| Literature DB >> 35484408 |
Federica Calzetti1, Giulia Finotti1, Nicola Tamassia1, Francisco Bianchetto-Aguilera1, Monica Castellucci2, Stefania Canè3, Silvia Lonardi4, Chiara Cavallini5, Alessandro Matte6, Sara Gasperini1, Ilaria Signoretto1, Fabio Benedetti7, Massimiliano Bonifacio7, William Vermi4, Stefano Ugel3, Vincenzo Bronte3, Cristina Tecchio7, Patrizia Scapini1, Marco A Cassatella8.
Abstract
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.Entities:
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Year: 2022 PMID: 35484408 DOI: 10.1038/s41590-022-01189-z
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 31.250