CYTOLYTIC ACTIVITY OF INTESTINAL INTRAEPITHELIAL LYMPHOCYTES IN GERM-FREE MICE IS STRAIN-DEPENDENT AND DETERMINED BY T-CELLS EXPRESSING GAMMA-DELTA-T-CELL ANTIGEN RECEPTORS

Citation
M. Kawaguchi et al., CYTOLYTIC ACTIVITY OF INTESTINAL INTRAEPITHELIAL LYMPHOCYTES IN GERM-FREE MICE IS STRAIN-DEPENDENT AND DETERMINED BY T-CELLS EXPRESSING GAMMA-DELTA-T-CELL ANTIGEN RECEPTORS, Proceedings of the National Academy of Sciences of the United Statesof America, 90(18), 1993, pp. 8591-8594
Citations number
25
Categorie Soggetti
Multidisciplinary Sciences
ISSN journal
00278424
Volume
90
Issue
18
Year of publication
1993
Pages
8591 - 8594
Database
ISI
SICI code
0027-8424(1993)90:18<8591:CAOIIL>2.0.ZU;2-G
Abstract
We have compared the cytolytic activities and the cellular composition s of the intestinal intraepithelial lymphocyte (i-IEL) populations in three different combinations of conventional (CV) and germ-free (GF) m ice. Cytolytic activity of i-IELs expressing gammabeta T-cell antigen receptors (TCRs) is strain dependent in CV mice (high vs. low), and th is strain-dependent variability is unaltered in the GF condition. Alth ough absolute numbers of gammadelta i-IELs are slightly decreased, the composition of CD8alphaalpha+ and CD4-CD8- subsets and the usage of T CR gamma- and delta-chain variable gene segments by gammadelta i-IELs remain the same in GF mice. By contrast, cytolytic activity of alphabe ta TCR-expressing i-IELs is uniformly high in CV mice but attenuated s harply in the GF condition. A conspicuous decrease in the total number s of alphabeta i-IELs is also noted, and CD8alphabeta+ and CD4+CD8+ su bsets are reduced, whereas the CD8alphaalpha+ subset is expanded in GF mice. These results indicate that microbial deprivation preferentiall y influences the alphabeta i-IEL population to decrease and become non cytolytic but has little effect on the pool size or characteristics of gammadelta i-IELs. Consequently, cytolytic activity of freshly isolat ed i-IELs from GF mice is determined by T cells expressing gammadelta TCRs and is found to be strain dependent.