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Sonic hedgehog 通过糖蛋白 1 依赖的方式调节其自身在后交叉连合轴突上的受体。

Sonic hedgehog regulates its own receptor on postcrossing commissural axons in a glypican1-dependent manner.

机构信息

Institute of Molecular Life Sciences, Neuroscience Center Zurich, University of Zurich, CH-8057 Zurich, Switzerland.

出版信息

Neuron. 2013 Aug 7;79(3):478-91. doi: 10.1016/j.neuron.2013.05.025.

Abstract

Upon reaching their intermediate target, the floorplate, commissural axons acquire responsiveness to repulsive guidance cues, allowing the axons to exit the midline and adopt a contralateral, longitudinal trajectory. The molecular mechanisms that regulate this switch from attraction to repulsion remain poorly defined. Here, we show that the heparan sulfate proteoglycan Glypican1 (GPC1) is required as a coreceptor for the Shh-dependent induction of Hedgehog-interacting protein (Hhip) in commissural neurons. In turn, Hhip is required for postcrossing axons to respond to a repulsive anteroposterior Shh gradient. Thus, Shh is a cue with dual function. In precrossing axons it acts as an attractive guidance molecule in a transcription-independent manner. At the same time, Shh binds to GPC1 to induce the expression of its own receptor, Hhip, which mediates the repulsive response of postcrossing axons to Shh. Our study characterizes a molecular mechanism by which navigating axons switch their responsiveness at intermediate targets.

摘要

当到达它们的中间目标——基板时,连合轴突获得了对排斥性导向线索的反应能力,从而使轴突离开中线并采用对侧的纵向轨迹。调节这种从吸引到排斥转变的分子机制仍未得到很好的定义。在这里,我们表明硫酸乙酰肝素蛋白聚糖 1 (GPC1) 作为 Shh 依赖性诱导连合神经元 Hedgehog-interacting protein (Hhip) 的核心受体是必需的。反过来,Hhip 对于后交叉轴突对排斥性前后 Shh 梯度的反应是必需的。因此,Shh 是一种具有双重功能的线索。在交叉前轴突中,它以非转录依赖的方式充当有吸引力的导向分子。同时,Shh 与 GPC1 结合,诱导其自身受体 Hhip 的表达,Hhip 介导后交叉轴突对 Shh 的排斥反应。我们的研究描述了一种分子机制,通过该机制,导航轴突在中间目标处切换其反应性。

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