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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Chronic lymphocytic leukemia lymphocytes lack the capacity to repair UVC-induced lesions.
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Chronic lymphocytic leukemia lymphocytes lack the capacity to repair UVC-induced lesions.

机译:慢性淋巴细胞性白血病淋巴细胞缺乏修复UVC诱导的病变的能力。

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摘要

Cells from chronic lymphocytic leukemia (CLL) patients and from healthy individuals were irradiated with UVC and incubated for varying periods of time. The number of single strand breaks and alkali-labile sites was determined by comet analysis. Unirradiated CLL and healthy cells exhibited no significant numbers of single strand breaks. The extent of DNA damage was found to increase with dose for both healthy and CLL cells. However, the CLL cells had much more extensive DNA fragmentation than healthy cells at each dose. Deoxyribonucleoside supplemented medium inhibited comet formation in both cell types. Thymidine alone produced the same effect. In healthy cells, repair of lesions was complete after 4 h of incubation as indicated by the absence of comet formation. The CLL cells exhibited no significant repair even after 48 h. CLL lymphocytes are killed by very low doses of UVC radiation. The results reported here suggest that this hypersensitivity results from the inability of CLL cells to repair UVC-induced DNA damage and a contributing factor is the low amounts of intracellular deoxyribonucleosides.
机译:用UVC照射来自慢性淋巴细胞性白血病(CLL)患者和健康个体的细胞,并孵育不同的时间。通过彗星分析确定单链断裂和碱不稳定位点的数量。未经辐照的CLL和健康细胞未表现出明显的单链断裂。对于健康细胞和CLL细胞,发现DNA损伤的程度随剂量增加而增加。但是,在每种剂量下,CLL细胞都比健康细胞具有更广泛的DNA片段化。补充脱氧核糖核苷的培养基在两种细胞类型中均抑制了彗星的形成。单独的胸腺嘧啶产生相同的效果。在健康细胞中,如无彗星形成所示,孵育4小时后即可完成病变修复。即使在48小时后,CLL细胞也没有表现出明显的修复。低剂量的UVC辐射可杀死CLL淋巴细胞。此处报道的结果表明,这种超敏反应是由于CLL细胞无法修复UVC诱导的DNA损伤而导致的,其诱因是细胞内脱氧核糖核苷的含量低。

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