生物
巨噬细胞
细胞
计算生物学
细胞生物学
免疫学
遗传学
体外
作者
Kevin Mulder,Amit A. Patel,Wan Ting Kong,Cécile Piot,Evelyn Halitzki,Garett Dunsmore,Shabnam Khalilnezhad,Sergio Erdal Irac,Agathe Dubuisson,Marion Chevrier,Xiao Meng Zhang,John Kit Chung Tam,Tony Kiat Hon Lim,Regina Men Men Wong,Rhea Pai,Ahmed Ibrahim Samir Khalil,Pierce K. H. Chow,Sunny Z. Wu,Ghamdan Al‐Eryani,Daniel Roden
出处
期刊:Immunity
[Cell Press]
日期:2021-07-30
卷期号:54 (8): 1883-1900.e5
被引量:409
标识
DOI:10.1016/j.immuni.2021.07.007
摘要
Mononuclear phagocytes (MNPs) encompass dendritic cells, monocytes, and macrophages (MoMac), which exhibit antimicrobial, homeostatic, and immunoregulatory functions. We integrated 178,651 MNPs from 13 tissues across 41 datasets to generate a MNP single-cell RNA compendium (MNP-VERSE), a publicly available tool to map MNPs and define conserved gene signatures of MNP populations. Next, we generated a MoMac-focused compendium that revealed an array of specialized cell subsets widely distributed across multiple tissues. Specific pathological forms were expanded in cancer and inflammation. All neoplastic tissues contained conserved tumor-associated macrophage populations. In particular, we focused on IL4I1+CD274(PD-L1)+IDO1+ macrophages, which accumulated in the tumor periphery in a T cell-dependent manner via interferon-γ (IFN-γ) and CD40/CD40L-induced maturation from IFN-primed monocytes. IL4I1_Macs exhibited immunosuppressive characteristics through tryptophan degradation and promoted the entry of regulatory T cell into tumors. This integrated analysis provides a robust online-available platform for uniform annotation and dissection of specific macrophage functions in healthy and pathological states.
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