Volume 17, Issue 9 pp. 1387-1390
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Subpopulations of CD4, CD8 thymocytes

William C. Gause

Corresponding Author

William C. Gause

Cellular Immunology Section, Arthritis and Rheumatism Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda

National Institutes of Health, Building 10, Room 9N-218, Bethesda, MD 20892, USASearch for more papers by this author
John D. Mountz

John D. Mountz

Cellular Immunology Section, Arthritis and Rheumatism Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda

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Alfred D. Steinberg

Alfred D. Steinberg

Cellular Immunology Section, Arthritis and Rheumatism Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda

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First published: 1987
Citations: 7

Abstract

A population of highly purified CD4, CD8 thymocytes was analyzed by both flow microfluorometry and in situ hybridization in an attempt to further elucidate thymocyte subpopulations. The double-negative cells had a marked increase in expression of the c-myb and T cell gamma genes relative to unseparated thymocytes. Approximately 27% were Ly-24+, 8% Ly-6C+ and 6% 6B2+. All of the Ly-6C+ cells were also Ly-24+. A small population (6%) of the CD4, CD8 thymocytes had surface expression of the T cell receptor for antigen (F23.1); all were bright Ly-1+ and half were Ly-24+. These studies demonstrate that there are further subdivisions of the CD4, CD8 thymocytes based upon cell surface expression of markers previously found on bone marrow cells and their non-T cell progeny. Studies are in progress to determine whether these represent different stages of activation-maturation or different lineages of cells.

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