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Radiation leukemia in C57BL/6 mice. III. Correlation of altered expression of terminal deoxynucleotidyl transferase to induction of leukemia

机译:C57BL / 6小鼠的放射性白血病。三,末端脱氧核苷酸转移酶表达改变与白血病诱导的相关性

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摘要

The expression of terminal deoxynucleotidyl transferase (TdT) in the thymus and bone marrow of irradiated mice has been examined. Mice given the leukemogenic regimen of irradiation of four weekly doses of 175 rads starting at 1 mo of age show a long-term elimination of TdT activity in the bone marrow and a reduction of TdT activity in thymocytes. In such mice, the reappearance of normal levels of TdT in the thymus appears to only be associated with the onset of overt leukemia. This effect on TdT expression was shown to be uniquely associated with the leukemogenic regimen of irradiation in that nonleukemogenic irradiation or variations such as bone marrow reconstitution or age which reduce leukemias did not show the same phenotypic effects on TdT expression. The basis for the loss of TdT- positive cells was shown not to be due to the lack of the requisite factors involved in differentiation, but rather to the ability of leukemogenic doses of irradiation to reduce or eliminate an inducible bone marrow stem cell. These results are discussed with respect to the possible mechanisms involved in radiation-induced leukemias in mice.
机译:检查了末端脱氧核苷酸转移酶(TdT)在辐照小鼠的胸腺和骨髓中的表达。从小鼠的成年年龄开始,给予每周四次剂量175 rads的辐射致白血病方案的小鼠显示出长期消除了骨髓中TdT活性并降低了胸腺细胞TdT活性。在此类小鼠中,胸腺中TdT正常水平的重新出现似乎仅与明显的白血病发作有关。该对TdT表达的作用显示出与辐射的致白血病方案独特地相关,因为非致白血病的辐射或降低白血病的诸如骨髓重构或年龄的变化对TdT表达没有表现出相同的表型作用。显示出TdT阳性细胞损失的基础不是由于缺乏参与分化的必要因素,而是由于产生白血病剂量的辐射能够减少或消除可诱导的骨髓干细胞。关于小鼠中辐射诱发的白血病所涉及的可能机制,讨论了这些结果。

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