Volume 17, Issue 8 pp. 1209-1212
Short paper
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Cloned human CD3 lymphocytes with natural killerlike activity do not express nor rearrange T cell receptor gamma genes

Frédéric Triebel

Corresponding Author

Frédéric Triebel

Unité d'Immunology Cellulaire, Département de Biologie Clinique, Institut Gustave-Roussy, Villejuif

Unité d'Immunologie Cellulaire, Institut Gustave-Roussy, rue Camille Desmoulins, Villejuif, FranceSearch for more papers by this author
Marita Graziani

Marita Graziani

Unité d'Immunology Cellulaire, Département de Biologie Clinique, Institut Gustave-Roussy, Villejuif

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Florence Faure

Florence Faure

Unité d'Immunology Cellulaire, Département de Biologie Clinique, Institut Gustave-Roussy, Villejuif

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Setsuko Jitsukawa

Setsuko Jitsukawa

Unité d'Immunology Cellulaire, Département de Biologie Clinique, Institut Gustave-Roussy, Villejuif

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Thierry Hercend

Thierry Hercend

Unité d'Immunology Cellulaire, Département de Biologie Clinique, Institut Gustave-Roussy, Villejuif

Special fellow of the Leukemia Society of America.

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First published: 1987
Citations: 17

Abstract

Here we report the characterization of T cell receptor (TCR) gene activation in 14 CD3 cloned lymphocytes with natural killer-like activity from different origins. No transcription of either α or β or γ genes is detected in any of these clones. All Jβ, Cβ clusters are in germ-line configuration. The 5 presently described Jγ loci (JγP1, JγP, Jγ1, JγP2, Jγ2) are also in germ-line configuration on each chromosome. These results indicate that several distinct populations of CD3 cloned NK cells do not use γ gene products as a recognition structure. Perhaps more importantly, these cells do not appear to be engaged in the earliest presently known stage of T lymphocyte differentiation, namely rearrangement at one of the Jγ loci.

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