从童年到青春期的多尺度大脑结构重组与大脑皮层形态成熟和功能特化相关。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
Yirong He, Debin Zeng, Qiongling Li, Lei Chu, Xiaoxi Dong, Xinyuan Liang, Lianglong Sun, Xuhong Liao, Tengda Zhao, Xiaodan Chen, Tianyuan Lei, Weiwei Men, Yanpei Wang, Daoyang Wang, Mingming Hu, Zhiying Pan, Haibo Zhang, Ningyu Liu, Shuping Tan, Jia-Hong Gao, Shaozheng Qin, Sha Tao, Qi Dong, Yong He, Shuyu Li
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引用次数: 0

摘要

从童年到青春期,人类大脑的结构组织在从突触到宏观白质通路的多个尺度上经历了动态和区域异质性的变化。然而,在此期间,多尺度结构结构的发育过程、与皮质形态变化的关系以及在功能组织成熟中的作用在很大程度上仍然未知。本研究利用6-14岁儿童的两个独立的多模态成像发育数据集,通过构建一个体内多尺度结构连接体模型,结合白质束状图、皮质-皮质邻近性和微观结构相似性,研究了多尺度皮层组织的发育过程。采用梯度映射方法,从多尺度结构连接体中得到的主梯度有效地再现了感觉关联轴。我们的研究结果表明,在发育过程中,多尺度结构梯度空间不断扩大,其特征是主要梯度上初级感觉区和高阶跨模区之间的分化增强。这种与年龄相关的分化与皮质形态的区域异质性变化相平行。此外,多尺度结构连接与功能连接耦合的发展变化与功能专业化细化相关,这可以通过参与系数的变化来证明。值得注意的是,主要多尺度结构梯度的分化与认知能力的提高有关,如工作记忆和注意力表现的增强,并可能受到突触和激素相关生物过程的支持。这些发现促进了我们对复杂的大脑结构组织成熟过程及其对认知表现的影响的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The multiscale brain structural re-organization that occurs from childhood to adolescence correlates with cortical morphology maturation and functional specialization.

From childhood to adolescence, the structural organization of the human brain undergoes dynamic and regionally heterogeneous changes across multiple scales, from synapses to macroscale white matter pathways. However, during this period, the developmental process of multiscale structural architecture, its association with cortical morphological changes, and its role in the maturation of functional organization remain largely unknown. Here, using two independent multimodal imaging developmental datasets aged 6-14 years, we investigated developmental process of multiscale cortical organization by constructing an in vivo multiscale structural connectome model incorporating white matter tractography, cortico-cortical proximity, and microstructural similarity. By employing the gradient mapping method, the principal gradient derived from the multiscale structural connectome effectively recapitulated the sensory-association axis. Our findings revealed a continuous expansion of the multiscale structural gradient space during development, characterized by enhanced differentiation between primary sensory and higher-order transmodal regions along the principal gradient. This age-related differentiation paralleled regionally heterogeneous changes in cortical morphology. Furthermore, the developmental changes in coupling between multiscale structural and functional connectivity were correlated with functional specialization refinement, as evidenced by changes in the participation coefficient. Notably, the differentiation of the principal multiscale structural gradient was associated with improved cognitive abilities, such as enhanced working memory and attention performance, and potentially underpinned by synaptic and hormone-related biological processes. These findings advance our understanding of the intricate maturation process of brain structural organization and its implications for cognitive performance.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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