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Abstract Neuroblastoma, glioma, rhabdomyosarcoma, leiomyosarcoma, and teratoma cells were shown to express an antigenic determinant of human Thy-1 with monoclonal antibody 390 (ab 390). Specificity of ab 390 for a determinant on Thy-1 was shown in three ways. 1) The distribution of antigenic determinant 390 (ag 390) among normal cells and tissues was that of human Thy-1. Quantitative absorption of ab 390 with adult tissues demonstrated a large quantity of ag 390 associated with brain, at least 90-fold less associated with kidney, and 150 to 10,000-fold less associated with lung, thymus, liver, adrenal, colon, and muscle. Ab 390 reacted strongly with cultured fibroblasts and also with 12% of thymocytes; it did not react with blood monocytes, lymphocytes, erythrocytes, or with bone marrow cells. 2) A molecule was isolated from deoxycholate solubilized human brain membranes by ab 390 affinity chromatography with Mr = 24,000. 3) Human brain Thy-1 that was purified by lentil lectin affinity chromatography specifically inhibited binding of ab 390 to LA-N-1 human neuroblastoma cells. In studies of 29 cultured tumor cell lines, ab 390 reacted strongly with gliomas and moderately with neuroblastomas, a rhabdomyosarcoma, a leiomyosarcoma, and teratomas. Its reactivity with medulloblastoma, melanoma, and carcinoma cell lines was weak or insignificant. A molecule with Mr = 26,000, which is the m.w. of fibroblast associated Thy-1, was purified from membranes of a neuroblastoma and a glioma cell line. Quantitative absorption of ab 390 with 50 noncultured tumors demonstrated that neuroblastomas, gliomas, and soft tissue sarcomas can express more ag 390 than all adult tissues except brain. Significant heterogeneity in the quantity of ag 390 associated with individual tumors within these positive classes was observed. These data suggest a variety of human tumor cells express Thy-1 on their surfaces. This expression appears to be appropriate for neuroblastoma, glioma, rhabdomyosarcoma, and leiomyosarcoma cells because normal cells of these same lineages also can express Thy-1.
Seeger et al. (Mon,) studied this question.