CD66b-CD64dimCD115- cells in the human bone marrow represent neutrophil-committed progenitors

Nat Immunol. 2022 May;23(5):679-691. doi: 10.1038/s41590-022-01189-z. Epub 2022 Apr 28.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD*
  • Bone Marrow Cells
  • Bone Marrow*
  • COVID-19
  • Cell Adhesion Molecules*
  • Cell Differentiation*
  • GPI-Linked Proteins
  • Humans
  • Interferons
  • Neutrophils* / cytology
  • Receptor, Macrophage Colony-Stimulating Factor*
  • Receptors, IgG*

Substances

  • Antigens, CD
  • CEACAM8 protein, human
  • Cell Adhesion Molecules
  • GPI-Linked Proteins
  • Receptors, IgG
  • Interferons
  • Receptor, Macrophage Colony-Stimulating Factor