Radiation Physiology Laboratory, Singapore Nuclear Research and Safety Initiative, National University of Singapore, Singapore.
Cells. 2024 Oct 15;13(20):1705. doi: 10.3390/cells13201705.
Our previous study demonstrated that the acute high-dose-rate (3.3 Gy/min) γ-ray irradiation (γ-irradiation) of postnatal day-3 (P3) mice with 5 Gy induced depression and drastic neuropathological changes in the dentate gyrus of the hippocampus of adult mice. The present study investigated the effects of chronic low-dose-rate (1.2 mGy/h) γ-irradiation from P3 to P180 with a cumulative dose of 5 Gy on animal behaviour, hippocampal cellular change, and miRNA and mRNA expression in the hippocampus and blood in female mice. The radiation exposure did not significantly affect the animal's body weight, and neuropsychiatric changes such as anxiety and depression were examined by neurobehavioural tests, including open field, light-dark box, elevated plus maze, tail suspension, and forced swim tests. Immunohistochemical staining did not detect any obvious loss of mature and immature neurons (NeuN and DCX) or any inflammatory glial response (IBA1, GFAP, and PDGFRα). Nevertheless, γH2AX foci in the stratum granulosum of the dentate gyrus were significantly increased, suggesting the chronic low-dose-rate irradiation induced persistent DNA damage foci in mice. miRNA sequencing and qRT-PCR indicated an increased expression of miR-448-3p and miR-361-5p but decreased expression of miR-193a-3p in the mouse hippocampus. Meanwhile, mRNA sequencing and qRT-PCR showed the changed expression of some genes, including , , and . Database searching by miRDB and TargetScan predicted that and are the targets of miR-448-3p, and is the target of miR-361-5p. miRNA/mRNA sequencing and qRT-PCR results in blood showed the increased expression of miR-6967-3p and the decreased expression of its target . The interactions of these miRNAs and mRNAs may be related to the chronic low-dose-rate radiation-induced persistent DNA damage.
我们之前的研究表明,对出生后第 3 天(P3)的小鼠进行 5 Gy 的急性高剂量率(3.3 Gy/min)γ 射线照射(γ 照射)会导致成年小鼠海马齿状回的抑郁和严重的神经病理学变化。本研究调查了从 P3 到 P180 进行慢性低剂量率(1.2 mGy/h)γ 照射(累积剂量为 5 Gy)对雌性小鼠的动物行为、海马细胞变化以及海马和血液中 microRNA 和 mRNA 表达的影响。辐射暴露对动物体重没有显著影响,通过神经行为测试,包括旷场、明暗箱、高架十字迷宫、悬尾和强迫游泳测试,检测焦虑和抑郁等神经精神变化。免疫组织化学染色未检测到成熟和未成熟神经元(NeuN 和 DCX)或任何炎症性神经胶质反应(IBA1、GFAP 和 PDGFRα)的明显丢失。然而,齿状回颗粒层中的 γH2AX 焦点明显增加,表明慢性低剂量率照射诱导了小鼠持续的 DNA 损伤焦点。miRNA 测序和 qRT-PCR 表明,小鼠海马中 miR-448-3p 和 miR-361-5p 的表达增加,但 miR-193a-3p 的表达减少。同时,mRNA 测序和 qRT-PCR 显示了一些基因的表达变化,包括、和。miRDB 和 TargetScan 的数据库搜索预测和是 miR-448-3p 的靶基因,是 miR-361-5p 的靶基因。miRNA/mRNA 测序和 qRT-PCR 结果显示血液中 miR-6967-3p 的表达增加,其靶基因的表达减少。这些 miRNA 和 mRNAs 的相互作用可能与慢性低剂量率辐射诱导的持续 DNA 损伤有关。