Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino, 142290 Moscow, Russia.
Joint Institute for Nuclear Research, Dubna, 141980 Moscow, Russia.
Int J Mol Sci. 2020 Feb 11;21(4):1196. doi: 10.3390/ijms21041196.
Studies of molecular changes occurred in various brain regions after whole-body irradiation showed a significant increase in terms of the importance in gaining insight into how to slow down or prevent the development of long-term side effects such as carcinogenesis, cognitive impairment and other pathologies. We have analyzed nDNA damage and repair, changes in mitochondrial DNA (mtDNA) copy number and in the level of mtDNA heteroplasmy, and also examined changes in the expression of genes involved in the regulation of mitochondrial biogenesis and dynamics in three areas of the rat brain (hippocampus, cortex and cerebellum) after whole-body X-ray irradiation. Long amplicon quantitative polymerase chain reaction (LA-QPCR) was used to detect nDNA and mtDNA damage. The level of mtDNA heteroplasmy was estimated using Surveyor nuclease technology. The mtDNA copy numbers and expression levels of a number of genes were determined by real-time PCR. The results showed that the repair of nDNA damage in the rat brain regions occurs slowly within 24 h; in the hippocampus, this process runs much slower. The number of mtDNA copies in three regions of the rat brain increases with a simultaneous increase in mtDNA heteroplasmy. However, in the hippocampus, the copy number of mutant mtDNAs increases significantly by the time point of 24 h after radiation exposure. Our analysis shows that in the brain regions of irradiated rats, there is a decrease in the expression of genes (ND2, CytB, ATP5O) involved in ATP synthesis, although by the same time point after irradiation, an increase in transcripts of genes regulating mitochondrial biogenesis is observed. On the other hand, analysis of genes that control the dynamics of mitochondria (Mfn1, Fis1) revealed that sharp decrease in gene expression level occurred, only in the hippocampus. Consequently, the structural and functional characteristics of the hippocampus of rats exposed to whole-body radiation can be different, most significantly from those of the other brain regions.
对全身照射后不同脑区发生的分子变化的研究表明,深入了解如何减缓或预防致癌作用、认知障碍和其他病变等长期副作用的发展具有重要意义。我们分析了 nDNA 损伤和修复、线粒体 DNA(mtDNA)拷贝数和 mtDNA 异质性水平的变化,还检查了全身 X 射线照射后大鼠脑三个区域(海马体、皮质和小脑)中线粒体生物发生和动力学调节基因表达的变化。长扩增子定量聚合酶链反应(LA-QPCR)用于检测 nDNA 和 mtDNA 损伤。Surveyor 核酸内切酶技术用于估计 mtDNA 异质性水平。通过实时 PCR 确定 mtDNA 拷贝数和一些基因的表达水平。结果表明,大鼠脑区 nDNA 损伤的修复在 24 h 内缓慢发生;在海马体中,这个过程进行得更慢。大鼠脑三个区域的 mtDNA 拷贝数随着 mtDNA 异质性的同时增加而增加。然而,在海马体中,辐射暴露 24 h 后,突变型 mtDNA 的拷贝数显著增加。我们的分析表明,在照射大鼠的脑区中,参与 ATP 合成的基因(ND2、CytB、ATP5O)表达减少,尽管在同一时间点后,调节线粒体生物发生的基因转录增加。另一方面,分析控制线粒体动力学的基因(Mfn1、Fis1)表明,基因表达水平急剧下降,仅在海马体中发生。因此,全身辐射暴露后大鼠海马体的结构和功能特征可能与其他脑区有很大不同。