TREML4 Promotes Inflammatory Programs in Human and Murine Macrophages and Alters Atherosclerosis Lesion Composition in the Apolipoprotein E Deficient Mouse

• Published in: Frontiers in immunology 2020-03, Vol.11, p.397
• Main Authors: Gonzalez-Cotto, Marieli, Guo, Liang, Karwan, Megan, Sen, Shurjo K, Barb, Jennifer, Collado, Carlos J, Elloumi, Fathi, Palmieri, Erika M, Boelte, Kimberly, Kolodgie, Frank D, Finn, Aloke V, Biesecker, Leslie G, McVicar, Daniel W
• Format: Article
• Language: English
• Subjects: Animals; Apolipoproteins E - deficiency; atherosclerosis; Atherosclerosis - immunology; Atherosclerosis - metabolism; Atherosclerosis - pathology; Cardiovascular Diseases - immunology; Cardiovascular Diseases - metabolism; Cardiovascular Diseases - pathology; Gene Expression Regulation - immunology; Humans; Immunology; inflammation; Inflammation - immunology; Inflammation - metabolism; Inflammation - pathology; macrophages; Macrophages - immunology; Macrophages - metabolism; Receptors, Immunologic - immunology; Receptors, Immunologic - metabolism; TREM family; treml4
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2020.00397

The Triggering Receptor Expressed on Myeloid cells-like 4 (TREML4) is a member of the TREM receptor family, known modulators of inflammatory responses. We have previously found that expression positively correlates with human coronary arterial calcification (CAC). However, the role of in the pathogenesis of cardiovascular disease remains incompletely defined. Since macrophages play a key role in inflammatory conditions, we investigated if activated macrophages selectively expressed and found that carriage of either one of the eQTL SNP's previously associated with increased expression conferred higher expression in human inflammatory macrophages (M1) compared to alternatively activated macrophages (M2). Furthermore, we found that expression in human M1 dysregulated several inflammatory pathways related to leukocyte activation, apoptosis and extracellular matrix degradation. Similarly, murine M1 expressed substantial levels of , as did oxLDL treated macrophages. Transcriptome analysis confirmed that murine controls the expression of genes related to inflammation and lipid regulation pathways, suggesting a possible role in atherosclerosis. Analysis of mice showed reduced plaque burden and lesion complexity as indicated by decreased stage scores, macrophage content and collagen deposition. Finally, transcriptome analysis of oxLDL-loaded murine macrophages showed that represses a specific set of genes related to carbohydrate, ion and amino acid membrane transport. Metabolomic analysis confirmed that deficiency may promote a beneficial relationship between iron homeostasis and glucose metabolism. Together, our results suggest that plays a role in the development of cardiovascular disease, as indicated by -dependent dysregulation of macrophage inflammatory pathways, macrophage metabolism and promotion of vulnerability features in advanced lesions.