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表皮生长因子受体的激活介导了烟草天蛾发育中的嗅觉系统中受体轴突的分选和延伸。

Activation of epidermal growth factor receptor mediates receptor axon sorting and extension in the developing olfactory system of the moth Manduca sexta.

作者信息

Gibson Nicholas J, Tolbert Leslie P

机构信息

Arizona Research Laboratories Division of Neurobiology, University of Arizona, Tucson, Arizona 85721, USA.

出版信息

J Comp Neurol. 2006 Apr 10;495(5):554-72. doi: 10.1002/cne.20890.

Abstract

During development of the adult olfactory system of the moth Manduca sexta, olfactory receptor neurons extend axons from the olfactory epithelium in the antenna into the brain. As they arrive at the brain, interactions with centrally derived glial cells cause axons to sort and fasciculate with other axons destined to innervate the same glomeruli. Here we report studies indicating that activation of the epidermal growth factor receptor (EGFR) is involved in axon ingrowth and targeting. Blocking the EGFR kinase domain pharmacologically leads to stalling of many axons in the sorting zone and nerve layer as well as abnormal axonal fasciculation in the sorting zone. We also find that neuroglian, an IgCAM known to activate the EGFR through homophilic interactions in other systems, is transiently present on olfactory receptor neuron axons and on glia during the critical stages of the sorting process. The neuroglian is resistant to extraction with Triton X-100 in the sorting zone and nerve layer, possibly indicating its stabilization by homophilic binding in these regions. Our results suggest a mechanism whereby neuroglian molecules on axons and possibly sorting zone glia bind homophilically, leading to activation of EGFRs, with subsequent effects on axon sorting, pathfinding, and extension, and glomerulus development.

摘要

在烟草天蛾成虫嗅觉系统的发育过程中,嗅觉受体神经元将轴突从触角中的嗅觉上皮延伸至大脑。当它们抵达大脑时,与源自中枢的神经胶质细胞的相互作用会使轴突与其他注定要支配相同神经小球的轴突进行分类和成束。在此,我们报告的研究表明,表皮生长因子受体(EGFR)的激活参与轴突向内生长和靶向。药理学上阻断EGFR激酶结构域会导致许多轴突在分类区和神经层停滞,以及分类区轴突异常成束。我们还发现,神经胶质粘连蛋白(neuroglian)是一种已知在其他系统中通过同源相互作用激活EGFR的免疫球蛋白超家族细胞粘附分子(IgCAM),在分类过程的关键阶段,它短暂地存在于嗅觉受体神经元轴突和神经胶质细胞上。在分类区和神经层,神经胶质粘连蛋白对Triton X-100提取具有抗性,这可能表明它在这些区域通过同源结合而稳定。我们的结果提示了一种机制,即轴突上的神经胶质粘连蛋白分子以及可能的分类区神经胶质细胞通过同源结合,导致EGFR激活,随后影响轴突分类、寻路和延伸,以及神经小球发育。

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