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CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice

Rather unexpectedly, major histocompatibility complex class II- deficient mice have a significant population of peripheral CD4+ T lymphocytes. We have investigated these cells at the population and clonal levels. CD4+ T lymphocytes from class II-deficient animals are thymically derived, appear early...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192275/
https://www.ncbi.nlm.nih.gov/pubmed/7561702
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collection PubMed
description Rather unexpectedly, major histocompatibility complex class II- deficient mice have a significant population of peripheral CD4+ T lymphocytes. We have investigated these cells at the population and clonal levels. CD4+ T lymphocytes from class II-deficient animals are thymically derived, appear early in ontogeny, exhibit the phenotype of resting memory cells, are potentially functional by several criteria, and have a diverse T cell receptor repertoire. They do not include substantially elevated numbers of NK1.1+ cells. Hybridomas derived after polyclonal stimulation of the CD4+ lymphocytes from class II- deficient animals include a subset with an unusual reactivity pattern, responding to splenocytes from many mouse strains including the strain of origin. Most members of this subset recognize the major histocompatibility complex class Ib molecule CD1; their heterogeneous reactivities and T cell receptor usage further suggest the involvement of peptides and/or highly variable posttranslational modifications.
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spelling pubmed-21922752008-04-16 CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice J Exp Med Articles Rather unexpectedly, major histocompatibility complex class II- deficient mice have a significant population of peripheral CD4+ T lymphocytes. We have investigated these cells at the population and clonal levels. CD4+ T lymphocytes from class II-deficient animals are thymically derived, appear early in ontogeny, exhibit the phenotype of resting memory cells, are potentially functional by several criteria, and have a diverse T cell receptor repertoire. They do not include substantially elevated numbers of NK1.1+ cells. Hybridomas derived after polyclonal stimulation of the CD4+ lymphocytes from class II- deficient animals include a subset with an unusual reactivity pattern, responding to splenocytes from many mouse strains including the strain of origin. Most members of this subset recognize the major histocompatibility complex class Ib molecule CD1; their heterogeneous reactivities and T cell receptor usage further suggest the involvement of peptides and/or highly variable posttranslational modifications. The Rockefeller University Press 1995-10-01 /pmc/articles/PMC2192275/ /pubmed/7561702 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
CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title_full CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title_fullStr CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title_full_unstemmed CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title_short CD1-restricted CD4+ T cells in major histocompatibility complex class II-deficient mice
title_sort cd1-restricted cd4+ t cells in major histocompatibility complex class ii-deficient mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192275/
https://www.ncbi.nlm.nih.gov/pubmed/7561702