Natural killer activity in the rat. III. Characterization of transplantable large granular lymphocyte (LGL) leukemias in the F344 rat

• Published in: The Journal of immunology (1950) Vol. 132; no. 1; pp. 534 - 540
• Main Authors: Reynolds, CW, Bere, EW, Jr, Ward, JM
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Am Assoc Immnol 01.01.1984; American Association of Immunologists
• Subjects: Animals; Antibodies, Monoclonal - immunology; Antigens, Neoplasm - immunology; Antigens, Surface - immunology; Biological and medical sciences; Cell Line; Cell Transformation, Neoplastic - immunology; Cell Transformation, Neoplastic - pathology; Cytotoxicity, Immunologic; Epitopes; Killer Cells, Natural - immunology; Killer Cells, Natural - pathology; Leukemia, Experimental - immunology; Leukemia, Experimental - pathology; Medical sciences; Mice; Neoplasm Transplantation; Organ Specificity; Rats; Rats, Inbred F344; Rats, Inbred WF; Transplantability; Tumor cell; Tumors; Transplantability; Rat; Leukemia; Rodentia; Cytotoxicity; Malignant hemopathy; Immunological method; Natural killer cell; Vertebrata; Mammalia; Animal; Experimental tumor; Macrophage
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.132.1.534

Six transplantable large granular lymphocyte (LGL) tumor lines in F344 rats were examined for natural killer (NK) and antibody-dependent cell-mediated cytotoxicity. Tumor cells from all six lines were highly cytotoxic, even at low effector to target ratios, when tested against NK-susceptible targets, but were unreactive against an NK-resistant target (C58NT)D) and a macrophage-susceptible target (P815). Three lines showed significant levels of lysis against antibody-coated tumor cells. After in vivo transplantation, the levels of cytotoxicity steadily increased in three lines and decreased in one. The cytotoxic activity of one line (RNK-16) remained high through 12 transplant generations. Tumor cells injected i.p. spread via the lymphatics to regional lymph nodes, mediastinal nodes, blood, and eventually the bone marrow. Leukemia occurred concurrently with organ enlargement and increased levels of NK. Studies in (F344 X W/Fu)F1 rats clearly demonstrated that the cytotoxic cells from leukemic animals were the transplanted tumor cells themselves and not merely the activation of normal host LGL. These results demonstrate that naturally occurring, transplantable LGL leukemias are an easily obtainable and excellent source of materials for those studies requiring a large number of functionally active LGL.