Stromal expression of Jagged 1 promotes colony formation by fetal hematopoietic progenitor cells

Blood. 1998 Sep 1;92(5):1505-11.

Abstract

The Notch signaling system regulates proliferation and differentiation in many tissues. Notch is a transmembrane receptor activated by ligands expressed on adjacent cells. Hematopoietic stem cells and early progenitors express Notch, making the stromal cells which form cell-cell contacts with progenitor cells candidate ligand-presenting cells in the hematopoietic microenvironment. Therefore, we examined primary stromal cell cultures for expression of Notch ligands. Using reverse transcription-polymerase chain reaction, in situ hybridization, immunohistochemistry, and Western blotting, we demonstrate expression of Jagged 1 in primary stromal cultures. To investigate if the stromal expression of Jagged 1 has functional effects on hematopoietic progenitors, we cultured CD34(+), c-kit+ hematopoietic progenitor cells derived from the aorto gonadal mesonephros region of day 11 mouse embryos on the Jagged 1(-) stromal cell line S17 and on S17 cells engineered to express Jagged 1. The presence of Jagged 1 increased the number of colonies formed in subsequent methylcellulose culture fourfold. Larger increases in colony numbers were observed under the same culture conditions with CD34(+), c-kit+ hematopoietic progenitor cells derived from d11 fetal liver. These results obtained in vitro table Jagged 1 as a candidate regulator of stem cell fate in the context of stromal microenvironments in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD34 / analysis
  • Aorta / cytology
  • Aorta / embryology
  • Blotting, Western
  • Calcium-Binding Proteins
  • Cells, Cultured
  • Embryo, Mammalian
  • Gene Expression*
  • Gonads / cytology
  • Gonads / embryology
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / immunology
  • Immunohistochemistry
  • In Situ Hybridization
  • Intercellular Signaling Peptides and Proteins
  • Jagged-1 Protein
  • Membrane Proteins / genetics*
  • Mesonephros / cytology
  • Mesonephros / embryology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins c-kit / analysis
  • RNA-Directed DNA Polymerase
  • Serrate-Jagged Proteins
  • Stromal Cells / metabolism*

Substances

  • Antigens, CD34
  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • Jag1 protein, mouse
  • Jagged-1 Protein
  • Membrane Proteins
  • Serrate-Jagged Proteins
  • Proto-Oncogene Proteins c-kit
  • RNA-Directed DNA Polymerase