Lipid-associated macrophages transition to an inflammatory state in human atherosclerosis increasing the risk of cerebrovascular complications

在人类动脉粥样硬化中,脂质相关巨噬细胞会转变为炎症状态,从而增加脑血管并发症的风险。

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作者:Lea Dib # ,Lada A Koneva # ,Andreas Edsfeldt ,Yasemin-Xiomara Zurke ,Jiangming Sun ,Mihaela Nitulescu ,Moustafa Attar ,Esther Lutgens ,Steffen Schmidt ,Marie W Lindholm ,Robin P Choudhury ,Ismail Cassimjee ,Regent Lee ,Ashok Handa ,Isabel Goncalves ,Stephen N Sansom # ,Claudia Monaco #

Abstract

The immune system is integral to cardiovascular health and disease. Targeting inflammation ameliorates adverse cardiovascular outcomes. Atherosclerosis, a major underlying cause of cardiovascular disease (CVD), is conceptualised as a lipid-driven inflammation where macrophages play a non-redundant role. However, evidence emerging so far from single cell atlases suggests a dichotomy between lipid associated and inflammatory macrophage states. Here, we present an inclusive reference atlas of human intraplaque immune cell communities. Combining scRNASeq of human surgical carotid endarterectomies in a discovery cohort with bulk RNASeq and immunohistochemistry in a validation cohort (the Carotid Plaque Imaging Project-CPIP), we reveal the existence of PLIN2hi/TREM1hi macrophages as a toll-like receptor-dependent inflammatory lipid-associated macrophage state linked to cerebrovascular events. Our study shifts the current paradigm of lipid-driven inflammation by providing biological evidence for a pathogenic macrophage transition to an inflammatory lipid-associated phenotype and for its targeting as a new treatment strategy for CVD.

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