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非靶点依赖性ephrina/EphA介导的轴突-轴突排斥作为视网膜-丘脑映射中的一个新因素。

Target-independent ephrina/EphA-mediated axon-axon repulsion as a novel element in retinocollicular mapping.

作者信息

Suetterlin Philipp, Drescher Uwe

机构信息

MRC Centre for Developmental Neurobiology, New Hunt's House, Guy's Campus, Kings College London, London SE1 1UL, UK.

MRC Centre for Developmental Neurobiology, New Hunt's House, Guy's Campus, Kings College London, London SE1 1UL, UK.

出版信息

Neuron. 2014 Nov 19;84(4):740-52. doi: 10.1016/j.neuron.2014.09.023. Epub 2014 Oct 23.

DOI:10.1016/j.neuron.2014.09.023
PMID:25451192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4250266/
Abstract

EphrinAs and EphAs play critical roles during topographic map formation in the retinocollicular projection; however, their complex expression patterns in both the retina and superior colliculus (SC) have made it difficult to uncover their precise mechanisms of action. We demonstrate here that growth cones of temporal axons collapse when contacting nasal axons in vitro, and removing ephrinAs from axonal membranes by PI-PLC treatment abolishes this response. In conditional knockout mice, temporal axons display no major targeting defects when ephrinA5 is removed only from the SC, but substantial mapping defects were observed when ephrinA5 expression was removed from both the SC and from the retina, with temporal axons invading the target areas of nasal axons. Together, these data indicate that ephrinA5 drives repellent interactions between temporal and nasal axons within the SC, and demonstrates for the first time that target-independent mechanisms play an essential role in retinocollicular map formation in vivo.

摘要

EphrinA家族和EphA家族在视网膜-丘脑投射的拓扑图形成过程中发挥着关键作用;然而,它们在视网膜和上丘(SC)中复杂的表达模式使得难以揭示其精确的作用机制。我们在此证明,在体外,颞侧轴突的生长锥在与鼻侧轴突接触时会发生塌陷,而通过磷脂酰肌醇特异性磷脂酶C(PI-PLC)处理从轴突膜上去除ephrinA家族蛋白可消除这种反应。在条件性基因敲除小鼠中,仅从SC中去除ephrinA5时,颞侧轴突未显示出主要的靶向缺陷,但当从SC和视网膜中都去除ephrinA5表达时,观察到明显的图谱缺陷,颞侧轴突侵入鼻侧轴突的靶区。这些数据共同表明,ephrinA5驱动了SC内颞侧和鼻侧轴突之间的排斥性相互作用,并首次证明了与靶标无关的机制在体内视网膜-丘脑图谱形成中起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/155fc8a3776e/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/1575e8d6377e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/edc6e8240ca5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/0eecf9188ce3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/4fa38e4fca2f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/619d3e777007/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/757d88717c97/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/155fc8a3776e/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/1575e8d6377e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/edc6e8240ca5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/0eecf9188ce3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/4fa38e4fca2f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/619d3e777007/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/757d88717c97/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c784/4250266/155fc8a3776e/gr7.jpg

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