Innate immunity in atherosclerosis : the role of pattern recognition receptors

Sammanfattning: The pathogenesis of atherosclerosis is greatly influenced by the activities of both innate and adaptive immunity. Danger signals such as cholesterol crystals, oxidized LDL, and modified phospholipids may trigger sterile inflammation in atherosclerosis. Systemic infection or transient release of pathogen associated molecules in the circulation might also activate immune system and affect atherosclerosis. Activation of the innate immunity relies on a set of pattern recognition receptors (PRRs). Thus, PRRs are fundamental for activating the innate immunity in atherosclerosis. This thesis focuses on the role of three different PRRs in atherosclerosis, including NOD1, NOD2 and TLR9. We hypothesized that these PRRs regulate immune responses in the pathogenesis of atherosclerosis. We found that NOD2 is expressed in endothelial cells and macrophages in atherosclerotic plaques, and lesional NOD2 signal leads to activation of PGE2 pathway via NF-kB and MAPK p38. NOD2 activation in vivo promotes the development of vulnerable atherosclerotic plaques, characterized by enlarged necrotic core in the atherosclerotic plaques and enhanced vascular inflammation. Furthermore, NOD2 induces lipid retention in macrophages may contribute to the necrotic core formation. Although belonging to the same family, NOD1 signal promotes another lesional phenotype characterized by occlusive atherosclerosis with elastin degradation and vascular smooth muscle cell (VSMC) activation. In vitro stimulation of SMCs with NOD1 ligand induces chemokine and MMP production as well as enhances migration ability. Our data point to a possible mechanism via NOD1 in the development of occlusive atherosclerotic lesions. Unlike NOD1 and NOD2, TLR9 stimulation decreases atherosclerosis and necrotic core albeit activates local and systemic inflammation. Two important anti-inflammatory mediators IL-10 and IDO are induced by TLR9 activation and are potential contributors to the mechanisms that TLR9 restrains atherosclerosis. In summary, we identified three innate immune pathways linked to the distinct features of atherosclerosis. NOD2 leads to formation of vulnerable plaques with big necrotic cores. NOD1 promotes severe occlusive atherosclerosis. TLR9 signal restrains the development of atherosclerosis.