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低剂量(1-10 Gy)照射下染色质结构对CHO-K1和xrs1细胞初始DNA损伤及放射敏感性的影响

The influence of chromatin structure on initial DNA damage and radiosensitivity in CHO-K1 and xrs1 cells at low doses of irradiation 1-10 Gy.

作者信息

Roos W P, Binder A, Böhm L

机构信息

Department of Radiation Oncology, Faculty of Medical Sciences and Tygerberg Hospital, University of Stellenbosch, PO Box 19063, Tygerberg 7505, South Africa.

出版信息

Radiat Environ Biophys. 2002 Sep;41(3):199-206. doi: 10.1007/s00411-002-0166-3. Epub 2002 Sep 7.

Abstract

Mitotic compaction of chromatin was generated by treatment of cells with nocodazole. Alternatively, chromatin structure was altered by incubating cells in 500 mM NaCl. The irradiation response in the dose range of 1-10 Gy was measured by colony assay and by a modified fluorometric analysis of DNA unwinding (FADU) assay which measures the amount of undamaged DNA by EtBr fluorescence. Cell survival curves of irradiated CHO-K1 cells showed that treatment with nocodazole increases radiosensitivity as indicated by a decrease of the mean inactivation dose (D) from 4.446 to 4.376. Nocodazole treatment increased the initial radiation-induced DNA damage detected by the FADU assay from 7% to 13%. In repair-defective xrs1 cells, the same conditions increased the radiosensitivity from 1.209 to 0.7836 and the initial DNA damage from 43% to 57%. Alterations to chromatin structure by hypertonic medium increased radiosensitivity in CHO-K1 cells from of 4.446 to 3.092 and the initial DNA damage from 7% to 15%. In xrs1 cells these conditions caused radiosensitivity to decrease from 1.209 to 1.609 and the initial DNA damage to decrease from 43% to 36%. Disruption of chromatin structure by hypertonic treatment was found to be time-dependent. A threefold increase of exposure time to hypertonic medium from 40 to 120 min increased the initial DNA damage in CHO-K1 cells from 7% to 18% but decreased initial DNA damage in xrs1 cells from 43% to 21%. Perturbation of chromatin structure with hypertonic treatment has been shown to increase the radiosensitivity and the initial DNA damage in repair-competent CHO-K1 cells and decrease the radiosensitivity and DNA damage in repair-defective xrs1 cells. Hypertonic treatment thus abolishes differences in chromatin structure between cell lines and differences in initial DNA damage. Radiosensitivity and initial DNA damage are correlated ( r(2)=0.92; p=0.0026) and this correlation also holds when chromatin compaction is altered. The experiments demonstrate that initial DNA damage and chromatin structure are major determinants of radiosensitivity.

摘要

用诺考达唑处理细胞可诱导染色质的有丝分裂浓缩。另外,通过将细胞置于500 mM NaCl中孵育来改变染色质结构。通过集落测定法和改良的DNA解旋荧光分析(FADU)测定法来测量1-10 Gy剂量范围内的辐射反应,FADU测定法通过溴化乙锭荧光来测量未受损DNA的量。照射后的CHO-K1细胞的存活曲线表明,诺考达唑处理增加了放射敏感性,平均失活剂量(D)从4.446降至4.376。诺考达唑处理使FADU测定法检测到的初始辐射诱导的DNA损伤从7%增加到13%。在修复缺陷的xrs1细胞中,相同条件下放射敏感性从1.209增加到0.7836,初始DNA损伤从43%增加到57%。高渗培养基改变染色质结构使CHO-K1细胞的放射敏感性从4.446增加到3.092,初始DNA损伤从7%增加到15%。在xrs1细胞中,这些条件导致放射敏感性从1.209降至1.609,初始DNA损伤从43%降至36%。发现高渗处理破坏染色质结构具有时间依赖性。将高渗培养基的暴露时间从40分钟增加到120分钟,使CHO-K1细胞的初始DNA损伤从7%增加到18%,但使xrs1细胞的初始DNA损伤从43%降至21%。已表明高渗处理扰乱染色质结构会增加有修复能力的CHO-K1细胞的放射敏感性和初始DNA损伤,并降低修复缺陷的xrs1细胞的放射敏感性和DNA损伤。因此,高渗处理消除了细胞系之间染色质结构的差异以及初始DNA损伤的差异。放射敏感性与初始DNA损伤相关(r² = 0.92;p = 0.0026),当染色质浓缩改变时这种相关性也成立。实验表明,初始DNA损伤和染色质结构是放射敏感性的主要决定因素。

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