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转录谱分析与原位表达图像分析相结合,揭示腹侧被盖区 GABA 神经元亚群中镶嵌表达的分子标记物。

Transcriptional profiling aligned with in situ expression image analysis reveals mosaically expressed molecular markers for GABA neuron sub-groups in the ventral tegmental area.

机构信息

MRC London Institute of Medical Sciences (LMS), London, UK.

Institute of Clinical Sciences (ICS), Faculty of Medicine, Imperial College London, London, UK.

出版信息

Eur J Neurosci. 2019 Dec;50(11):3732-3749. doi: 10.1111/ejn.14534. Epub 2019 Aug 16.

DOI:10.1111/ejn.14534
PMID:31374129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6972656/
Abstract

γ-Aminobutyric acid (GABA) neurons in the ventral tegmental area (VTA) provide local inhibitory control of dopamine neuron activity and send long-range projections to several target regions including the nucleus accumbens. They play diverse roles in reward and aversion, suggesting that they be comprised of several functionally distinct sub-groups, but our understanding of this diversity has been limited by a lack of molecular markers that might provide genetic entry points for cell type-specific investigations. To address this, we conducted transcriptional profiling of GABA neurons and dopamine neurons using immunoprecipitation of tagged polyribosomes (RiboTag) and RNAseq. First, we directly compared these two transcriptomes in order to obtain a list of genes enriched in GABA neurons compared with dopamine neurons. Next, we created a novel bioinformatic approach, that used the PANTHER (Protein ANalysis THrough Evolutionary Relationships) gene ontology database and VTA gene expression data from the Allen Mouse Brain Atlas, from which we obtained 6 candidate genes: Cbln4, Rxfp3, Rora, Gpr101, Trh and Nrp2. As a final step, we verified the selective expression of these candidate genes in sub-groups of GABA neurons in the VTA (and neighbouring substantia nigra pars compacta) using immunolabelling. Taken together, our study provides a valuable toolbox for the future investigation of GABA neuron sub-groups in the VTA.

摘要

γ-氨基丁酸 (GABA) 神经元位于腹侧被盖区 (VTA),对多巴胺神经元活动提供局部抑制性控制,并向包括伏隔核在内的多个靶区发出长程投射。它们在奖赏和厌恶中发挥着多样化的作用,这表明它们可能由几个功能上不同的亚群组成,但我们对这种多样性的理解受到缺乏分子标记的限制,这些标记可能为特定于细胞类型的研究提供遗传切入点。为了解决这个问题,我们使用标记多核糖体 (RiboTag) 和 RNAseq 对 GABA 神经元和多巴胺神经元进行了转录谱分析。首先,我们直接比较了这两个转录组,以获得与多巴胺神经元相比在 GABA 神经元中富集的基因列表。接下来,我们创建了一种新的生物信息学方法,该方法使用 PANTHER(通过进化关系进行蛋白质分析)基因本体数据库和来自 Allen 鼠脑图谱的 VTA 基因表达数据,从中我们获得了 6 个候选基因:Cbln4、Rxfp3、Rora、Gpr101、Trh 和 Nrp2。作为最后一步,我们使用免疫标记法验证了这些候选基因在 VTA(和邻近的黑质致密部)中 GABA 神经元亚群中的选择性表达。总之,我们的研究为未来研究 VTA 中的 GABA 神经元亚群提供了一个有价值的工具箱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/2d250ff8f7b9/EJN-50-3732-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/7db43f26a19a/EJN-50-3732-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/c9cec6fc13be/EJN-50-3732-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/c197c7595f47/EJN-50-3732-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/9e8a13aff9c3/EJN-50-3732-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/0a1b3a0b5962/EJN-50-3732-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/d893d80f1cfc/EJN-50-3732-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/21e571ebc95f/EJN-50-3732-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/2d250ff8f7b9/EJN-50-3732-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/7db43f26a19a/EJN-50-3732-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/c9cec6fc13be/EJN-50-3732-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/c197c7595f47/EJN-50-3732-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/9e8a13aff9c3/EJN-50-3732-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/0a1b3a0b5962/EJN-50-3732-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/d893d80f1cfc/EJN-50-3732-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/21e571ebc95f/EJN-50-3732-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8b/6972656/2d250ff8f7b9/EJN-50-3732-g008.jpg

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