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放射敏感性相关的 microRNA-34a-5p 水平变化及其在小鼠出生后 10 天和 21 天照射后齿状回门区神经元丢失的关系。

Radiosensitivity-related Variation in MicroRNA-34a-5p Levels and Subsequent Neuronal Loss in the Hilus of the Dentate Gyrus after Irradiation at Postnatal Days 10 and 21 in Mice.

机构信息

The School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, Hubei 434023, China.

Radiation Physiology Laboratory, Singapore Nuclear Research and Safety Initiative, National University of Singapore, 138602, Singapore.

出版信息

Radiat Res. 2024 Oct 1;202(4):677-684. doi: 10.1667/RADE-23-00248.1.

Abstract

The radiosensitivity of mice differs between postnatal days 10 (P10) and 21(P21); these days mark different stages of brain development. In the present study, Ki67 and doublecotin (DCX) immunostaining and hematoxylin staining was performed, which showed that acute radiation exposure at postnatal day 10 induced higher cell apoptosis and loss in the hilus of the dentate gyrus at day 1 postirradiation than postnatal day 21. MicroRNA (miRNA) sequencing and real-time quantitative reverse transcription PCR (qRT-PCR) analysis indicated the upregulation of miRNA-34a-5p at days 1 and 7 after irradiation at postnatal day 10, but not at postnatal day 21. Down-regulation of T-cell intracytoplasmic antigen-1 pathway (Tia1) was indicated by qRT-PCR at day 1 day but not day 7 after irradiation at postnatal day 10. Neurobehavioral testing in mature mice irradiated at postnatal day 10 demonstrated the impairment of short-term memory in novel object recognition and spatial memory, compared to those irradiated at postnatal day 21. Combined with our previous luciferase assay showing the direct interaction of miRNA34a-5p and Tia1, these findings suggest that radiation-induced abnormal miR-34a-5p/Tial interaction at day 1 after irradiation at postnatal day 10 may be involved in apoptosis of the dentate gyrus hilar, impairment of neurogenesis and subsequent short-term memory loss as observed in the novel object recognition and Barnes maze tests.

摘要

在出生后第 10 天(P10)和第 21 天(P21)之间,小鼠的放射敏感性存在差异;这两天标志着大脑发育的不同阶段。在本研究中,进行了 Ki67 和 doublecotin(DCX)免疫染色和苏木精染色,结果表明,在 P10 天的急性辐射暴露后,在辐射后第 1 天诱导了更高的细胞凋亡和齿状回门区的丧失,而在 P21 天则没有。微 RNA(miRNA)测序和实时定量逆转录 PCR(qRT-PCR)分析表明,在 P10 天的照射后第 1 天和第 7 天,miRNA-34a-5p 上调,但在 P21 天则没有。qRT-PCR 显示,在 P10 天照射后第 1 天,但不是第 7 天,T 细胞胞浆抗原-1 通路(Tia1)下调。在 P10 天照射后的成熟小鼠中进行的神经行为测试表明,与 P21 天照射相比,新物体识别和空间记忆的短期记忆受损。结合我们之前的荧光素酶测定结果表明,miRNA34a-5p 和 Tia1 的直接相互作用,这些发现表明,在 P10 天照射后第 1 天诱导的异常 miR-34a-5p/Tial 相互作用可能参与了齿状回门区的凋亡、神经发生的受损以及随后在新物体识别和 Barnes 迷宫测试中观察到的短期记忆丧失。

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