Shi Da, Xu Su, Zhuo Jiachen, McKenna Mary C, Gullapalli Rao P
Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Dev Neurosci. 2019;41(5-6):274-289. doi: 10.1159/000506679. Epub 2020 Apr 29.
Fragile X syndrome (FXS) is the most commonly inherited form of intellectual disability ascribed to the autism spectrum disorder. Studies with FXS patients have reported altered white matter volume compared to controls. The Fmr1 knockout (KO) mouse, a model for FXS, showed evidence of delayed myelination during postnatal brain development. In this study, we examined several white matter regions in the male Fmr1 KO mouse brain compared to male wild-type (WT) mice at postnatal days (PND) 18, 21, 30, and 60, which coincide with critical stages of myelination and postnatal brain development. White matter volume, T2 relaxation time, and magnetization transfer ratio (MTR) were measured using magnetic resonance imaging and myelin content was determined with histological staining of myelin. Differences in the developmental accumulation of white matter and myelin between Fmr1 KO and WT mice were observed in the corpus callosum, external and internal capsules, cerebral peduncle, and fimbria. Alterations were more predominant in the external and internal capsules and fimbria of Fmr1 KO mice, where the MTR was lower at PND 18, then elevated at PND 30, and again lower at PND 60 compared to the corresponding regions in WT mice. The pattern of changes in MTR were similar to those observed in myelin staining and could be related to the altered protein synthesis that is a hallmark of FXS. While no significant changes in white matter volumes and T2 relaxation time between the Fmr1 KO and WT mice were observed, the altered pattern of myelin staining and MTR, particularly in the external capsule, reflecting the abnormalities associated with myelin content is suggestive of a developmental delay in the white matter of Fmr1 KO mouse brain. These early differences in white matter during critical developmental stages may contribute to altered brain networks in the Fmr1 KO mice.
脆性X综合征(FXS)是自闭症谱系障碍中最常见的遗传性智力残疾形式。对FXS患者的研究报告称,与对照组相比,其白质体积发生了改变。Fmr1基因敲除(KO)小鼠是FXS的一种模型,显示出在出生后大脑发育过程中有髓鞘形成延迟的迹象。在本研究中,我们在出生后第18、21、30和60天,将雄性Fmr1 KO小鼠大脑中的几个白质区域与雄性野生型(WT)小鼠进行了比较,这些时间点与髓鞘形成和出生后大脑发育的关键阶段相吻合。使用磁共振成像测量白质体积、T2弛豫时间和磁化传递率(MTR),并用髓鞘组织学染色确定髓鞘含量。在胼胝体、外囊和内囊、大脑脚和伞中观察到Fmr1 KO小鼠和WT小鼠之间白质和髓鞘发育积累的差异。Fmr1 KO小鼠的外囊和内囊以及伞中的变化更为明显,与WT小鼠的相应区域相比,其MTR在出生后第18天较低,在出生后第30天升高,在出生后第60天再次降低。MTR的变化模式与髓鞘染色中观察到的相似,可能与FXS的标志性蛋白质合成改变有关。虽然在Fmr1 KO小鼠和WT小鼠之间未观察到白质体积和T2弛豫时间的显著变化,但髓鞘染色和MTR的改变模式,特别是在外囊中,反映了与髓鞘含量相关的异常,提示Fmr1 KO小鼠大脑白质存在发育延迟。在关键发育阶段白质的这些早期差异可能导致Fmr1 KO小鼠大脑网络的改变。