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在T和B细胞白血病中,2'-脱氧助间型霉素通过dATP介导对DNA连接酶的抑制作用。

dATP-mediated inhibition of DNA ligase by 2'-deoxycoformycin in T and B cell leukemia.

作者信息

Lamballe F, Le Prise P Y, Le Gall E, David J C

机构信息

Laboratoire de Biochimie du Développement, UA CNRS No. 256, Université de Rennes, France.

出版信息

Leukemia. 1989 Feb;3(2):97-103.

PMID:2783473
Abstract

2'-Deoxycoformycin (dCF), a potent adenosine deaminase inhibitor, has been reported to display greater toxicity for T than for B lymphoblasts. Since this compound can block DNA replication and since this effect is mediated by the intracellular ATP/dATP balance, its possible effect on DNA ligase was investigated. dCF at relatively low concentrations (1 microM), in association with dATP (100 microM), is a strong inhibitor of DNA ligase in T blasts, whereas it has no significant effect in B blasts at this concentration. The AMP-ligase complex is the target of the observed inhibition because the combined presence of the inhibitor and dATP results in a more stable dAMP-ligase complex. Because of this observation and of the greater adenosine deaminase activity observed in T cells, the dATP mediated dCF inhibition of ligase might be the crucial replication target of T cell toxicity. These observations are discussed in terms of T immunodeficiencies including Graft Versus Host Disease and related syndromes.

摘要

2'-脱氧助间型霉素(dCF)是一种有效的腺苷脱氨酶抑制剂,据报道,它对T淋巴母细胞的毒性比对B淋巴母细胞更大。由于该化合物可阻断DNA复制,且这种作用是由细胞内ATP/dATP平衡介导的,因此研究了其对DNA连接酶的可能影响。相对低浓度(1微摩尔)的dCF与dATP(100微摩尔)联合使用时,是T淋巴母细胞中DNA连接酶的强抑制剂,而在此浓度下对B淋巴母细胞无显著影响。AMP-连接酶复合物是观察到的抑制作用的靶点,因为抑制剂和dATP的共同存在会导致形成更稳定的dAMP-连接酶复合物。基于这一观察结果以及在T细胞中观察到的更高的腺苷脱氨酶活性,dATP介导的dCF对连接酶的抑制作用可能是T细胞毒性的关键复制靶点。将根据包括移植物抗宿主病和相关综合征在内的T细胞免疫缺陷来讨论这些观察结果。

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