| Literature DB >> 32579887 |
Immanuel Kwok1, Etienne Becht2, Yu Xia3, Melissa Ng2, Ye Chean Teh4, Leonard Tan5, Maximilien Evrard2, Jackson L Y Li2, Hoa T N Tran2, Yingrou Tan6, Dehua Liu2, Archita Mishra2, Ka Hang Liong2, Keith Leong2, Yuning Zhang2, Andre Olsson7, Chinmay Kumar Mantri8, Pavithra Shyamsunder9, Zhaoyuan Liu10, Cecile Piot2, Charles-Antoine Dutertre2, Hui Cheng11, Sudipto Bari12, Nicholas Ang2, Subhra K Biswas2, H Philip Koeffler13, Hong Liang Tey14, Anis Larbi2, I-Hsin Su15, Bernett Lee2, Ashley St John16, Jerry K Y Chan17, William Y K Hwang18, Jinmiao Chen2, Nathan Salomonis19, Shu Zhen Chong2, H Leighton Grimes20, Bing Liu21, Andrés Hidalgo22, Evan W Newell2, Tao Cheng11, Florent Ginhoux23, Lai Guan Ng24.
Abstract
Granulocyte-monocyte progenitors (GMPs) have been previously defined for their potential to generate various myeloid progenies such as neutrophils and monocytes. Although studies have proposed lineage heterogeneity within GMPs, it is unclear if committed progenitors already exist among these progenitors and how they may behave differently during inflammation. By combining single-cell transcriptomic and proteomic analyses, we identified the early committed progenitor within the GMPs responsible for the strict production of neutrophils, which we designate as proNeu1. Our dissection of the GMP hierarchy led us to further identify a previously unknown intermediate proNeu2 population. Similar populations could be detected in human samples. proNeu1s, but not proNeu2s, selectively expanded during the early phase of sepsis at the expense of monocytes. Collectively, our findings help shape the neutrophil maturation trajectory roadmap and challenge the current definition of GMPs.Entities:
Keywords: emergency granulopoiesis; granulocyte-monocyte progenitor; granulopoiesis; hematopoiesis; myeloid cells; myelopoiesis; neutrophil development; pro-neutrophil
Mesh:
Year: 2020 PMID: 32579887 DOI: 10.1016/j.immuni.2020.06.005
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745