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胚胎外胚层发育蛋白1对于外侧丘系腹侧核中神经元的存活是必需的。

En1 is necessary for survival of neurons in the ventral nuclei of the lateral lemniscus.

作者信息

Altieri Stefanie C, Zhao Tianna, Jalabi Walid, Romito-DiGiacomo Rita R, Maricich Stephen M

机构信息

Richard King Mellon Institute for Pediatric Research, Department of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania, 15224.

Department of Pediatrics, Case Western Reserve University, Cleveland, Ohio, 44106.

出版信息

Dev Neurobiol. 2016 Nov;76(11):1266-1274. doi: 10.1002/dneu.22388. Epub 2016 Apr 5.

Abstract

The ventral nuclei of the lateral lemniscus (VNLL) are part of the central auditory system thought to participate in temporal sound processing. While the timing and location of VNLL neurogenesis have been determined, the genetic factors that regulate VNLL neuron development are unknown. Here, we use genetic fate-mapping techniques to demonstrate that all glycinergic and glycinergic/GABAergic VNLL neurons derive from a cellular lineage that expresses the homeobox transcription factor Engrailed 1 (En1). We also show that En1 deletion does not affect migration or adoption of a neuronal cell fate but does lead to VNLL neuron death during development. Furthermore, En1 deletion blocks expression of the transcription factor FoxP1 in a subset of VNLL neurons. Together, these data identify En1 as a gene important for VNLL neuron development and survival. © 2016 Wiley Periodicals, Inc. Develop Neurobiol 76: 1266-1274, 2016.

摘要

外侧丘系腹侧核(VNLL)是中枢听觉系统的一部分,被认为参与时间性声音处理。虽然已经确定了VNLL神经发生的时间和位置,但调节VNLL神经元发育的遗传因素尚不清楚。在这里,我们使用遗传命运映射技术来证明,所有甘氨酸能和甘氨酸能/γ-氨基丁酸能VNLL神经元都源自表达同源框转录因子Engrailed 1(En1)的细胞谱系。我们还表明,En1缺失不影响神经元细胞命运的迁移或采用,但确实会导致发育过程中VNLL神经元死亡。此外,En1缺失会阻断VNLL神经元亚群中转录因子FoxP1的表达。总之,这些数据确定En1是对VNLL神经元发育和存活很重要的基因。©2016威利期刊公司。《发育神经生物学》76: 1266 - 1274, 2016。

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本文引用的文献

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En1 directs superior olivary complex neuron positioning, survival, and expression of FoxP1.
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