Kubota K, Mizoguchi H, Miura Y, Kano S, Takaku F
Exp Hematol. 1978 Nov;6(10):791-800.
In order to study the pathogenesis of aplastic anemia in man, hemopoietic stem cells were investigated in 'aplastic mice' the aplasia being induced by the immunological method. C3H/He (H-2k, Mlsc) received 600 rad whole body x-irradiation followed by the transplantation of 10(7) lymph node cells prepared from B10.BR mic e (H-2k, Mlsb). The C3H/He mice developed pancytopenia and marrow hypoplasia 21 days after these treatments. The total number of nucleated cells, CFU-S and CFU-C in the marrow and the wet weight and CFU-C of the spleen were markedly reduced. These findings are consistent with those of aplastic anemia in man and the model may provide a useful tool for the investigation of the pathogenesis of this anemia. Control mice that received irradiation only recovered from the damage 21 days later, while control mice that receive lymph node cells only showed no hematological changes.
为了研究人类再生障碍性贫血的发病机制,对“再生障碍性小鼠”的造血干细胞进行了研究,其再生障碍是通过免疫方法诱导的。C3H/He(H-2k,Mlsc)小鼠接受600拉德全身X射线照射,随后移植从B10.BR小鼠(H-2k,Mlsb)制备的10(7)个淋巴结细胞。在这些处理后21天,C3H/He小鼠出现全血细胞减少和骨髓发育不全。骨髓中有核细胞、CFU-S和CFU-C的总数以及脾脏的湿重和CFU-C均明显减少。这些发现与人再生障碍性贫血的发现一致,该模型可能为研究这种贫血的发病机制提供一个有用的工具。仅接受照射的对照小鼠在21天后从损伤中恢复,而仅接受淋巴结细胞的对照小鼠未出现血液学变化。