祖细胞
祖细胞
生物
粒细胞
单核细胞
转录组
髓样
免疫学
人口
细胞生物学
计算生物学
遗传学
干细胞
基因
基因表达
医学
环境卫生
作者
Immanuel Kwok,Étienne Becht,Yu Xia,Melissa Ng,Ye Chean Teh,Leonard Tan,Maximilien Evrard,J Li,Hoa Thi Tran,Yingrou Tan,Dehua Liu,Archita Mishra,Ka Hang Liong,Keith Weng Kit Leong,Yuning Zhang,André Olsson,Chinmay Kumar Mantri,Pavithra Shyamsunder,Zhaoyuan Liu,Cécile Piot
出处
期刊:Immunity
[Elsevier]
日期:2020-06-23
卷期号:53 (2): 303-318.e5
被引量:215
标识
DOI:10.1016/j.immuni.2020.06.005
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI