孤立束核的分子本体

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Silvia Gasparini, Gislaine Almeida-Pereira, Ana Sofia Peraza Munuzuri, Jon M. Resch, Joel C. Geerling
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引用次数: 0

摘要

孤立束核(NTS)接收内脏信息并调节食欲、消化和心肺系统。在NTS中,不同的过程并行运作以维持生命,但我们对其细胞组成的了解尚不完整。在这里,我们整合了组织学和转录组学分析来识别和比较区分这一大脑区域神经元的分子特征。NTS和后脑区的大多数谷氨酸能神经元共同表达转录因子Lmx1b和Phox2b,但远尾侧NTS的腹侧神经元除外,其中包括产生胰高血糖素样肽1 (GLP-1)的表达cg的神经元。gaba能中间神经元通过Lmx1b+Phox2b大群混合,密集的gaba能神经元簇围绕NTS。Lmx1b+Phox2b大群体包括不同分布的亚群体,表达Grp、Hsd11b2、Npff、Pdyn、Pou3f1、Sctr、Th等标记。这些发现强调了Lmx1b-Phox2b共表达是NTS中谷氨酸能神经元的共同特征,并提高了我们对这一关键脑区神经元组织和分布的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Ontology of the Nucleus of Solitary Tract

Molecular Ontology of the Nucleus of Solitary Tract

The nucleus of the solitary tract (NTS) receives visceral information and regulates appetitive, digestive, and cardiorespiratory systems. Within the NTS, diverse processes operate in parallel to sustain life, but our understanding of their cellular composition is incomplete. Here, we integrate histologic and transcriptomic analysis to identify and compare molecular features that distinguish neurons in this brain region. Most glutamatergic neurons in the NTS and area postrema co-express the transcription factors Lmx1b and Phox2b, except for a ventral band of neurons in the far-caudal NTS, which include the Gcg-expressing neurons that produce glucagon-like peptide 1 (GLP-1). GABAergic interneurons intermingle through the Lmx1b+Phox2b macropopulation, and dense clusters of GABAergic neurons surround the NTS. The Lmx1b+Phox2b macropopulation includes subpopulations with distinct distributions expressing Grp, Hsd11b2, Npff, Pdyn, Pou3f1, Sctr, Th, and other markers. These findings highlight Lmx1bPhox2b co-expression as a common feature of glutamatergic neurons in the NTS and improve our understanding of the organization and distribution of neurons in this critical brain region.

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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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