Department of Medical Bioscience, University of the Western Cape, Faculty of Science, Robert Sobukwe Road, Bellville, Cape Town, 7535, South Africa.
Nuclear Medicine Department, Radiation Biophysics Division, NRF-iThemba LABS, Old Faure Road, Faure, Cape Town, 7131, South Africa.
Sci Rep. 2021 Oct 21;11(1):20854. doi: 10.1038/s41598-021-00229-2.
The radiosensitivity of haematopoietic stem and progenitor cells (HSPCs) to neutron radiation remains largely underexplored, notwithstanding their potential role as target cells for radiation-induced leukemogenesis. New insights are required for radiation protection purposes, particularly for aviation, space missions, nuclear accidents and even particle therapy. In this study, HSPCs (CD34CD38 cells) were isolated from umbilical cord blood and irradiated with Co γ-rays (photons) and high energy p(66)/Be(40) neutrons. At 2 h post-irradiation, a significantly higher number of 1.28 ± 0.12 γ-H2AX foci/cell was observed after 0.5 Gy neutrons compared to 0.84 ± 0.14 foci/cell for photons, but this decreased to similar levels for both radiation qualities after 18 h. However, a significant difference in late apoptosis was observed with Annexin-V/PI assay between photon and neutron irradiation at 18 h, 43.17 ± 6.10% versus 55.55 ± 4.87%, respectively. A significant increase in MN frequency was observed after both 0.5 and 1 Gy neutron irradiation compared to photons illustrating higher levels of neutron-induced cytogenetic damage, while there was no difference in the nuclear division index between both radiation qualities. The results point towards a higher induction of DNA damage after neutron irradiation in HSPCs followed by error-prone DNA repair, which contributes to genomic instability and a higher risk of leukemogenesis.
造血干细胞和祖细胞(HSPCs)对中子辐射的放射敏感性在很大程度上仍未得到充分探索,尽管它们可能是辐射诱导白血病发生的靶细胞。为了辐射防护的目的,特别是对于航空、太空任务、核事故甚至粒子治疗,需要新的见解。在这项研究中,从脐带血中分离出 HSPCs(CD34CD38 细胞),并用 Co γ 射线(光子)和高能 p(66)/Be(40)中子进行照射。在照射后 2 小时,与光子照射(0.84±0.14 焦点/细胞)相比,0.5 Gy 中子照射后观察到的 1.28±0.12 γ-H2AX 焦点/细胞数量显著增加,但在 18 小时后,两种辐射质量的焦点数量均下降至相似水平。然而,在 18 小时时,通过 Annexin-V/PI 测定法在光子和中子照射之间观察到晚期凋亡有显著差异,分别为 43.17±6.10%和 55.55±4.87%。与光子照射相比,在接受 0.5 和 1 Gy 中子照射后均观察到 MN 频率显著增加,表明中子诱导的细胞遗传学损伤水平更高,而两种辐射质量之间的核分裂指数没有差异。这些结果表明,HSPCs 中的 DNA 损伤在中子照射后更容易发生,随后是易错的 DNA 修复,这导致基因组不稳定和白血病发生的风险增加。