Cargando…
Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice
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 de...
Formato: | Texto |
---|---|
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1994
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191751/ https://www.ncbi.nlm.nih.gov/pubmed/7964471 |
_version_ | 1782147078357516288 |
---|---|
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2191751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21917512008-04-16 Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice J Exp Med Articles 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. The Rockefeller University Press 1994-11-01 /pmc/articles/PMC2191751/ /pubmed/7964471 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title | Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title_full | Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title_fullStr | Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title_full_unstemmed | Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title_short | Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
title_sort | early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191751/ https://www.ncbi.nlm.nih.gov/pubmed/7964471 |