chitecture of the neutrophil compartment.
Cerezo-Wallis D., Rubio-Ponce A., Richter M., Pitino E., Kwok I., Marteletto G., Guanolema-Coba AC., Shih C., Huang R-K., Moraga A., Bravo NB., Doré S., Callejas S., Aragonés DG., Jiménez-Carretero D., Martin D., Ovadia S., Vicanolo T., Crainiciuc G., Sicilia J., Deng T., Martin A., Zhang J., Cuartero MI., Giraldo DM., Garcia-Culebras A., Aroca-Crevillen A., Martín-Salamanca S., Torroja C., Ruiz M., Ruano I., Ng MSF., Hou J., Wang Y., Zhang M., Pu J., Herruzo A., van Oordt DC., Chang S., Downie AE., Chen F., Graham AL., Gause WC., Fiset PO., Spicer JD., Heyn H., Zuriaga MA., Bernal JA., Udalova IA., Moro MA., de Bock K., Dopazo A., Fuster JJ., Sánchez-Cabo F., Nieto JC., Calvo GF., Skokowa J., Soehnlein O., Quail DF., Walsh LA., Ng LG., Hidalgo A., Ballesteros I.
Neutrophils exhibit remarkable phenotypic and functional diversity across tissues and diseases1,2, yet the lack of understanding of how this immune compartment is globally organized challenges translation to the clinic. Here we performed single-cell transcriptional profiling of neutrophils spanning 47 anatomical, physiological and pathological scenarios to generate an integrated map of the global neutrophil compartment in mice, which we refer to as NeuMap. NeuMap integrates and expands existing models3,4 to generate fundamental new insights; it reveals that neutrophils organize in a finite number of functional hubs that distribute sequentially during maturation to then branch out into interferon-responsive and immunosuppressive states, as well as a functionally silent state that dominates in the healthy circulation. Computational modelling and timestamp analyses identify prototypical trajectories that connect these hubs, and reveal that the dynamics and preferred paths vary during health, inflammation and cancer. We show that TGFβ, IFNβ and GM-CSF push neutrophils along the different trajectories, and projection of chromatin accessibility sites onto NeuMap reveals that the transcription factor JUNB controls angiogenic and immunosuppressive states and promotes tissue revascularization. The architecture of NeuMap appears to be conserved across sex, environmental and genetic backgrounds, as well as in humans. Finally, we show that NeuMap enables inference of the pathophysiological state of the host by profiling blood neutrophils. Our study delineates the global architecture of the neutrophil compartment and establishes a framework for exploration and exploitation of neutrophil biology.