Functional differentiation of T cells in the intestine of T cell receptor transgenic mice

Stephen D. Hurst, Stephanie M. Sitterding, Sandy Ji, Terrence A. Barrett

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

The intestinal lamina propria (LP) is a major effector site of the mucosal immune system where antigen-specific and antigen-nonspecific factors shape the functional responses of CD4+ T helper cells. To study the functional differentiation of LP T helper cells we utilized DO11.10 T cell receptor (TCR) transgenic (Tg) mice that expressed a clonotypic TCR specific for a class II major histocompatibility complex-restricted peptide of chicken ovalbumin. The majority of cells expressing Tg TCR (Tg+) in peripheral lymphoid tissue expressed naive surface phenotypes whereas nearly all Tg+ T cells in the intestinal LP expressed an activated/memory-like phenotype. Flow cytometric analysis of Tg+ T cell populations revealed that a small proportion of cells in peripheral lymphoid tissue but nearly all cells in the LP expressed dual (Tg plus non-Tg) TCRs. In Tg x recombinase-activating- gene-1-deficient (Tg x RAG.1-(/)-) mice, splenic and LP T cells expressed naive surface phenotypes and produced cytokines equivalent to naive splenic cells from Tg x RAG.1+(/)+ mice. In contrast, Tg LP cells from Tg x RAG- 1+(/)+ mice produced 35-fold greater levels of interferon-γ and 5-fold greater levels of interleukin 4 compared with naive splenic cells. These findings suggested that activation of Tg+ T cells through endogenous non-Tg TCR had promoted the localization and differentiation of memory-like effector T helper cells in the intestine.

Original languageEnglish
Pages (from-to)3920-3925
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume94
Issue number8
DOIs
StatePublished - Apr 15 1997

ASJC Scopus subject areas

  • General

Fingerprint

Dive into the research topics of 'Functional differentiation of T cells in the intestine of T cell receptor transgenic mice'. Together they form a unique fingerprint.

Cite this