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CD66b - CD64 dim CD115 - cells in the human bone marrow represent neutrophil-committed progenitors.

Federica CalzettiGiulia FinottiNicola TamassiaFrancisco Bianchetto-AguileraMonica CastellucciStefania CanèSilvia LonardiChiara CavalliniAlessandro MatteSara GasperiniIlaria SignorettoFabio BenedettiMassimiliano BonifacioWilliam VermiStefano UgelVincenzo BronteCristina TecchioPatrizia ScapiniMarco Antonio Cassatella
Published in: Nature immunology (2022)
Here we report the identification of human CD66b - CD64 dim CD115 - neutrophil-committed progenitor cells (NCPs) within the SSC lo CD45 dim CD34 + and CD34 dim/- 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.
Keyphrases
  • bone marrow
  • single cell
  • nk cells
  • endothelial cells
  • rheumatoid arthritis
  • mesenchymal stem cells
  • coronavirus disease
  • dendritic cells
  • stem cells
  • peripheral blood
  • induced apoptosis
  • systemic sclerosis
  • cell therapy