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PMID: 8943725 Published · ppublish English Comparative Study Journal Article

Development and cytolytic function of intestinal intraepithelial T lymphocytes in antigen-minimized mice.

Immunology ·Vol. 89 ·No. 2 ·1996-10-00 ·Pages 268-73

Kawaguchi-Miyashita M, Shimizu K, Nanno M, Shimada S, Watanabe T, Koga Y, Matsuoka Y, Ishikawa H, Hashimoto K, Ohwaki M

Abstract

Intraepithelial T lymphocytes in the small intestine (IEL) consist of alpha beta T-cell receptor (TCR)-bearing T cells (alpha beta-IEL) and gamma delta TCR-bearing T cells (gamma delta-IEL). Development and cytolytic activation of alpha beta-IEL sharply attenuate in germ-free (GF) mice fed a natural diet (Nat-GF), but the number and cytotoxicity of gamma delta-IEL are comparable between conventional (CV) and Nat-GF mice. In this report, we compared the properties of IEL in Nat-GF mice and GF mice fed antigen-minimized diet (AgM-GF mice) of C57BL/6 strain to evaluate an influence of gut antigenic load on IEL development. Numbers of alpha beta-IEL and gamma delta-IEL in AgM-GF mice were less by 1.9- and 1.4-fold than those in Nat-GF mice, respectively. Significant decreases in the proportions of CD4+8-, CD4-8 alpha beta +, and CD4+8+ subsets and a resultant increase in the ratio of CD4-8 alpha alpha + subset were evident in alpha beta-IEL of Nat-GF mice compared with CV mice, but the subset constitution of alpha beta-IEL was similar between Nat-GF and AgM-GF mice. In contrast, relative composition of gamma delta-IEL was not different between CV, Nat-GF, and AgM-GF mice. alpha beta-IEL displayed low cytolytic activity in Nat-GF mice and were almost deprived of their cytotoxicity under the antigen-minimized condition. While gamma delta-IEL were strongly cytolytic in Nat-GF mice their cytolytic activity was remarkably reduced in AgM-GF mice. These results indicate that gamma delta-IEL are activated independently of microbial colonization in the gastrointestinal tract but their activation occurs in response to the exogenous antigenic substances other than live micro-organisms.

MeSH Terms
Animals Antigens/administration & dosage,immunology Cytotoxicity, Immunologic Diet Epithelium/immunology Female Germ-Free Life Intestinal Mucosa/immunology Intestine, Small/immunology Male Mice Mice, Inbred C57BL Receptors, Antigen, T-Cell/immunology Receptors, Antigen, T-Cell, alpha-beta/immunology Receptors, Antigen, T-Cell, gamma-delta/immunology T-Lymphocytes/immunology
Chemicals
Antigens Receptors, Antigen, T-Cell Receptors, Antigen, T-Cell, alpha-beta Receptors, Antigen, T-Cell, gamma-delta
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Kawaguchi-Miyashita M
Yakult Central Institute for Microbiological Research, Tokyo, Japan.
Shimizu K
Nanno M
Shimada S
Watanabe T
Koga Y
Matsuoka Y
Ishikawa H
Hashimoto K
Ohwaki M
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Article Info
Journal
Immunology
Abbr.
Immunology
ISSN
0019-2805
Published
1996-10-00
Pages
268-73
Language
English
Region
England
NLM ID
0374672
PMCID
PMC1456489
Subset
IM
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