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PMID: 2109035 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transgenic mice demonstrate that epithelial homing of gamma/delta T cells is determined by cell lineages independent of T cell receptor specificity.

The Journal of experimental medicine ·Vol. 171 ·No. 4 ·1990-04-01 ·Pages 1015-26

Bonneville M, Itohara S, Krecko EG, Mombaerts P, Ishida I, Katsuki M, Berns A, Farr AG, Janeway CA, Tonegawa S

Abstract

gamma/delta T cells with different TCR repertoires are compartmentalized in different epithelia. This raises the possibility that the TCR-gamma/delta directs homing of T cells to these epithelia. Alternatively, the signals that induce TCR-gamma/delta expression in developing T cells may also induce homing properties in such cells, presumably in the form of cell surface receptors. We have examined this issue by studying the homing of gamma/delta T cells in transgenic mice constructed with specific pairs of rearranged gamma and delta genes. In such mice, most gamma/delta T cells express the transgene-encoded TCR. We find that homing to both skin and gut epithelia is a property of T cells and is not determined by the type of gamma and delta genes used to encode their TCR. We also studied the effect of TCR replacement on the expression of Thy-1 and CD8 proteins on the gamma/delta T cells associated with gut epithelia. Our results show that the expression of the appropriate type of TCR-gamma/delta is not required for the Thy-1 expression by these T cells, suggesting that Thy-1 is not an activation marker. In contrast, CD8 expression by gut gamma/delta T cells seems to depend on the expression of the appropriate type of TCR.

MeSH Terms
Animals Antibodies, Monoclonal Antigens, Differentiation, T-Lymphocyte/analysis CD4 Antigens/analysis CD8 Antigens Epithelium/immunology Flow Cytometry Fluorescent Antibody Technique Mice Mice, Inbred C57BL Mice, Transgenic Receptors, Antigen, T-Cell/analysis,genetics T-Lymphocytes/immunology
Chemicals
Antibodies, Monoclonal Antigens, Differentiation, T-Lymphocyte CD4 Antigens CD8 Antigens Receptors, Antigen, T-Cell
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Bonneville M
Howard Hughes Medical Institute, Center for Cancer Research, Cambridge, Massachusetts.
Itohara S
Krecko E G
Mombaerts P
Ishida I
Katsuki M
Berns A
Farr A G
Janeway C A
Tonegawa S
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1990-04-01
Pages
1015-26
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2187834
Subset
IM
Grants
NIAID NIH HHS · AI17879 · United States
NIAID NIH HHS · AI24137 · United States
NCI NIH HHS · CA-28900 · United States
Analysis Services
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