Volume 19, Issue 10 pp. 1973-1976
Short Paper
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Transcription of unrearranged t cell receptor ∂ genes in cd3- major histocompatibility complex-unrestricted cytotoxic cells

Roberto Biassoni

Roberto Biassoni

Laboratory of Immunogenetics, National Institute of Allergy Infectious Diseases, National Institutes of Health, Bethesda

On leave from the Istituto Nazionale per la Ricerca sul Cancro.

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Silvano Ferrini

Silvano Ferrini

Istituto Nazinale per la Ricerca sul Cancro, Genoa

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Rafick P. Sekaly

Rafick P. Sekaly

Laboratory of Immunogenetics, National Institute of Allergy Infectious Diseases, National Institutes of Health, Bethesda

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Eric O. Long

Corresponding Author

Eric O. Long

Laboratory of Immunogenetics, National Institute of Allergy Infectious Diseases, National Institutes of Health, Bethesda

LIG-NIAID-NIH, Building 4, Room 213, Bethesda, MD 20892, USASearch for more papers by this author
First published: October 1989
Citations: 9

Abstract

Transcription of the T cell receptor (TcR) δ gene was detected in clones and in enriched populations of CD3- major histocompatibility complex-unrestricted cytotoxic cells. The transcripts were derived, at least in part, from unrearranged TcR δ genes, as shown by hybridization to a synthetic oligonucleotide probe corresponding to germ-line sequences just upstream of Jδ1. Transcripts from unrearranged TcR δ genes are similar in size to those from productively rearranged genes. The fact that the bulk of δ transcripts was derived from unrearranged genes was supported by the observation that TcR δ gene rearrangements were not detected in DNA isolated from an enriched CD3- cytotoxic cell population. Transcription of the TcR δ gene in CD3- cytotoxic cells is consistent with the notion that these cells belong to a T cell lineage.

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