Dopaminergic Neurons in the Zebrafish Subpallium Belong to the Extended Medial Amygdala

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Daniel Armbruster, Thomas Mueller, Wolfgang Driever
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Abstract

The amygdala is a heterogeneous, multinuclear telencephalic structure critical for motivated and emotion-related behaviors in vertebrates. In ray-finned fish (Actinopterygii) like the teleost zebrafish, a telencephalic outward-growing process called eversion makes defining amygdaloid territories particularly challenging. Teleosts are also peculiar in that they develop numerous dopaminergic (DA) neurons in the subpallium, while in tetrapods, such populations are less prominent or appear only transiently. To shed light on the organization of the amygdala in teleosts, we pursued an evolutionary developmental approach focusing on the topological origin of subpallial DA neurons. Specifically, we analyzed the distribution of tyrosine hydroxylase (Th) in conjunction with expression patterns of pax6a+b, isl1a, nkx2.1, lhx8a, otpa+b, and calb2a as markers of different telencephalic subdivisions in brains of 5- and 30-day-old zebrafish (Danio rerio, Teleostei). Our data show that the previously identified dorsalmost division of the ventral telencephalon (Vdd) needs to be subdivided into an anteroventral pax6a/b-positive portion (Vdd1) and a posterodorsal pax6a/b-negative portion (Vdd2). This pax6a-negative Vdd2 portion develops into the extended medial amygdala (EMeA), including the DA population adjacent to the pallial–subpallial border. Our results also show that the EMeA DA neurons form a heterogeneous group of amygdaloid neurons because they differentially express calb2a and sst7. Our work sheds light on the early evolution and development of the amygdala and provides a foundation for functional analysis of the newly defined DA subtypes of the extended amygdala in zebrafish.

Abstract Image

斑马鱼皮层下多巴胺能神经元属于延伸内侧杏仁核
杏仁核是一个异质性的多核远端脑结构,对脊椎动物的动机和情绪相关行为至关重要。在像硬骨斑马鱼这样的鳍鱼(放线鱼科)中,一种被称为外翻的端脑向外生长过程使得定义杏仁核区域特别具有挑战性。硬骨鱼的特殊之处在于,它们在皮层下发育了大量的多巴胺能(DA)神经元,而在四足动物中,这样的群体不那么突出或只是短暂出现。为了阐明硬骨鱼杏仁核的组织结构,我们采用了一种进化发育的方法,重点研究了pallial下DA神经元的拓扑起源。具体来说,我们分析了酪氨酸羟化酶(Th)的分布,并结合pax6a+b、isl1a、nkx2.1、lhx8a、otpa+b和calb2a的表达模式,作为5日龄和30日龄斑马鱼大脑中不同端脑细分的标志物(Danio rerio, Teleostei)。我们的数据显示,之前确定的腹侧端脑(Vdd)的最背部分需要细分为腹侧pax6a/b阳性部分(Vdd1)和后嗅侧pax6a/b阴性部分(Vdd2)。pax6a阴性的Vdd2部分发育为延伸的内侧杏仁核(EMeA),包括靠近白质-白质下边界的DA群体。我们的研究结果还表明,EMeA DA神经元形成了一个异质的杏仁核神经元群,因为它们表达calb2a和sst7的差异。我们的工作揭示了杏仁核的早期进化和发育,并为斑马鱼扩展杏仁核新定义的DA亚型的功能分析提供了基础。
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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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