It is known that rearrangement of the T cell antigen receptor (TCR) gene occurs in the thymus during T cell development and consequently results both in the deletion of DNA between the variable (V) and diversity/joining segments and in the formation of a circular DNA with recombination signal sequences. Here, we provide evidence that V alpha 14+ TCR gene rearrangements take place in extrathymic sites, such as bone marrow, liver, and intestine, but not in spleen, because we were able to detect frequent productive and nonproductive V alpha 14+ coding and signal sequences as a result of TCR rearrangements in extrathymic sites. Similar findings were also detected in athymic mice. Quantitative analysis shows that the relative amounts of V alpha 14 gene-mediated signal sequences in extrathymic tissues are higher than those in thymus. On the contrary, TCR rearrangements of V alpha 1.1 T cells, which are known to develop in the thymus, were mainly detected in the thymus, Peyer's patch, and spleen, but not in other extrathymic tissues, showing patterns distinct from V alpha 14 TCR rearrangements. These findings are evidence of extrathymic development of V alpha 14+ T cells. Differential characteristic TCR rearrangement patterns also indicate that distinct TCR repertoires are generated in different lymphoid tissues.
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1 May 1993
Article|
May 01 1993
Extrathymic development of V alpha 14-positive T cells.
Y Makino,
Y Makino
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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N Yamagata,
N Yamagata
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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T Sasho,
T Sasho
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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Y Adachi,
Y Adachi
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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R Kanno,
R Kanno
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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H Koseki,
H Koseki
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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M Kanno,
M Kanno
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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M Taniguchi
M Taniguchi
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
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Y Makino
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
N Yamagata
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
T Sasho
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
Y Adachi
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
R Kanno
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
H Koseki
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
M Kanno
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
M Taniguchi
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1993) 177 (5): 1399–1408.
Citation
Y Makino, N Yamagata, T Sasho, Y Adachi, R Kanno, H Koseki, M Kanno, M Taniguchi; Extrathymic development of V alpha 14-positive T cells.. J Exp Med 1 May 1993; 177 (5): 1399–1408. doi: https://doi.org/10.1084/jem.177.5.1399
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