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EphA3 在鸡顶盖中表达,可刺激鼻视网膜神经节细胞轴突生长,并对视网膜顶盖的拓扑图形成是必需的。

EphA3 expressed in the chicken tectum stimulates nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation.

机构信息

Laboratory of Developmental Neurobiology, Institute of Cell Biology and Neurosciences Prof. E. De Robertis (UBA-CONICET), School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.

出版信息

PLoS One. 2012;7(6):e38566. doi: 10.1371/journal.pone.0038566. Epub 2012 Jun 7.

Abstract

BACKGROUND

Retinotopic projection onto the tectum/colliculus constitutes the most studied model of topographic mapping and Eph receptors and their ligands, the ephrins, are the best characterized molecular system involved in this process. Ephrin-As, expressed in an increasing rostro-caudal gradient in the tectum/colliculus, repel temporal retinal ganglion cell (RGC) axons from the caudal tectum and inhibit their branching posterior to their termination zones. However, there are conflicting data regarding the nature of the second force that guides nasal axons to invade and branch only in the caudal tectum/colliculus. The predominant model postulates that this second force is produced by a decreasing rostro-caudal gradient of EphA7 which repels nasal optic fibers and prevents their branching in the rostral tectum/colliculus. However, as optic fibers invade the tectum/colliculus growing throughout this gradient, this model cannot explain how the axons grow throughout this repellent molecule.

METHODOLOGY/PRINCIPAL FINDINGS: By using chicken retinal cultures we showed that EphA3 ectodomain stimulates nasal RGC axon growth in a concentration dependent way. Moreover, we showed that nasal axons choose growing on EphA3-expressing cells and that EphA3 diminishes the density of interstitial filopodia in nasal RGC axons. Accordingly, in vivo EphA3 ectodomain misexpression directs nasal optic fibers toward the caudal tectum preventing their branching in the rostral tectum.

CONCLUSIONS

We demonstrated in vitro and in vivo that EphA3 ectodomain (which is expressed in a decreasing rostro-caudal gradient in the tectum) is necessary for topographic mapping by stimulating the nasal axon growth toward the caudal tectum and inhibiting their branching in the rostral tectum. Furthermore, the ability of EphA3 of stimulating axon growth allows understanding how optic fibers invade the tectum growing throughout this molecular gradient. Therefore, opposing tectal gradients of repellent ephrin-As and of axon growth stimulating EphA3 complement each other to map optic fibers along the rostro-caudal tectal axis.

摘要

背景

视顶盖/丘脑中的视网膜投射构成了最具研究价值的地形映射模型,而 Eph 受体及其配体 Ephrins 是该过程中最具特征性的分子系统。Ephrin-As 在视顶盖/丘脑中呈逐渐增加的前后梯度表达,排斥来自视顶盖尾部的时间性视网膜神经节细胞 (RGC) 轴突,并抑制它们在终止区后的分支。然而,关于引导鼻侧轴突仅在视顶盖/丘脑中入侵和分支的第二种力的性质,存在相互矛盾的数据。主要模型假设,第二种力是由 EphA7 的逐渐增加的前后梯度产生的,该梯度排斥鼻侧视神经纤维并防止它们在视顶盖/丘脑中的分支。然而,由于视神经纤维在整个梯度中侵入视顶盖/丘脑中生长,该模型无法解释轴突如何在整个排斥分子中生长。

方法/主要发现:通过使用鸡视网膜培养物,我们表明 EphA3 外显子在浓度依赖的方式下刺激鼻侧 RGC 轴突生长。此外,我们表明鼻侧轴突选择在 EphA3 表达细胞上生长,并且 EphA3 减少了鼻侧 RGC 轴突中间质丝状伪足的密度。因此,体内 EphA3 外显子异位表达将鼻侧视神经纤维引导向视顶盖尾部,防止它们在视顶盖头部分支。

结论

我们在体外和体内证明 EphA3 外显子(在视顶盖中呈逐渐减少的前后梯度表达)通过刺激鼻侧轴突向视顶盖尾部生长并抑制其在视顶盖头部分支,从而促进地形映射。此外,EphA3 刺激轴突生长的能力允许理解视神经纤维如何在整个分子梯度中侵入视顶盖。因此,排斥 Ephrin-As 的视顶盖梯度和轴突生长刺激 EphA3 的梯度相辅相成,以沿视顶盖前后轴映射视神经纤维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/3369860/dbf43e1b738f/pone.0038566.g001.jpg

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