Abstract
One of the TLMA (rat T-lymphocyte-macrophage-associated antigens) was characterized as asialo GM1, Gal(beta, 1-3)GalNAc(beta, 1-4)Gal(beta, 1-1)-Cer by two assay methods using monospecific anti-asialo GM1 antibody, immunocytotoxicity testing and immunostaining. Nylon column-enriched T lymphocytes (non-adherent cells) were highly cytolyzed by anti-asialo GM1 antiserum and complement as compared with adherent cells (non T cells). Forty % of peritoneal exudate macrophages and 20% of granulocytes were also cytolyzed by anti-asialo GM1 antiserum. On the other hand, 5% of thymic cells and 60-80% of lymph node T cells were immunostained by anti-asialo GM1 antibody. These asialo GM1-positive cells in thymus were found to be localized in the cortico-medulla junction. About 20% of macrophages and 2)% of granulocytes were also immunostained by anti-asialo GM1 F (ab')2 fragment. These results strongly support the previous conclusion that TLMA can be identified as asialo GM1. Asialo GM1 was universally expressed on a certain population of macrophages of various tissues, but not on all of the population. Alveolar macrophages were also asialo GM1-positive.
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