Pathogenesis of a virus-induced leukemia in mice.
Pathogenesis of a virus-induced leukemia in mice.
复制标题
病毒诱导的小鼠白血病的发病机制。
DOI:
10.1093/jnci/26.1.189
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发表时间:
1961
期刊:
影响因子:
--
通讯作者:
B. Arnold
中科院分区:
文献类型:
--
作者:
T. Dunn;J. Moloney;A. W. Green;B. Arnold
Male BALB/c mice that received a cell-free extract from the spleens of mice with leukemia induced by a virus were compared with BALB/c mice of the same age and sex that received a cell-free extract from normal spleens. Untreated BALB/c mice were used as controls. Mice 6 weeks of age were chosen for the injections, since tissues from newborn mice are hard to handle, and a relatively low dose of virus was given to insure a gradual development of leukemia. No difference in the three groups could be detected until 8 weeks had elapsed, when many megakaryocytes containing granulocytes were observed in the bone marrow of the virus-injected mice. The next difference detected was a gradually increasing hyperplasia of the spleen in the virus-injected mice. A few mice showed a localized reticulum-cell hyperplasia in the lymph nodes. The most significant alterations appeared to be in the thymus, and, with one exception, it was in this organ that leukemia was first recognized in the treated mice. The thymus in one leukemic mouse did not contain malignant cells but showed a granulomatous reaction. A series of transplants made from the primary leukemias resulted in lymphocytic neoplasms with different biologic characteristics in regard to growth period, spread from the site of inoculation, and organ involvement. The transfer of tissue from hyperplastic spleens from mice with no morphologic evidence of leukemia reproduced the same sequence of preleukemic lesions that were observed after transfer of the cell-free extract. This study indicates that inoculation of the leukemia-inducing virus causes a derangement in certain reticular organs of mice which is conducive to the development of lymphocytic neoplasms. The virus described by Moloney may be acting like many other carcinogenic agents. Several incidental lesions appearing in experimental, control, and stock BALB/c mice are described.