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N-甲基-N-亚硝基脲诱导的DNA链断裂和胸腺细胞死亡。

DNA strand breaks and death of thymocytes induced by N-methyl-N-nitrosourea.

作者信息

Ogiu T, Fukami H, Nishimura M

机构信息

Division of Physiology and Pathology, National Institute of Radiological Sciences, Chiba, Japan.

出版信息

J Cancer Res Clin Oncol. 1992;118(1):23-9. doi: 10.1007/BF01192307.

Abstract

N-Methyl-N-nitrosourea (MNU) is a potent carcinogen in various sites of experimental animals and induces thymic lymphoma in rats, which has long been hard to induce by any carcinogen. To analyze the action of MNU on thymocytes, DNA strand breaking in thymocytes from the MNU-treated rat and that in MNU-treated cultured thymocytes were assayed. Fluorometric analysis of DNA unwinding (FADU assay), first reported by Birnboim and Jevcak to detect X-ray-induced DNA damage, was modified and applied to detect DNA damage in thymocytes treated with MNU in vitro or in vivo. In the present modified method, cell lysate was admixed with 0.15 M sodium hydroxide, and DNA unwinding was processed at pH 12.0 for up to 2 h at 0 degree C in iced water. Double-stranded DNA remaining after alkaline reaction was detected by binding ethidium bromide and measuring its fluorescence. The severity of DNA damage, both in vivo and in vitro, depended on the MNU concentration. In addition, the sequential survival rate and cell-size distribution of thymocytes treated with MNU in vitro were investigated. A close relationship between the severity of DNA damage and cell death was demonstrated in MNU-treated thymocytes, and DNA damage by a non-cell-killing dose of MNU was detected with this FADU assay. MNU-induced cell death is not programmed as in apoptosis, which is caused in thymocytes physiologically, immunologically and by X-ray irradiation or corticoids.

摘要

N-甲基-N-亚硝基脲(MNU)是实验动物多个部位的强效致癌物,可诱发大鼠胸腺淋巴瘤,长期以来任何致癌物都难以诱发这种肿瘤。为分析MNU对胸腺细胞的作用,对经MNU处理的大鼠胸腺细胞以及经MNU处理的培养胸腺细胞中的DNA链断裂情况进行了检测。首次由Birnboim和Jevcak报道用于检测X射线诱导的DNA损伤的DNA解旋荧光分析(FADU分析)经过改进,用于检测体外或体内经MNU处理的胸腺细胞中的DNA损伤。在目前的改进方法中,将细胞裂解物与0.15 M氢氧化钠混合,并在0℃的冰水中于pH 12.0下处理DNA解旋长达2小时。通过结合溴化乙锭并测量其荧光来检测碱性反应后残留的双链DNA。体内和体外DNA损伤的严重程度取决于MNU的浓度。此外,还研究了体外经MNU处理的胸腺细胞的连续存活率和细胞大小分布。在经MNU处理的胸腺细胞中证明了DNA损伤的严重程度与细胞死亡之间存在密切关系,并且用这种FADU分析检测到了非细胞杀伤剂量的MNU引起的DNA损伤。MNU诱导的细胞死亡不像凋亡那样是程序性的,凋亡是胸腺细胞在生理、免疫、经X射线照射或使用皮质类固醇时所引发的。

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