首页> 外文期刊>The European Journal of Neuroscience >Membrane-associated guidance cues direct the innervation of forebrain and midbrain by dorsal raphe-derived serotonergic axons.
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Membrane-associated guidance cues direct the innervation of forebrain and midbrain by dorsal raphe-derived serotonergic axons.

机译:膜相关的引导线索通过背侧网纹来源的5-羟色胺能神经轴突指导前脑和中脑的神经支配。

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Abstract Unlike many neurons that extend an axon precisely to a single target, individual dorsal raphe 5-HT neurons project to multiple brain regions and their axon terminals often lack classical synaptic specializations. It is not known how 5-HT axon collaterals select between multiple target fields, or even if 5-HT axons require specific guidance cues to innervate their targets. Nor is it known how these axon collaterals are restrained within specific innervation target regions. To investigate this, we challenged explants of dorsal raphe with co-explants, or cell membrane preparations of ventral midbrain, striatum or cerebral cortex. We provide evidence for membrane-associated cues that promote 5-HT axon growth into each of these three target regions. The axon growth-promoting activity was heat-, protease- and phosphatidylinositol-phospholipase-C (PI-PLC)-sensitive. Interestingly, 5-HT axons specifically lost the ability to grow in heterotypic explants, or membrane carpets, following contact with ventral midbrain or striatal, but not cortical, explants or membranes. This inductive activity associated with striatal and ventral midbrain membranes was sensitive to both high salt extraction and PI-PLC treatment. By contrast, the activity that inhibited 5-HT axon growth onto heterotypic membranes was sensitive only to high salt extraction. These results provide evidence that a glycosylphosphatidylinositol (GPI)-linked membrane protein promotes 5-HT axon growth, and that short-range membrane-bound, as well as GPI-linked, molecules contribute to the guidance of 5-HT axon collaterals. These findings suggest that 5-HT axon collaterals acquire a target-induced growth-inhibitory response to alternative targets, increasing their selectivity for the newly innervated field.
机译:摘要与许多将轴突精确地延伸到单个靶标的神经元不同,单个背脊5-HT神经元投射到多个大脑区域,它们的轴突末端通常缺乏经典的突触专长。尚不知道5-HT轴突抵押品如何在多个目标区域之间进行选择,或者甚至5-HT轴突需要特定的指导线索来支配其目标。还不知道如何将这些轴突侧支限制在特定的神经支配目标区域内。为了对此进行研究,我们用同种外植体或腹侧中脑,纹状体或大脑皮层的细胞膜制剂挑战了背缝的外植体。我们为促进5-HT轴突生长进入这三个目标区域的每个膜相关的提示提供证据。轴突生长促进活性是热,蛋白酶和磷脂酰肌醇磷脂酶-C(PI-PLC)敏感的。有趣的是,5-HT轴突在与腹中脑或纹状体(而非皮质,外植体或膜)接触后,特别失去了在异型外植体或膜毯中生长的能力。与纹状体和腹中脑膜相关的这种诱导活性对高盐提取和PI-PLC处理均敏感。相比之下,抑制5-HT轴突生长到异型膜上的活性仅对高盐提取敏感。这些结果提供了糖基磷脂酰肌醇(GPI)连接的膜蛋白促进5-HT轴突生长的证据,而短程膜结合的以及GPI连接的分子也有助于5-HT轴突侧支的引导。这些发现表明5-HT轴突抵押品获得了目标诱导的对其他目标的抑制生长反应,从而增加了它们对新神经支配领域的选择性。

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