Department of Cardiovascular Medicine, State Key Laboratory of Medical Genomics, Shanghai Key Laboratory of Hypertension, Shanghai Institute of Hypertension, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Physiology and Pathophysiology, Shanghai Key Laboratory of Bioactive Small Molecules, School of Basic Medical Sciences, and Jinshan Hospital, Fudan University, Shanghai, China.
J Cardiovasc Transl Res. 2024 Feb;17(1):153-166. doi: 10.1007/s12265-023-10434-1. Epub 2023 Sep 15.
Macrophage is the main effector cell during atherosclerosis. We applied single-cell RNA sequencing (scRNA) data to investigate the role of macrophage subsets in atherosclerosis. Monocyte and macrophage clusters were divided into 6 subclusters. Each subcluster's markers were calculated and validated by immunofluorescence. Elevated macrophage subclusters in the WD group were subject to enrichment pathway analysis and exhibited different phenotypes. Pseudotime analysis shows the subclusters originate from monocytes. We cultured bone marrow-derived macrophages with CSF-1 and ox-LDL to simulate an atherosclerotic-like environment and detected the transformation of subclusters. Macrophage-Vegfa and Macrophage-C1qb increased in the WD group. Macrophage-Vegfa acquires the characteristics of phagocytosis and immune response, while Macrophage-C1qb is not involved in lipid metabolism. The two subclusters are both enriched in cell movement and migration pathways. Experimental verification proved Monocyte-Ly6C evolved into Macrophage-Vegfa and Macrophage-C1qb during atherosclerosis progression.
巨噬细胞是动脉粥样硬化过程中的主要效应细胞。我们应用单细胞 RNA 测序(scRNA)数据来研究巨噬细胞亚群在动脉粥样硬化中的作用。单核细胞和巨噬细胞簇被分为 6 个亚簇。通过免疫荧光验证计算每个亚簇的标记物。WD 组中升高的巨噬细胞亚簇进行富集途径分析,并表现出不同的表型。拟时分析表明亚簇来源于单核细胞。我们用 CSF-1 和 ox-LDL 培养骨髓来源的巨噬细胞来模拟动脉粥样硬化样环境,并检测亚簇的转化。WD 组中巨噬细胞-Vegfa 和巨噬细胞-C1qb 增加。巨噬细胞-Vegfa 获得了吞噬和免疫反应的特征,而巨噬细胞-C1qb 不参与脂质代谢。这两个亚簇都富集在细胞运动和迁移途径中。实验验证证明单核细胞-Ly6C 在动脉粥样硬化进展过程中演变为巨噬细胞-Vegfa 和巨噬细胞-C1qb。