AUTHOR=Algoet Michiel , Wu Ming , Gillijns Hilde , Pusovnik Matic , Caluwe Ellen , Blazejczyk Kasia , Gsell Willy , Geerkens Lotte , De Groote Senne , Kuznetsova Tatiana , Himmelreich Uwe , Oosterlinck Wouter , Janssens Stefan 
  
TITLE=CLEC4E deletion in cardiac resident cells reduces infarct size and improves cardiac remodeling following myocardial ischemia-reperfusion injury
  
JOURNAL=Experimental Biology and Medicine
  
VOLUME=Volume 251 - 2026
  
YEAR=2026
  
URL=https://www.ebm-journal.org/journals/experimental-biology-and-medicine/articles/10.3389/ebm.2026.11196
  
DOI=10.3389/ebm.2026.11196
  
ISSN=1535-3699
  
ABSTRACT=The c-type lectin receptor CLEC4E plays a critical role in innate immune responses to ischemic tissue damage, and is expressed on infiltrating immune cells and tissue resident cells. We investigated whether inhibition of CLEC4E signaling in resident cells or infiltrating immune cells, mediates cardioprotection in myocardial ischemia-reperfusion (I/R) injury, and explored associated molecular pathways. Methods: We generated chimeric mice via sublethal total body irradiation followed by adoptive transfer of WT C57Bl6/J bone marrow cells (BMCs) in CLEC4E−/− mice and CLEC4E−/− BMCs in WT mice (n = 86). Four weeks after BMC transfer, we induced I/R injury by 30 min LAD occlusion. Myocardial necrosis was measured using troponin I (TnI) at 90 min; infarct size and LV remodeling were assessed by gadolinium-enhanced MRI at 24 h and 28 d. Hearts and bones were harvested at 28 d for immunohistochemistry, Olink-based myocardial proteomic analysis, and genotyping. Results: BMC analysis confirmed successful CLEC4E chimerism after transfer of CLEC4E−/− vs. WT progenitors. TnI levels and infarct size at 24 h were similar in both groups, but at 28 d, CLEC4E−/− mice with WT BMCs (n = 26) showed better LV function (LVEF 62% vs. 47%, p < 0.05) and smaller infarcts (6.9% vs. 19.8% LVmass, p < 0.01) than WT with CLEC4E−/− BMCs (n = 22). Proteomic analysis revealed enhanced pro-inflammatory and pro-fibrotic protein expression in WT with CLEC4E−/− BMCs. Conclusion: Deletion of CLEC4E in non–bone marrow–derived cardiac resident cells confers cardioprotection post-I/R. Targeting CLEC4E signaling and its downstream effectors in cardiac tissue may offer a novel therapeutic strategy for I/R injury.