| Literature DB >> 29466759 |
Maximilien Evrard1, Immanuel W H Kwok2, Shu Zhen Chong3, Karen W W Teng3, Etienne Becht3, Jinmiao Chen3, Je Lin Sieow3, Hweixian Leong Penny3, Goh Chi Ching3, Sapna Devi3, José Maria Adrover4, Jackson L Y Li5, Ka Hang Liong3, Leonard Tan3, Zhiyong Poon6, Shihui Foo3, Jia Wang Chua3, I-Hsin Su7, Karl Balabanian8, Françoise Bachelerie8, Subhra K Biswas3, Anis Larbi3, William Y K Hwang6, Vikas Madan9, H Phillip Koeffler10, Siew Cheng Wong3, Evan W Newell3, Andrés Hidalgo11, Florent Ginhoux3, Lai Guan Ng12.
Abstract
Neutrophils are specialized innate cells that require constant replenishment from proliferative bone marrow (BM) precursors as a result of their short half-life. Although it is established that neutrophils are derived from the granulocyte-macrophage progenitor (GMP), the differentiation pathways from GMP to functional mature neutrophils are poorly defined. Using mass cytometry (CyTOF) and cell-cycle-based analysis, we identified three neutrophil subsets within the BM: a committed proliferative neutrophil precursor (preNeu) which differentiates into non-proliferating immature neutrophils and mature neutrophils. Transcriptomic profiling and functional analysis revealed that preNeu require the C/EBPε transcription factor for their generation from the GMP, and their proliferative program is substituted by a gain of migratory and effector function as they mature. preNeus expand under microbial and tumoral stress, and immature neutrophils are recruited to the periphery of tumor-bearing mice. In summary, our study identifies specialized BM granulocytic populations that ensure supply under homeostasis and stress responses.Entities:
Keywords: Granulopoiesis; neutrophil development; neutrophil ontogeny; neutrophil precursors; trafficking
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Year: 2018 PMID: 29466759 DOI: 10.1016/j.immuni.2018.02.002
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745