly reverse cardiac dysfunction or fibrosis in MLP\n                  <jats:sup>ko<\/jats:sup>\n                  mice, they may provide sex-specific protective effects by modulating DCM-related cardiac signaling pathways and by influencing immune-cell populations.\n                <\/jats:p>","DOI":"10.64898\/2026.03.09.710477","type":"posted-content","created":{"date-parts":[[2026,3,11]],"date-time":"2026-03-11T13:35:13Z","timestamp":1773236113000},"source":"Crossref","is-referenced-by-count":0,"title":["Lipoxins Regulate Intercalated Disk-Associated Signaling and Immune Remodeling in Dilated Cardiomyopathy"],"prefix":"10.64898","author":[{"given":"Madison","family":"Clark","sequence":"first","affiliation":[{"name":"Department of Biomedicine, Aarhus University, Aarhus, Denmark and Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark"},{"name":"Division of Cardiology, School of Medicine, University of California San Diego, USA"},{"name":"Department of Clinical Immunology and Transfusion Medicine, Sahlgrenska University Hospital, Gothenburg, SE-40530, Sweden"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kyohei","family":"Fujita","sequence":"additional","affiliation":[{"name":"Division of Cardiology, School of Medicine, University of California San Diego, USA"},{"name":"Institute of Advanced Biomedical Engineering and Science, Tokyo Women\u2019s Medical University, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lena Anastasia Magdalena","family":"Nielsen","sequence":"additional","affiliation":[{"name":"Department of Biomedicine, Aarhus University, Aarhus, Denmark and Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert T.","family":"Johnson","sequence":"additional","affiliation":[{"name":"Department of Biomedicine, Aarhus University, Aarhus, Denmark and Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yusu","family":"Gu","sequence":"additional","affiliation":[{"name":"Division of Cardiology, School of Medicine, University of California San Diego, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nancy D.","family":"Dalton","sequence":"additional","affiliation":[{"name":"Division of Cardiology, School of Medicine, University of California San Diego, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bianca Esm\u00e9e","family":"Suur","sequence":"additional","affiliation":[{"name":"Department of Biomedicine, Aarhus University, Aarhus, Denmark and Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ida","family":"Bergstr\u00f6m","sequence":"additional","affiliation":[{"name":"Clinical Department of Clinical Immunology and Transfusion Medicine. 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