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Fig. 4 | Genome Medicine

Fig. 4

From: Single-cell transcriptomics reveal distinct immune-infiltrating phenotypes and macrophage–tumor interaction axes among different lineages of pituitary neuroendocrine tumors

Fig. 4

Three distinct subtypes of tumor-associated macrophage in three different PitNETs lineages. A UMAP map depicting macrophage cells color-coded by subtypes. B Dot plot displaying the specific marker genes for the five subtypes of macrophages. C The percentage of the five subtypes of macrophages observed in the three lineages. P-values are calculated using ANOVA. D–E. Violin plots show marker genes (D) expression levels and cell abundance (E) for the five subtype macrophages of three lineages. P-values were calculated using the Wilcoxon rank-sum test. F–H. Immunofluorescence (IF) image demonstrating the cell distribution of CX3CR1+ (F), GPNMB+ (G), and C1Q+ (H) macrophages in the three lineage tumor cells. I. Flow cytometry data presents the proportion of CX3CR1+ macrophages in the population across the three lineages. P-values were calculated using the Wilcoxon rank-sum test. Results are presented as mean ± standard error of the mean in bar plots. J Trajectory plot of monocytes and the five subtypes of macrophages in a two-dimensional state-space inferred by Monocle 2 analysis (up) and the transition trajectories along pseudotime (down). K Three-phase distribution of C1Q+ macrophages and CX3CR1+ macrophages along pseudotime. Heatmap depicting the dynamic expression changes of genes and related pathways of C1Q+ macrophages and CX3CR1+ macrophages along pseudotime

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