Wang Xiaojie, Studholme Colin, Grigsby Peta L, Frias Antonio E, Cuzon Carlson Verginia C, Kroenke Christopher D
Divisions of Neuroscience.
Biomedical Image Computing Group, Departments of Pediatrics, Bioengineering and Radiology, University of Washington, Seattle, Washington 98105, and.
J Neurosci. 2017 Feb 22;37(8):1971-1983. doi: 10.1523/JNEUROSCI.3157-16.2017. Epub 2017 Jan 9.
Altered macroscopic anatomical characteristics of the cerebral cortex have been identified in individuals affected by various neurodevelopmental disorders. However, the cellular developmental mechanisms that give rise to these abnormalities are not understood. Previously, advances in image reconstruction of diffusion magnetic resonance imaging (MRI) have made possible high-resolution measurements of water diffusion anisotropy in the fetal brain. Here, diffusion anisotropy within the developing fetal cerebral cortex is longitudinally characterized in the rhesus macaque, focusing on gestation day (G85) through G135 of the 165 d term. Additionally, for subsets of animals characterized at G90 and G135, immunohistochemical staining was performed, and 3D structure tensor analyses were used to identify the cellular processes that most closely parallel changes in water diffusion anisotropy with cerebral cortical maturation. Strong correlations were found between maturation of dendritic arbors on the cellular level and the loss of diffusion anisotropy with cortical development. In turn, diffusion anisotropy changes were strongly associated both regionally and temporally with cortical folding. Notably, the regional and temporal dependence of diffusion anisotropy and folding were distinct from the patterns observed for cerebral cortical surface area expansion. These findings strengthen the link proposed in previous studies between cellular-level changes in dendrite morphology and noninvasive diffusion MRI measurements of the developing cerebral cortex and support the possibility that, in gyroencephalic species, structural differentiation within the cortex is coupled to the formation of gyri and sulci. Abnormal brain morphology has been found in populations with neurodevelopmental disorders. However, the mechanisms linking cellular level and macroscopic maturation are poorly understood, even in normal brains. This study contributes new understanding to this subject using serial MRI measurements of rhesus macaque fetuses, from which macroscopic and cellular information can be derived. We found that morphological differentiation of dendrites was strongly associated both regionally and temporally with folding of the cerebral cortex. Interestingly, parallel associations were not observed with cortical surface area expansion. These findings support the possibility that perturbed morphological differentiation of cells within the cortex may underlie abnormal macroscopic characteristics of individuals affected by neurodevelopmental disorders.
在患有各种神经发育障碍的个体中,已发现大脑皮质的宏观解剖特征发生了改变。然而,导致这些异常的细胞发育机制尚不清楚。此前,扩散磁共振成像(MRI)的图像重建技术进步使得对胎儿大脑中的水扩散各向异性进行高分辨率测量成为可能。在此,对恒河猴发育中的胎儿大脑皮质内的扩散各向异性进行纵向表征,重点关注165天孕期中的妊娠第85天(G85)至第135天。此外,对于在G90和G135进行表征的动物亚组,进行了免疫组织化学染色,并使用三维结构张量分析来识别与大脑皮质成熟过程中最密切平行的水扩散各向异性变化的细胞过程。在细胞水平上,树突分支的成熟与皮质发育过程中扩散各向异性的丧失之间发现了强相关性。反过来,扩散各向异性的变化在区域和时间上都与皮质折叠密切相关。值得注意的是,扩散各向异性和折叠的区域及时间依赖性与大脑皮质表面积扩展所观察到的模式不同。这些发现加强了先前研究中提出的树突形态细胞水平变化与发育中大脑皮质的无创扩散MRI测量之间的联系,并支持了在脑回物种中,皮质内的结构分化与脑回和脑沟形成相关联的可能性。在患有神经发育障碍的人群中发现了异常的脑形态。然而,即使在正常大脑中,将细胞水平与宏观成熟联系起来的机制也知之甚少。本研究通过对恒河猴胎儿进行系列MRI测量,为该主题提供了新的认识,从中可以获得宏观和细胞信息。我们发现树突的形态分化在区域和时间上都与大脑皮质的折叠密切相关。有趣的是,未观察到与皮质表面积扩展的平行关联。这些发现支持了这样一种可能性,即皮质内细胞形态分化的紊乱可能是受神经发育障碍影响个体异常宏观特征背后的原因。