Synthesis and release of thymidine by macrophages.

Synthesis and release of thymidine by macrophages.
复制标题

巨噬细胞合成和释放胸苷。

DOI:
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发表时间:
1977
影响因子:
4.4
通讯作者:
E. Unanue
E. Unanue
中科院分区:
医学2区
文献类型:
--
作者:
M. Stadecker;J. Calderón;M. Karnovsky;E. Unanue

文献摘要

被引文献

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对巨噬细胞上清中发现的DNA合成和细胞增殖抑制剂进行进一步分析。得出以下结论:a.从生物化学角度来看,从三种不同薄层体系的迁移和凝胶过滤来看,抑制剂似乎是胸苷。b.该抑制剂被证明是由巨噬细胞单层用放射性标记的胸苷前体(如14c -甲酸酯)脉冲重新合成的。c.组织培养液中存在的抑制剂的量被证明足以阻止EL-4白血病细胞系的生长,这种方式可以通过添加2'-脱氧胞苷来阻止。EL-4细胞系对胸苷阻断的敏感性明显高于许多不同的细胞。
An inhibitor of DNA synthesis and cell proliferation found in macrophage supernatants was subjected to further analysis. The following conclusions were drawn: a. Biochemically, the inhibitor appeared to be thymidine, judging from the migration in three different thin-layer systems and on gel filtration. b. The inhibitor was shown to be synthesized de novo by macrophage monolayers pulsed with a radiolabeled precursor of thymidine such as 14C-formate. c. The amount of inhibitor present in tissue culture fluids proved to be sufficient to block the growth of the EL-4 leukemia cell line in a manner that could be prevented with the addition of 2'-deoxycytidine. The EL-4 line was considerably more sensitive to thymidine blockade than a number of different cells tested.