原粘连蛋白19调节发育中的章鱼视网膜通路的轴突导向。

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Jane Jung, Jugeon Park, Sihyeon Park, Chul Hoon Kim, Hosung Jung
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引用次数: 0

摘要

原粘连蛋白19(Pcdh19)是一种嗜同性细胞粘附分子,参与多种神经元功能。在这里,我们利用发育中的爪蟾视网膜系统检测了 Pcdh19 是否在轴突导向中起调控作用。我们对翻译阻断反义吗啉寡核苷酸进行了靶向显微注射,以选择性地敲除 Pcdh19 在中枢神经系统中的表达。敲除Pcdh19会导致视网膜神经节细胞(RGC)轴突导航错误,特别是在视交叉。在Pcdh19被敲除的胚胎中,RGC轴突不是投射到对侧视神经乳头,而是错误地投射到同侧。虽然这些轴突错误地投射到了同侧大脑半球,但却正确地到达了视神经乳头。这些数据表明,Pcdh19在防止源自对侧眼睛的RGC轴突在视交叉混合方面起着关键作用,突出了细胞粘附在RGC轴突捆绑中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocadherin 19 regulates axon guidance in the developing Xenopus retinotectal pathway.

Protocadherin 19 (Pcdh19) is a homophilic cell adhesion molecule and is involved in a variety of neuronal functions. Here, we tested whether Pcdh19 has a regulatory role in axon guidance using the developing Xenopus retinotectal system. We performed targeted microinjections of a translation blocking antisense morpholino oligonucleotide to knock down the expression of Pcdh19 selectively in the central nervous system. Knocking down Pcdh19 expression resulted in navigational errors of retinal ganglion cell (RGC) axons specifically at the optic chiasm. Instead of projecting to the contralateral optic tectum, RGC axons in the Pcdh19-depleted embryo misprojected ipsilaterally. Although incorrectly delivered into the ipsilateral brain hemisphere, these axons correctly reached the optic tectum. These data suggest that Pcdh19 has a critical role in preventing mixing of RGC axons originating from the opposite eyes at the optic chiasm, highlighting the importance of cell adhesion in bundling of RGC axons.

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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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