Transcriptomic profiles link corticostriatal microarchitecture to genetics of neurodevelopment and neuropsychiatric risks.

IF 6.2 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-02-11 DOI:10.1038/s41398-025-03260-3
Sheng Hu, Yanming Wang, Xiaoxiao Wang, Yang Ji, Chuanfu Li, Bensheng Qiu
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Abstract

Many studies on macroscale organization have focused on only the cerebral cortex or striatum, leaving a large gap in the microstructural gradient of corticostriatal covariance. Here, we partitioned the striatum into seven distinct parcels and computed the microstructural covariance between each parcel and the cerebral cortex using T1-weighted/T2-weighted mapping. We found that corticostriatal microstructural covariance exhibited a microstructural gradient along the anterior-posterior axis of the striatum. The patterns of corticostriatal microstructural covariance are linked to geodesic distance and cell type-specific gene expression profiles, revealing a gradually attenuated relationship along the anterior-posterior axis of the striatum. Linking gene expression profile to corticostriatal microstructural patterns showed that the transcriptional variations in cell type-specific genes are different between the anterior and posterior striatum and suggested that anterior striatum are more enriched in psychiatric disorders. Moreover, at the genetic level, the corticostriatal microarchitecture showed a spatiotemporal trait during neurodevelopment. Finally, we identified the neural circuits from limbic and medial frontal cortex to striatum that contributes to the common neuropsychiatric disorders. Collectively, our findings reveal spatially covarying of transcriptional specializations with microarchitecture of corticostriatal covariance, highlighting the mechanisms underlying that neurodevelopmental corticostriatal circuits may be involved in neuropsychiatric disorders.

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转录组谱将皮质纹状体微结构与神经发育和神经精神风险的遗传学联系起来。
许多关于宏观组织的研究只关注大脑皮层或纹状体,在皮层纹状体协方差的微观结构梯度上有很大的空白。在这里,我们将纹状体划分为七个不同的包裹,并使用t1加权/ t2加权映射计算每个包裹与大脑皮层之间的微观结构协方差。我们发现皮质纹状体微结构协方差沿纹状体前后轴呈现微结构梯度。皮质纹状体微观结构协方差的模式与测地线距离和细胞类型特异性基因表达谱有关,揭示了纹状体前后轴的关系逐渐减弱。将基因表达谱与皮质纹状体微观结构模式联系起来表明,细胞类型特异性基因的转录变异在前纹状体和后纹状体之间是不同的,这表明前纹状体在精神疾病中更丰富。此外,在遗传水平上,皮质纹状体微结构在神经发育过程中表现出时空特征。最后,我们确定了从边缘和内侧额叶皮层到纹状体的神经回路,这些神经回路有助于常见的神经精神疾病。总的来说,我们的研究结果揭示了转录特化的空间共变与皮质纹状体协方差的微结构,突出了神经发育皮质纹状体回路可能参与神经精神疾病的潜在机制。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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