Department of Radiation Oncology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Cytometry A. 2010 Oct;77(10):940-52. doi: 10.1002/cyto.a.20955. Epub 2010 Aug 18.
Radiosensitization of mammalian cells by heat is believed to involve the inhibition of repair of DNA double-strand breaks (DSBs). The Mre11 complex (composed of Mre11, Rad50, and Nbs1) is involved in DSB repair and forms foci at sites of radiation-induced DSBs. Heat induces the translocation of a significant amount of Mre11, Rad50, and Nbs1 from the nucleus to the cytoplasm, but little is known about how heat affects the integrity of the proteins still remaining in nuclei, or alters kinetics of formation/disappearance of DNA repair foci in heated, irradiated cells. Here, we show that hyperthermia alters the interaction between proteins of the Mre11 complex in irradiated human melanoma cells and inhibits the formation of repair foci. At various times after X-irradiation and/or heating (2 h at 41.5 or 42.5 °C), the cells were fixed and stained for Mre11, Rad50, and Nbs1. Colocalization of proteins and formation and disappearance of nuclear foci in heated and/or irradiated cells, determined using confocal microscopy, were compared. In heated, irradiated cells, focus formation was inhibited for 2-8 h, and colocalization of the proteins of the Mre11 complex was reduced for 12-24 h post-treatment. Colocalization was recovered in irradiated cells within 24 h after heating at 41.5 °C, but was inhibited longer after heating at 42.5 °C. The decreased colocalization in heated, irradiated cells suggests that there is a decrease in protein interaction, and Mre11 complexes in nuclei disassemble after heating. Such changes could be involved, at least in part, in heat radiosensitization and inhibition of DSB repair. Also, the kinetics of disassembly and reassembly of Mre11 complexes appears to be dependent upon treatment temperature.
哺乳动物细胞的热增敏被认为涉及 DNA 双链断裂 (DSB) 的修复抑制。Mre11 复合物(由 Mre11、Rad50 和 Nbs1 组成)参与 DSB 修复,并在辐射诱导的 DSB 部位形成焦点。热诱导大量 Mre11、Rad50 和 Nbs1 从核转移到细胞质,但对于热如何影响仍留在核内的蛋白质的完整性,或者改变加热和辐照细胞中 DNA 修复焦点形成/消失的动力学,知之甚少。在这里,我们表明,高温改变了受辐照的人黑色素瘤细胞中 Mre11 复合物蛋白之间的相互作用,并抑制了修复焦点的形成。在 X 射线照射和/或加热(41.5 或 42.5°C 下 2 小时)后的不同时间,将细胞固定并用 Mre11、Rad50 和 Nbs1 染色。使用共聚焦显微镜比较了加热和/或辐照细胞中蛋白质的共定位以及核焦点的形成和消失。在加热和辐照的细胞中,焦点形成在 2-8 小时内受到抑制,并且在处理后 12-24 小时内 Mre11 复合物的蛋白质共定位减少。在 41.5°C 加热后 24 小时内,辐照细胞中的共定位得到恢复,但在 42.5°C 加热后更长时间受到抑制。加热和辐照细胞中减少的共定位表明蛋白质相互作用减少,并且核内的 Mre11 复合物在加热后解体。这些变化至少部分可能涉及热增敏和 DSB 修复抑制。此外,Mre11 复合物的解体和重组动力学似乎取决于处理温度。