Expression of T-cell differentiation antigens on activated Thymocytes |
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Authors: | P Kisielow P Dráber |
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Affiliation: | 1. Ludwik Hirszfeld Institute of Immunology and Experimental Therapy of the Polish Academy of Sciences, Wroc?aw, Poland;2. Institute of Molecular Genetics of the Czechoslovak Academy of Sciences, Prague, Czechoslovakia |
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Abstract: | ![]() The expression of Thy 1, TL, Lyt1, and Lyt2 antigens on resting and proliferating thymocytes activated by concanavalin A in the presence of interleukin 2 has been studied by conventional complement-dependent cytotoxicity assay. The predominant population of resting thymocytes has a TL+Lytl+Lyt2+ phenotype while the predominant population of proliferating thymocytes has a TL — Lytl+Lyt2+ phenotype. Using several separation procedures such as agglutination by peanut lectin, BSA density gradient centrifugation, and pretreatment with high dilutions of anti-H-2 serum it was impossible to obtain a 100% pure population of TL+Lytl+Lyt2+ cells, suggesting that the population of resting immature thymocytes contains small subpopulations of phenotypically differentiated cells. The population of proliferating thymocytes is also phenotypically heterogenous and contains cells bearing all phenotypes that were described for different stages of T-cell differentiation, including TL+Lytl+Lyt2? and TL+Lytl?Lyt2+ with the following approximate frequency: TL+Lytl+Lyt2+—27%, TL+Lytl+Lyt2?—8%, TL+Lyt1?Lyt2+—4%, TL?Lytl+Lyt2+—45%, TL?Lyt1+Lyt2?—13%, TL?Lyt1?Lyt2+—3%. |
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