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转录因子Pou3f1揭示了小鼠谷氨酸能小脑核神经元的发育和分子多样性。

The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the Mouse.

作者信息

Wu Joshua Po Han, Yeung Joanna, Rahimi-Balaei Maryam, Wu Sih-Rong, Zoghbi Huda, Goldowitz Dan

机构信息

Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.

Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, United States.

出版信息

Front Mol Neurosci. 2022 Jul 20;15:921901. doi: 10.3389/fnmol.2022.921901. eCollection 2022.

DOI:10.3389/fnmol.2022.921901
PMID:35935334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9347289/
Abstract

The cerebellar nuclear (CN) neurons are a molecularly heterogeneous population whose specification into the different cerebellar nuclei is defined by the expression of varying sets of transcription factors. Here, we present a novel molecular marker, Pou3f1, that delineates specific sets of glutamatergic CN neurons. The glutamatergic identity of Pou3f1 cells was confirmed by: (1) the co-expression of vGluT2, a cell marker of glutamatergic neurons; (2) the lack of co-expression between Pou3f1 and GAD67, a marker of GABAergic neurons; (3) the co-expression of Atoh1, the master regulator required for the production of all cerebellar glutamatergic lineages; and (4) the absence of Pou3f1-expressing cells in the -null cerebellum. Furthermore, the lack of Pax6 and Tbr1 expression in Pou3f1 cells reveals that Pou3f1-expressing CN neurons specifically settle in the interposed and dentate nuclei. In addition, the Pou3f1-labeled glutamatergic CN neurons can be further classified by the expression of Brn2 and Irx3. The results of the present study align with previous findings highlighting that the survival of the interposed and dentate CN neurons is largely independent of Pax6. More importantly, the present study extends the field's collective knowledge of the molecular diversity of cerebellar nuclei.

摘要

小脑核(CN)神经元是一个分子异质性群体,其分化为不同的小脑核是由不同转录因子组合的表达所定义的。在这里,我们提出了一种新的分子标记物Pou3f1,它可以描绘出特定组的谷氨酸能CN神经元。Pou3f1细胞的谷氨酸能特性通过以下方式得到证实:(1)谷氨酸能神经元的细胞标记物vGluT2的共表达;(2)Pou3f1与GABA能神经元的标记物GAD67之间缺乏共表达;(3)Atoh1的共表达,Atoh1是所有小脑谷氨酸能谱系产生所需的主要调节因子;(4)在Pax6基因敲除的小脑中不存在表达Pou3f1的细胞。此外,Pou3f1细胞中缺乏Pax6和Tbr1表达表明,表达Pou3f1的CN神经元特异性地定位于间位核和齿状核。此外,Pou3f1标记的谷氨酸能CN神经元可以通过Brn2和Irx3的表达进一步分类。本研究结果与之前的研究结果一致,这些研究结果强调间位核和齿状核CN神经元的存活在很大程度上独立于Pax6。更重要的是,本研究扩展了该领域对小脑核分子多样性的总体认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af20/9347289/de7db0a0291f/fnmol-15-921901-g0010.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af20/9347289/b8be1660c36b/fnmol-15-921901-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af20/9347289/6c98ae233f44/fnmol-15-921901-g0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af20/9347289/e6cf7f470f85/fnmol-15-921901-g0008.jpg
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