Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice

J Exp Med. 1994 Nov 1;180(5):1955-60. doi: 10.1084/jem.180.5.1955.

Abstract

Interleukin 7 (IL-7) stimulates the proliferation of B cell progenitors, thymocytes, and mature T cells through an interaction with a high affinity receptor (IL-7R) belonging to the hematopoietin receptor superfamily. We have further addressed the role of IL-7 and its receptor during B and T cell development by generating mice genetically deficient in IL-7R. Mutant mice display a profound reduction in thymic and peripheral lymphoid cellularity. Analyses of lymphoid progenitor populations in IL-7R-deficient mice define precisely those developmental stages affected by the mutation and reveal a critical role for IL-7R during early lymphoid development. Significantly, these studies indicate that the phase of thymocyte expansion occurring before the onset of T cell receptor gene rearrangement is critically dependent upon, and mediated by the high affinity receptor for IL-7.

MeSH terms

  • Animals
  • Antigens, CD*
  • CD4 Antigens / analysis
  • CD8 Antigens / analysis
  • Female
  • Interleukin-7 / physiology*
  • Leukosialin
  • Lymphocytes / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Interleukin / deficiency
  • Receptors, Interleukin / physiology*
  • Receptors, Interleukin-2 / physiology
  • Receptors, Interleukin-7
  • Sialoglycoproteins / analysis

Substances

  • Antigens, CD
  • CD4 Antigens
  • CD8 Antigens
  • Interleukin-7
  • Leukosialin
  • Receptors, Interleukin
  • Receptors, Interleukin-2
  • Receptors, Interleukin-7
  • Sialoglycoproteins
  • Spn protein, mouse