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小鼠缰核发育过程中的分子特征和细胞多样性。

Molecular signatures and cellular diversity during mouse habenula development.

机构信息

Department of Translational Neuroscience, UMC Utrecht Brain Center, University Medical Center, Utrecht University, 3584 Utrecht, the Netherlands.

Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam, VU University Amsterdam, 1081 Amsterdam, the Netherlands.

出版信息

Cell Rep. 2022 Jul 5;40(1):111029. doi: 10.1016/j.celrep.2022.111029.

Abstract

The habenula plays a key role in various motivated and pathological behaviors and is composed of molecularly distinct neuron subtypes. Despite progress in identifying mature habenula neuron subtypes, how these subtypes develop and organize into functional brain circuits remains largely unknown. Here, we performed single-cell transcriptional profiling of mouse habenular neurons at critical developmental stages, instructed by detailed three-dimensional anatomical data. Our data reveal cellular and molecular trajectories during embryonic and postnatal development, leading to different habenular subtypes. Further, based on this analysis, our work establishes the distinctive functional properties and projection target of a subtype of Cartpt habenula neurons. Finally, we show how comparison of single-cell transcriptional profiles and GWAS data links specific developing habenular subtypes to psychiatric disease. Together, our study begins to dissect the mechanisms underlying habenula neuron subtype-specific development and creates a framework for further interrogation of habenular development in normal and disease states.

摘要

缰核对各种动机和病理性行为起着关键作用,由分子上不同的神经元亚型组成。尽管在鉴定成熟缰核神经元亚型方面取得了进展,但这些亚型如何发育并组织成功能性大脑回路在很大程度上仍不清楚。在这里,我们根据详细的三维解剖数据,对关键发育阶段的小鼠缰核神经元进行了单细胞转录组分析。我们的数据揭示了胚胎和出生后发育过程中的细胞和分子轨迹,导致了不同的缰核亚型。此外,基于这项分析,我们的工作确立了一种 Cartpt 缰核神经元亚型的独特功能特性和投射靶标。最后,我们展示了如何将单细胞转录组分析和 GWAS 数据进行比较,将特定的发育中的缰核亚型与精神疾病联系起来。总之,我们的研究开始剖析缰核神经元亚型特异性发育的机制,并为进一步研究正常和疾病状态下缰核的发育奠定了框架。

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