Fig. 1: scRNA-seq of pulmonary melanoma identifies gene signatures in CD206hi IMs, CD206lo IMs and recMacs.
From: Chemokine-defined macrophage niches establish spatial organization of tumor immunity

a, Unbiased UMAP clustering of scRNA-seq data from flow-sorted extravascular CD64⁺CD11b⁺ mononuclear phagocytes isolated from the lungs of C57BL/6 WT mice on day 16 after intravenous injection of 4 × 105 B16F10 melanoma cells. Clusters include AMs, IMs, recruited macrophages (recMacs), dendritic cells 1 (DC1), dendritic cells 2 (DC2), inflammatory DCs (Inf DC2), migratory DCs (Mig DCs), pre-DCs, plasmacytoid DCs (pDCs), neutrophils, eosinophils, basophils, mast cells, CD8⁺ T cells, CD4⁺ T cells, regulatory T (Treg) cells, double-negative T (DN T) cells, γδ T cells, natural killer (NK) cells, NK progenitors, B cells, innate lymphoid cells (ILC2), melanoma cells and cycling cells. b, Key signature genes defining the unbiased clusters as in a. c, UMAP of Pf4+C5ar1+Mafb+ IMs and Ly6c2+Fn1+Vcan+ recMacs as in a. d, Feature plots showing the expression of C1qb and Pf4 in IMs (left), expression of Folr2, Cd163, Mmp9 and Lyve1 in CD206hi IMs (middle) and expression of Ccr2, Mmp12, Mmp13 and Tmem119 in CD206lo IMs (right). e, Feature plots showing expression for Fn1, Ly6c2, Vcan and Thbs1 in recMacs. f, Feature plots showing the expression of Cxcl13, Cxcl9 and Cxcl10 in CD206hi IMs (left) and Spp1, Vegfa, Arg1 and Cd274 in recMacs and Trem2 in recMacs and IMs (right).