Toyoshima-Sasatani Megumi, Imura Fumika, Hamatake Yuko, Fukunaga Akihiro, Negishi Tomoe
Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan.
Research Institute for Radiation Biology and Medicine, Hiroshima University, Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.
Genes Environ. 2023 Mar 23;45(1):11. doi: 10.1186/s41021-023-00267-4.
Apoptotic cell death is an important survival system for multicellular organisms because it removes damaged cells. Mutation is also a survival method for dealing with damaged cells in multicellular and also unicellular organisms, when DNA lesions are not removed. However, to the best of our knowledge, no reports have comprehensively explored the direct relationship between apoptosis and somatic cell mutations induced by various mutagenic factors.
Mutation was examined by the wing-spot test, which is used to detect somatic cell mutations, including chromosomal recombination. Apoptosis was observed in the wing discs by acridine orange staining in situ. After treatment with chemical mutagens, ultraviolet light (UV), and X-ray, both the apoptotic frequency and mutagenic activity increased in a dose-dependent manner at non-toxic doses. When we used DNA repair-deficient Drosophila strains, the correlation coefficient of the relationship between apoptosis and mutagenicity, differed from that of the wild-type. To explore how apoptosis affects the behavior of mutated cells, we determined the spot size, i.e., the number of mutated cells in a spot. In parallel with an increase in apoptosis, the spot size increased with MNU or X-ray treatment dose-dependently; however, this increase was not seen with UV irradiation. In addition, BrdU incorporation, an indicator of cell proliferation, in the wing discs was suppressed at 6 h, with peak at 12 h post-treatment with X-ray, and that it started to increase again at 24 h; however, this was not seen with UV irradiation.
Damage-induced apoptosis and mutation might be coordinated with each other, and the frequency of apoptosis and mutagenicity are balanced depending on the type of DNA damage. From the data of the spot size and BrdU incorporation, it is possible that mutated cells replace apoptotic cells due to their high frequency of cell division, resulting in enlargement of the spot size after MNU or X-ray treatment. We consider that the induction of mutation, apoptosis, and/or cell growth varies in multi-cellular organisms depending on the type of the mutagens, and that their balance and coordination have an important function to counter DNA damage for the survival of the organism.
细胞凋亡性死亡是多细胞生物重要的生存机制,因为它能清除受损细胞。当DNA损伤未被修复时,突变也是多细胞生物以及单细胞生物应对受损细胞的一种生存方式。然而,据我们所知,尚无报告全面探究细胞凋亡与各种诱变因素诱导的体细胞突变之间的直接关系。
通过用于检测体细胞突变(包括染色体重组)的翅斑试验检测突变情况。通过吖啶橙原位染色在翅盘中观察细胞凋亡。用化学诱变剂、紫外线(UV)和X射线处理后,在无毒剂量下,细胞凋亡频率和诱变活性均呈剂量依赖性增加。当我们使用DNA修复缺陷型果蝇品系时,细胞凋亡与诱变之间关系的相关系数与野生型不同。为了探究细胞凋亡如何影响突变细胞的行为,我们测定了斑点大小,即一个斑点中突变细胞的数量。随着细胞凋亡增加,经N-甲基-N-亚硝基脲(MNU)或X射线处理后,斑点大小呈剂量依赖性增加;然而,紫外线照射未出现这种增加情况。此外,翅盘中细胞增殖指标5-溴脱氧尿嘧啶核苷(BrdU)掺入在X射线处理后6小时受到抑制,12小时达到峰值,24小时又开始增加;然而,紫外线照射未出现这种情况。
损伤诱导的细胞凋亡和突变可能相互协调,细胞凋亡频率和诱变活性根据DNA损伤类型保持平衡。从斑点大小和BrdU掺入数据来看,由于突变细胞的高细胞分裂频率,它们可能取代凋亡细胞,导致MNU或X射线处理后斑点大小增大。我们认为,多细胞生物中突变、细胞凋亡和/或细胞生长的诱导因诱变剂类型而异,它们之间的平衡与协调对于生物生存对抗DNA损伤具有重要作用。