TY - JOUR
T1 - Failure of t cell receptor negative selection in murine intestinal intra-epitheliallymphocytes
AU - Murosaki, Shinji
AU - Yoshikai, Yasunobu
AU - Ishida, Atsunori
AU - Nakamura, Takao
AU - Matsuzaki, Goro
AU - Taki Moto, Hiroaki
AU - Yuuki, Hiroyuki
AU - Nomoto, Kikuo
N1 - Funding Information:
We thank Or R. T. Kubo, Dr J. A. Bluestone, Dr P. Marrack, Dr H. Hengartner and Dr K. Tomonari for providing mAb of H57-597, UC7-13D5and 145-2C11, KJ25, 44-22-11 and KT-11, and Dr T. Otani for providing SEA. This work was in part supported by grants to Y. Yoshikai from the Ministry of Education, Science and Culture, the Ministry of Health and Welfare, Special Coordination Funds of Science and Technology Agency of the Japanese Government and Fukuoka Cancer Association.
PY - 1991/10
Y1 - 1991/10
N2 - The intestinal intra-epithelial lymphocytes (IEL) are divided into several subsets on the basis of expression of T cell receptor (TCR) a/3 and y6, intensity of Thy-1 expression and expression ofLyt-3 chain. To investigate the differentiation pathway of the IEL, we examined the repertoire of\f0 segments of T cells in the IEL in BALB/c (H-2d, Mls-1b2a) or AKR/J (H-2k, Mls-1a2b) mice. Among freshly isolated IEL, an appreciable number of T cells bearing Vβ3 or Vβ11, which recognize Mls-2a- or MHC IE-encoded molecules respectively, were detected in BALB/c mice.Similarly, in AKR/J mice, IEL contained appreciable levels of V^6-bearing T cells. Vβ3- orVβ11 -bearing T cells in the IEL in BALB/c mice increased to a significant level when incubatedwith staphylococcal enterotoxin A which specifically stimulates V03- and Vg11 -bearing T cells.Most of IEL without clonal deletion expressed Lyt-2 but not Lyt-3 antigens. Such T ceils werehardly detected in other organs, including liver. Our results indicate that TCRa/3-bearing intestinalIEL that have not undergone negative selection may have differentiated outside the thymus, presumably at a local site of the intestine and can respond normally to the signal via their TCR.
AB - The intestinal intra-epithelial lymphocytes (IEL) are divided into several subsets on the basis of expression of T cell receptor (TCR) a/3 and y6, intensity of Thy-1 expression and expression ofLyt-3 chain. To investigate the differentiation pathway of the IEL, we examined the repertoire of\f0 segments of T cells in the IEL in BALB/c (H-2d, Mls-1b2a) or AKR/J (H-2k, Mls-1a2b) mice. Among freshly isolated IEL, an appreciable number of T cells bearing Vβ3 or Vβ11, which recognize Mls-2a- or MHC IE-encoded molecules respectively, were detected in BALB/c mice.Similarly, in AKR/J mice, IEL contained appreciable levels of V^6-bearing T cells. Vβ3- orVβ11 -bearing T cells in the IEL in BALB/c mice increased to a significant level when incubatedwith staphylococcal enterotoxin A which specifically stimulates V03- and Vg11 -bearing T cells.Most of IEL without clonal deletion expressed Lyt-2 but not Lyt-3 antigens. Such T ceils werehardly detected in other organs, including liver. Our results indicate that TCRa/3-bearing intestinalIEL that have not undergone negative selection may have differentiated outside the thymus, presumably at a local site of the intestine and can respond normally to the signal via their TCR.
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U2 - 10.1093/intimm/3.10.1005
DO - 10.1093/intimm/3.10.1005
M3 - Article
C2 - 1661605
AN - SCOPUS:0026044435
SN - 0953-8178
VL - 3
SP - 1005
EP - 1013
JO - International immunology
JF - International immunology
IS - 10
ER -