A monoclonal antibody to murine CD45R distinguishes CD4 T cell populations that produce different cytokines

K Bottomly, M Luqman, L Greenbaum… - European journal of …, 1989 - Wiley Online Library
K Bottomly, M Luqman, L Greenbaum, S Carding, J West, T Pasqualini, DB Murphy
European journal of immunology, 1989Wiley Online Library
CD4 T cell clones have been shown to be functionally heterogeneous in the mouse.
However, it is not known if normal CD4 T cells are also functionally heterogeneous, or
whether functional specialization is a result of cloning and long‐term culture. To approach
this question, a monoclonal antibody reacting with a subset of CD4 T cells has been
prepared by immunization of rats with different cloned T cell lines all sharing the same
functional activity. This monoclonal antibody reacts with a subset of CD45 (T200) molecules …
Abstract
CD4 T cell clones have been shown to be functionally heterogeneous in the mouse. However, it is not known if normal CD4 T cells are also functionally heterogeneous, or whether functional specialization is a result of cloning and long‐term culture. To approach this question, a monoclonal antibody reacting with a subset of CD4 T cells has been prepared by immunization of rats with different cloned T cell lines all sharing the same functional activity. This monoclonal antibody reacts with a subset of CD45 (T200) molecules by binding to a determinant requiring the expression of the second variable exon of the CD45 molecule. Some CD4 T cells bear high levels of this marker, while others react only weakly. This antibody was used to separate CD4 T cells into two subpopulations. The brightly staining population was found to produce interleukin (IL) 2 and not IL 4, while the weakly staining population produced IL 4 and not IL 2. These data demonstrate that CD 4 T cells in normal mice are already functionally committed, and that they differentially express forms of CD45 that contain the second variable exon.
Wiley Online Library