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Bhlhb5::flpo等位基因揭示了背侧耳蜗核发育对Bhlhb5的需求。

Bhlhb5::flpo allele uncovers a requirement for Bhlhb5 for the development of the dorsal cochlear nucleus.

作者信息

Cai Xiaoyun, Kardon Adam P, Snyder Lindsey M, Kuzirian Marissa S, Minestro Sam, de Souza Luiza, Rubio Maria E, Maricich Stephen M, Ross Sarah E

机构信息

Department of Neurobiology, University of Pittsburgh, 200 Lothrop St., Pittsburgh, PA 15213, USA; The Pittsburgh Center for Pain Research, University of Pittsburgh, 200 Lothrop St., Pittsburgh, PA 15213, USA.

Department of Neurobiology, University of Pittsburgh, 200 Lothrop St., Pittsburgh, PA 15213, USA.

出版信息

Dev Biol. 2016 Jun 15;414(2):149-60. doi: 10.1016/j.ydbio.2016.04.028. Epub 2016 May 3.

Abstract

Auditory information is initially processed in the cochlear nuclei before being relayed to the brain. The cochlear nuclei are subdivided into dorsal, anterior ventral, and posterior ventral domains, each containing several subtypes of neurons that are thought to play discrete roles in the processing of sound. However, the ontogeny of these neurons is poorly understood, and this gap in knowledge hampers efforts to understand the basic neural circuitry of this nucleus. Here, we reveal that Bhlhb5 is expressed in both excitatory (unipolar brush cells) and inhibitory neurons (cartwheel cells) of the DCN during development. To gain genetic access to Bhlhb5-expressing neurons in the DCN, we generated a Bhlhb5::flpo knockin allele. Using an intersectional genetic strategy, we labeled cartwheel cells, thereby providing proof of concept that subpopulations of Bhlhb5-expressing neurons can be genetically targeted. Moreover, fate-mapping experiments using this allele revealed that Bhlhb5 is required for the proper development of the DCN, since mice lacking Bhlhb5 showed a dramatically diminished number of neurons, including unipolar brush and cartwheel cells. Intriguingly, the Bhlhb5::flpo allele also genetically labels numerous other regions of the nervous system that process sensory input, including the dorsal horn, the retina, and the nucleus of the lateral olfactory tract, hinting at a more general role for Bhlhb5 in the development of neurons that mediate sensory integration.

摘要

听觉信息最初在耳蜗核中进行处理,然后再传递到大脑。耳蜗核可细分为背侧、前腹侧和后腹侧区域,每个区域都包含几种神经元亚型,这些神经元被认为在声音处理中发挥着不同的作用。然而,这些神经元的个体发生过程却知之甚少,这一知识空白阻碍了我们对该核基本神经回路的理解。在这里,我们发现Bhlhb5在发育过程中在背侧耳蜗核的兴奋性(单极刷状细胞)和抑制性神经元(车轮状细胞)中均有表达。为了通过遗传学方法研究背侧耳蜗核中表达Bhlhb5的神经元,我们构建了一个Bhlhb5::flpo敲入等位基因。利用一种交叉遗传策略,我们标记了车轮状细胞,从而证明了表达Bhlhb5的神经元亚群可以通过遗传学方法进行靶向研究。此外,使用该等位基因进行的命运图谱实验表明,Bhlhb5是背侧耳蜗核正常发育所必需的,因为缺乏Bhlhb5的小鼠中神经元数量显著减少,包括单极刷状细胞和车轮状细胞。有趣的是,Bhlhb5::flpo等位基因还通过遗传学方法标记了神经系统中许多其他处理感觉输入的区域,包括背角、视网膜和外侧嗅束核,这表明Bhlhb5在介导感觉整合的神经元发育中可能具有更广泛的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5fa/4930277/6b6b45f4e77b/nihms795579f1.jpg

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