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突变小鼠L细胞:巨幼细胞贫血的一个模型。

Mutant mouse L-cells: a model for megaloblastic anaemia.

作者信息

Dardick I, Sheinin R, Setterfield G

出版信息

Br J Haematol. 1978 Aug;39(4):483-90. doi: 10.1111/j.1365-2141.1978.tb03617.x.

Abstract

When temperature-sensitive (ts) mutant lines of mouse L-cells, ts AIS9 and ts CI, are shifted from 34C to 38.5C, a rapid inhibition of DNA synthesis and mitosis occurs. During this phase, cell and nuclear growth continues and results in a substantial increase in cell and nuclear volume. Such cellular modifications are also associated with a marked dispersal of the condensed chromatin masses of interphase nuclei, so that after 48-72 h of incubation at 38.5C, nuclear profiles of both ts cell lines bear a striking resemblance to the nuclear features characteristic of megaloblastic anaemia. Despite these marked alterations in nuclear chromatin organization, morphometric analysis indicates that the volume of condensed chromatin does not decrease. Current biochemical, cytological and morphometric data on the two ts lines of mutant mouse L-cells during expression of the mutation, suggest that they might provide a useful model to further elucidate cytological features of megaloblastic anaemia.

摘要

当小鼠L细胞的温度敏感(ts)突变株ts AIS9和ts CI从34℃转移到38.5℃时,DNA合成和有丝分裂会迅速受到抑制。在此阶段,细胞和细胞核的生长仍在继续,导致细胞和细胞核体积大幅增加。这种细胞变化还与间期核中凝聚染色质团块的明显分散有关,因此在38.5℃孵育48 - 72小时后,两种ts细胞系的核形态与巨幼细胞贫血的核特征极为相似。尽管核染色质组织发生了这些显著变化,但形态计量分析表明凝聚染色质的体积并未减少。目前关于这两种ts突变小鼠L细胞系在突变表达过程中的生化、细胞学和形态计量学数据表明,它们可能为进一步阐明巨幼细胞贫血的细胞学特征提供一个有用的模型。

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