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

Author:

Peschon J J1,Morrissey P J1,Grabstein K H1,Ramsdell F J1,Maraskovsky E1,Gliniak B C1,Park L S1,Ziegler S F1,Williams D E1,Ware C B1,Meyer J D1,Davison B L1

Affiliation:

1. Immunex Research and Development Corporation, Seattle, Washington 98101.

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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