Shared functional organization between pulvinar-cortical and cortico-cortical connectivity and its structural and molecular imaging correlates.

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-10-13 DOI:10.7554/eLife.100937
Gianpaolo Antonio Basile, Augusto Ielo, Lilla Bonanno, Antonio Cerasa, Giuseppe Santoro, Demetrio Milardi, Giuseppe Pio Anastasi, Ambra Torre, Sergio Baldari, Riccardo Laudicella, Michele Gaeta, Marina Quartu, Maria Pina Serra, Marcello Trucas, Angelo Quartarone, Manojkumar Saranathan, Alberto Cacciola
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引用次数: 0

Abstract

The pulvinar, the largest thalamic nucleus, is a highly interconnected structure supporting perception, visuospatial attention, and emotional processing. Such a central role relies on a precise topographical organization reflected in anatomical connectivity and neurochemical markers. Traditionally subdivided into distinct subnuclei, recent work shows that these divisions only partially explain its organization, which is better captured by continuous gradients of cortical connections along dorso-ventral and medio-lateral axes. While well studied in primates, this gradient-based architecture remains less explored in humans. The present work combines high-quality, multimodal structural and functional imaging with a whole-brain, large-scale, PET atlas mapping 19 neurotransmitter systems. By applying diffusion embedding to tractography, functional connectivity, and receptor coexpression, we identify multiple gradients of structural connections, functional coactivation, and molecular binding patterns. These converge on a shared representation along the dorso-ventral and medio-lateral axes of the human pulvinar, aligning with connectivity transitions from lower-level to higher-order cortical regions. Moreover, this is paralleled by gradual changes in the expression of molecular markers associated with key neuromodulator systems, including serotoninergic, noradrenergic, dopaminergic, and opioid systems. Our findings advance the understanding of pulvinar anatomy and function, offering an exploratory framework to investigate the role of this structure in both health and disease.

枕核-皮质和皮质-皮质连接的共享功能组织及其结构和分子成像相关性。
枕核是最大的丘脑核,是一个高度互联的结构,支持感知、视觉空间注意和情绪处理。这种中心作用依赖于精确的地形组织,反映在解剖连通性和神经化学标志物上。传统上被细分为不同的亚核,最近的研究表明,这些划分只能部分解释其组织,这可以通过皮层连接沿背腹轴和中外侧轴的连续梯度来更好地捕捉。虽然在灵长类动物中得到了很好的研究,但这种基于梯度的结构在人类中仍然很少被探索。目前的工作结合了高质量,多模态结构和功能成像与全脑,大规模,PET图谱绘制19个神经递质系统。通过将扩散嵌入技术应用于神经束成像、功能连接和受体共表达,我们确定了结构连接、功能共激活和分子结合模式的多个梯度。这些信号沿着人类枕核的背腹轴和中外侧轴汇聚在一个共同的表征上,与从低级皮质区域到高级皮质区域的连通性转换一致。此外,与关键神经调节系统(包括血清素能、去甲肾上腺素能、多巴胺能和阿片系统)相关的分子标记物表达的逐渐变化也与此平行。我们的研究结果促进了对髋臼解剖和功能的理解,为研究该结构在健康和疾病中的作用提供了一个探索性框架。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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