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Alpha2-chimaerin interacts with EphA4 and regulates EphA4-dependent growth cone collapse.α2-嵌合蛋白与EphA4相互作用并调节EphA4依赖的生长锥塌陷。
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16347-52. doi: 10.1073/pnas.0706626104. Epub 2007 Oct 2.
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乙酰胆碱影响发育中丘脑轴突的生长锥运动性和形态。

Acetylcholine influences growth cone motility and morphology of developing thalamic axons.

作者信息

Rüdiger Tina, Bolz Jürgen

机构信息

Universität Jena, Institut für Allgemeine Zoologie und Tierphysiologie, Jena, Germany.

出版信息

Cell Adh Migr. 2008 Jan-Mar;2(1):30-7. doi: 10.4161/cam.2.1.5909. Epub 2008 Jan 14.

DOI:10.4161/cam.2.1.5909
PMID:19262162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2635000/
Abstract

The neurotransmitter acetylcholine (ACh) is expressed in the developing telencephalon at the time when thalamic axons project to the cortex, long before synapses are being formed. Since previous studies demonstrated an influence of ACh on neurite extension we used different in vitro assays to examine possible effects of ACh on the growth of thalamic axons. In explant cultures, application of ACh reduced the length of thalamic axons in a dose dependent manner, an effect that could also be evoked by selective muscarinic and nicotinic agonists. Time-lapse imaging of thalamic axons exposed to microscopic gradients of ACh revealed that growth cones no longer advanced, but maintained high filopodial activity. This growth cone pausing was not accompanied by axon retraction or growth cone collapse. It could at least partially be blocked by muscarinic and nicotinic antagonists, indicating that both types of ACh receptors contribute to mediate these effects on thalamic axons. Finally, we also found that ACh changed the morphology of growth cones; they became larger and extended more filopodia. Since such changes in the structure and motility of growth cones are observed at decision regions along the path of many fiber populations including thalamic axons, we suggest that ACh plays a role during the elaboration of thalamocortical projections.

摘要

神经递质乙酰胆碱(ACh)在丘脑轴突投射至皮质时,即在突触形成之前很久,就已在发育中的端脑中表达。由于先前的研究表明ACh对神经突延伸有影响,我们使用了不同的体外试验来检测ACh对丘脑轴突生长的可能作用。在组织块培养中,应用ACh以剂量依赖的方式缩短了丘脑轴突的长度,这种效应也可由选择性毒蕈碱和烟碱激动剂诱发。对暴露于ACh微观梯度下的丘脑轴突进行延时成像显示,生长锥不再前进,但保持着较高的丝状伪足活性。这种生长锥停顿并未伴随轴突回缩或生长锥塌陷。它至少可部分地被毒蕈碱和烟碱拮抗剂阻断,表明这两种类型的ACh受体均参与介导对丘脑轴突的这些作用。最后,我们还发现ACh改变了生长锥的形态;它们变得更大并伸出更多丝状伪足。由于在包括丘脑轴突在内的许多纤维群体路径上的决策区域都观察到了生长锥结构和运动性的这种变化,我们认为ACh在丘脑皮质投射的精细形成过程中发挥作用。