A checkpoint in B-lymphopoiesis related to Notch resistance

Biochem Biophys Res Commun. 2012 Jan 6;417(1):141-6. doi: 10.1016/j.bbrc.2011.11.072. Epub 2011 Nov 23.

Abstract

While murine B- and T-lymphopoiesis require overlapping molecules, they occur in separate organs: the bone marrow (BM) and the thymus, respectively. The BM microenvironment is incapable of supporting T-lymphopoiesis because of insufficient interactions of Notch1 with delta-like ligand (Dll). Notch1/Dll interactions also play a role in the suppression of B-lymphopoiesis in the thymus. However, it is still unclear whether the Notch1/Dll interaction alone explains why the thymus does not support B-lymphopoiesis. In this study, we compared the precursor population colonizing the thymus with that in the BM by culturing them on stromal cells expressing abundant Dll1. We demonstrated that Flt3(+) Il7r(+) B220(+) Cd19(+) BM cells gave rise to B cells under this condition. We defined them as resistant to Dll1. In the thymus, Dll1-resistant cells were undetectable. This suggested that the absence of Dll1-resistant cells might explain the absence of B-lymphopoiesis in the thymus.

MeSH terms

  • Animals
  • Antigens, CD19 / metabolism
  • B-Lymphocytes / immunology*
  • Cells, Cultured
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Leukocyte Common Antigens / metabolism
  • Lymphopoiesis*
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Receptor, Notch1 / metabolism*
  • Receptors, Interleukin-7 / metabolism
  • Thymus Gland / immunology*
  • fms-Like Tyrosine Kinase 3 / metabolism

Substances

  • Antigens, CD19
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Notch1 protein, mouse
  • Receptor, Notch1
  • Receptors, Interleukin-7
  • delta protein
  • Flt3 protein, mouse
  • fms-Like Tyrosine Kinase 3
  • Leukocyte Common Antigens