Premium
Age‐related expression of TL antigen in AKR/J mice
Author(s) -
Peled Alpha,
HaranGhera Nechama
Publication year - 1984
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910340121
Subject(s) - spleen , bone marrow , antigen , leukemia , population , biology , antiserum , phenotype , immunology , microbiology and biotechnology , medicine , pathology , genetics , gene , environmental health
A survey of age‐related expression of thymus‐leukemia (TL) alloantigens (TL 1,2,4) among bone marrow, spleen and thymus cells of grossly normal and leukemic AKR/J mice is presented. The response of the stained cells to antisera directed against TL antigens was analysed by means of the fluorescence‐activated cell sorter (FACS) apparatus. A transient expression of TL antigens on cells among the bone marrow population was obsered in I‐ to 20‐day‐old AKR/J mice, followed by an undetectable level up to 3 months and its reappearance thereafter. Thymocytes expressed TL from the age of 4 months onwards, reaching a transient maximal level at the age of 6 months in females and 8 months in males. Subsequently, an agerelated decrease took place. In spleen cells from newborn mice TL expression was seen, followed by a rapid decrease to undetectable levels up to the age of 5‐6 months. In most tests the expression of TL.4 preceded the TL 1,2 phenotype. The frequency of TL+ leukemias was about 50% among the early‐occurring spontaneous leukemias (in 5‐ to 7‐month‐old mice) and decreased to 20% with age increase. Leukemia development following treatment with methyl‐nitrosourea (MNUA) or exposure to X‐rays increased the frequency of TL+ tumors to 75‐100%. These results suggest that heterogeneous target cells are involved in AKR leukemogenesis.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom