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人类发育过程中皮质微结构的磁共振成像特征与少突胶质细胞类型表达一致。

MRI signatures of cortical microstructure in human development align with oligodendrocyte cell-type expression.

作者信息

Genc Sila, Ball Gareth, Chamberland Maxime, Raven Erika P, Tax Chantal M W, Ward Isobel, Yang Joseph Y M, Palombo Marco, Jones Derek K

机构信息

Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Cardiff, UK.

Developmental Imaging, Clinical Sciences, Murdoch Children's Research Institute, Parkville, VIC, Australia.

出版信息

Nat Commun. 2025 Apr 7;16(1):3317. doi: 10.1038/s41467-025-58604-w.

Abstract

Neuroanatomical changes to the cortex during adolescence have been well documented using MRI, revealing ongoing cortical thinning and volume loss. Recent advances in MRI hardware and biophysical models of tissue informed by diffusion MRI data hold promise for identifying the cellular changes driving these morphological observations. Using ultra-strong gradient MRI, this study quantifies cortical neurite and soma microstructure in typically developing youth. Across domain-specific networks, cortical neurite signal fraction, attributed to neuronal and glial processes, increases with age. The apparent soma radius, attributed to the apparent radius of glial and neuronal cell bodies, decreases with age. Analyses of two independent post-mortem datasets reveal that genes increasing in expression through adolescence are significantly enriched in cortical oligodendrocytes and Layer 5-6 neurons. In our study, we show spatial and temporal alignment of oligodendrocyte cell-type gene expression with neurite and soma microstructural changes, suggesting that ongoing cortical myelination processes drive adolescent cortical development.

摘要

利用磁共振成像(MRI)对青春期皮质的神经解剖学变化已有充分记录,揭示了皮质持续变薄和体积减小。MRI硬件的最新进展以及基于扩散MRI数据的组织生物物理模型有望识别驱动这些形态学观察结果的细胞变化。本研究使用超强梯度MRI对典型发育青年的皮质神经突和胞体微观结构进行了量化。在特定领域的网络中,归因于神经元和神经胶质突起的皮质神经突信号分数随年龄增长而增加。归因于神经胶质和神经元细胞体表观半径的表观胞体半径随年龄减小。对两个独立的死后数据集的分析表明,在青春期表达增加的基因在皮质少突胶质细胞和第5 - 6层神经元中显著富集。在我们的研究中,我们展示了少突胶质细胞类型基因表达与神经突和胞体微观结构变化的时空一致性,表明持续的皮质髓鞘形成过程驱动了青春期皮质发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d0b/11977195/434b97cc3328/41467_2025_58604_Fig1_HTML.jpg

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