Intermediate progenitor cells provide a transition between hematopoietic progenitors and their differentiated descendants

Development. 2021 Dec 15;148(24):dev200216. doi: 10.1242/dev.200216. Epub 2021 Dec 17.

Abstract

Genetic and genomic analysis in Drosophila suggests that hematopoietic progenitors likely transition into terminal fates via intermediate progenitors (IPs) with some characteristics of either, but perhaps maintaining IP-specific markers. In the past, IPs have not been directly visualized and investigated owing to lack of appropriate genetic tools. Here, we report a Split GAL4 construct, CHIZ-GAL4, that identifies IPs as cells physically juxtaposed between true progenitors and differentiating hemocytes. IPs are a distinct cell type with a unique cell-cycle profile and they remain multipotent for all blood cell fates. In addition, through their dynamic control of the Notch ligand Serrate, IPs specify the fate of direct neighbors. The Ras pathway controls the number of IP cells and promotes their transition into differentiating cells. This study suggests that it would be useful to characterize such intermediate populations of cells in mammalian hematopoietic systems.

Keywords: Drosophila; Blood cell development; Crystal cells; Hematopoiesis; Intermediate progenitor; Split GAL4.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blood Cells / cytology
  • Blood Cells / metabolism
  • Cell Differentiation / genetics
  • Cell Lineage / genetics
  • Drosophila Proteins / genetics*
  • Drosophila melanogaster / enzymology
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / growth & development
  • Hematopoiesis / genetics*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism
  • Hemocytes
  • Jagged-1 Protein / genetics*
  • Lectins / genetics
  • Receptors, Interleukin / genetics
  • Receptors, Notch / genetics*
  • Signal Transduction / genetics
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription Factors / genetics*

Substances

  • Drosophila Proteins
  • GAL4 protein, Drosophila
  • Hml protein, Drosophila
  • Jagged-1 Protein
  • Lectins
  • N protein, Drosophila
  • Receptors, Interleukin
  • Receptors, Notch
  • Ser protein, Drosophila
  • Transcription Factors
  • dome protein, Drosophila