祖细胞
生物
转录组
骨髓
干扰素
免疫学
细胞生物学
祖细胞
体外
细胞分化
分子生物学
干细胞
基因
基因表达
遗传学
作者
Federica Calzetti,Giulia Finotti,Nicola Tamassia,Francisco M. Bianchetto-Aguilera,Monica Castellucci,Stefania Canè,Silvia Lonardi,Chiara Cavallini,Alessandro Mattè,Sara Gasperini,Ilaria Signoretto,Fabio Benedetti,Massimiliano Bonifacio,William Vermi,Stefano Ugel,Vincenzo Bronte,Cristina Tecchio,Patrizia Scapini,Marco A. Cassatella
标识
DOI:10.1038/s41590-022-01189-z
摘要
Here we report the identification of human CD66b-CD64dimCD115- neutrophil-committed progenitor cells (NCPs) within the SSCloCD45dimCD34+ and CD34dim/- subsets in the bone marrow. NCPs were either CD45RA+ or CD45RA-, and in vitro experiments showed that CD45RA acquisition was not mandatory for their maturation process. NCPs exclusively generated human CD66b+ neutrophils in both in vitro differentiation and in vivo adoptive transfer experiments. Single-cell RNA-sequencing analysis indicated NCPs fell into four clusters, characterized by different maturation stages and distributed along two differentiation routes. One of the clusters was characterized by an interferon-stimulated gene signature, consistent with the reported expansion of peripheral mature neutrophil subsets that express interferon-stimulated genes in diseased individuals. Finally, comparison of transcriptomic and phenotypic profiles indicated NCPs represented earlier neutrophil precursors than the previously described early neutrophil progenitors (eNePs), proNeus and COVID-19 proNeus. Altogether, our data shed light on the very early phases of neutrophil ontogeny.
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