NeuroSpin, Frederic Joliot Institute, Commissariat à l'Energie Atomique, Université Paris- Saclay, Gif-sur-Yvette, France.
Université de Paris and Université Paris-Saclay, Inserm, LRP/iRCM/IBFJ CEA, UMR Stabilité Génétique Cellules Souches et Radiations, F-92265, Fontenay-aux-Roses, France.
Radiat Res. 2021 Jun 1;195(6):568-583. doi: 10.1667/RADE-20-00136.1.
In utero exposure to ionizing radiation can lead to cerebral alterations during adulthood. Using anatomical magnetic resonance imaging (MRI), it is possible to assess radiation-induced structural brain damage noninvasively. However, little is currently known about microstructure alterations in brain tissue. Therefore, the goal of this study was to establish, based on an original and robust pipeline of MRI image analysis, whether the long-term effects of in utero radiation exposure on brain tissue microstructure could be detected noninvasively. Pregnant C57BL/6N mice received a single dose of 1 Gy on gestation day 14.5, which led to behavioral impairments in adults. At 3 months old, in vivo MRI data were acquired from in utero irradiated and nonirradiated male mice. An MRI protocol was designed to assess the effects of radiation on the parameters of brain volume, non-Gaussian diffusion (ADC0, kurtosis and signature index) and anisotropic diffusion (fractional anisotropy and mean, axial, radial diffusivities and anisotropic signature index) in 10 key cerebral structures defined using an in-house atlas of the mouse brain. Based on the relative amplitude of these anatomical and microstructural changes, maps of the radiosensitivity of the brain to in utero irradiation were created. We observed microcephaly in irradiated mice with noticeably larger volume changes in the cortex and the corpus callosum. We also observed significantly lower ADC0, anisotropy fraction (sFA), radial diffusivity (sRD), as well as signature index (S-index and SI3) values, which are original markers sensitive to tissue microstructure alterations. All these changes together are in favor of a decreased cellular "imprint" and in some regions a reduced density in myelinated axons. A reduction in the number and complexity of myelinated axons was further revealed by myelin basic protein immunostaining. Combining anatomical and diffusion MRI is a promising approach to noninvasively investigate the radiosensitivity of local brain areas in adult mice after in utero irradiation in terms of microstructure.
子宫内暴露于电离辐射会导致成年后大脑发生改变。使用解剖磁共振成像(MRI),可以无创地评估辐射引起的结构性脑损伤。然而,目前对于脑组织的微观结构改变知之甚少。因此,本研究的目的是基于原始且稳健的 MRI 图像分析管道,确定是否可以无创地检测到子宫内辐射暴露对脑组织微观结构的长期影响。将怀孕的 C57BL/6N 小鼠在妊娠第 14.5 天接受单次 1 Gy 的照射,这导致成年后出现行为障碍。在 3 个月大时,从子宫内照射和未照射的雄性小鼠中获得体内 MRI 数据。设计了一种 MRI 方案,以评估辐射对 10 个关键脑结构的脑容量、非高斯扩散(ADC0、峰度和特征指数)和各向异性扩散(分数各向异性和平均、轴向、径向扩散率和各向异性特征指数)参数的影响,使用了小鼠大脑的内部图谱来定义这些结构。基于这些解剖和微观结构变化的相对幅度,创建了大脑对子宫内照射的辐射敏感性图。我们观察到照射组小鼠出现了明显的大脑微缩症,其皮质和胼胝体的体积变化明显更大。我们还观察到 ADC0、各向异性分数(sFA)、径向扩散率(sRD)和特征指数(S-index 和 SI3)值显著降低,这些都是对组织微观结构改变敏感的原始标志物。所有这些变化共同表明细胞“印记”减少,在某些区域,少突胶质细胞轴突的密度降低。髓鞘碱性蛋白免疫染色进一步揭示了少突胶质细胞轴突数量和复杂性的减少。结合解剖和扩散 MRI 是一种很有前途的方法,可以无创地研究子宫内照射后成年小鼠局部脑区的微观结构的辐射敏感性。