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From the Division of Immunology, Department of Medicine, Stanford University School of Medicine, Stanford, California 94305
Abstract
In the present study, conditions are described for the selective detection of specific 125I-(T, G)-A--L binding to peripheral B and T cells. The following observations were made: 1) B cells appear to have at least 5 times more antigen receptors than do T cells. 2) When cells were allowed to react with antigen at 37°C instead of at 4°C, this had no influence on the frequency of B-ABC. In contrast, the number of T-ABC was increased 2- to 3-fold. This increase could be prevented by sodium azide, suggesting that the exposure of antigen-binding receptors on the surface of T cells depends on cellular metabolic activity. 3) Inhibition studies with chemical analogs of (T, G)-A--L revealed a different specificity of B and T cells. Whereas excess unlabeled (T, G)-A--L, (Phe, G)-A--L and (H, G)-A--L could each block 125I-(T, G)-A--L binding to B cells, only unlabeled (T, G)-A--L could inhibit specific T-ABC. Altogether, these observations provide further evidence for profound differences between B and T cell antigen receptors.
Footnotes
1 This research was supported by United States Public Health Service research Grant AI 07757.
2 Recipient of Dernham Fellowship, J-195, from the American Cancer Society, California Division.
3 Senior Investigator of the Arthritis Foundation.
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