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本文引用的文献

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Maturation of synaptic partners: functional phenotype and synaptic organization tuned in synchrony.突触伙伴的成熟:功能表型和突触组织的同步调节。
J Physiol. 2010 Nov 15;588(Pt 22):4365-85. doi: 10.1113/jphysiol.2010.198564. Epub 2010 Sep 20.
2
Ephrin-B reverse signaling is required for formation of strictly contralateral auditory brainstem pathways.Ephrin-B 反向信号对于严格对侧听觉脑干通路的形成是必需的。
J Neurosci. 2010 Jul 21;30(29):9840-9. doi: 10.1523/JNEUROSCI.0386-10.2010.
3
Septins regulate developmental switching from microdomain to nanodomain coupling of Ca(2+) influx to neurotransmitter release at a central synapse.Septins 调节中央突触中从 Ca(2+)流入到神经递质释放的微域偶联到纳域偶联的发育转换。
Neuron. 2010 Jul 15;67(1):100-15. doi: 10.1016/j.neuron.2010.06.003.
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Localization of Kv1.3 channels in presynaptic terminals of brainstem auditory neurons.Kv1.3 通道在脑干听觉神经元突触前末梢的定位。
J Comp Neurol. 2010 Aug 15;518(16):3205-20. doi: 10.1002/cne.22393.
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Developmental shift to a mechanism of synaptic vesicle endocytosis requiring nanodomain Ca2+.发育过程中向需要纳米域 Ca2+的突触小泡内吞作用机制的转变。
Nat Neurosci. 2010 Jul;13(7):838-44. doi: 10.1038/nn.2576. Epub 2010 Jun 20.
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Going native: voltage-gated potassium channels controlling neuronal excitability.归巢:电压门控钾通道调节神经元兴奋性。
J Physiol. 2010 Sep 1;588(Pt 17):3187-200. doi: 10.1113/jphysiol.2010.191973. Epub 2010 Jun 2.
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Neuron-astrocyte interactions in the medial nucleus of the trapezoid body.梯形体内侧核对神经元-星形细胞相互作用的影响。
J Gen Physiol. 2010 Jun;135(6):583-94. doi: 10.1085/jgp.200910354. Epub 2010 May 17.
8
Developmental expression of Synaptotagmin isoforms in single calyx of Held-generating neurons.单一 Held 神经元中突触结合蛋白同型异构体的发育表达。
Mol Cell Neurosci. 2010 Aug;44(4):374-85. doi: 10.1016/j.mcn.2010.05.002. Epub 2010 May 12.
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Genetic dissection of the function of hindbrain axonal commissures.对后脑轴突连合功能的遗传剖析。
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10
Regulation of Kv channel expression and neuronal excitability in rat medial nucleus of the trapezoid body maintained in organotypic culture.在器官型培养中维持的大鼠梯形束中间核中 Kv 通道表达和神经元兴奋性的调节。
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Held 氏小囊的形成和成熟。

Formation and maturation of the calyx of Held.

机构信息

Department of Neurobiology and Behavior, University of California, Irvine, 2205 McGaugh Hall, Irvine, CA 92697-4550, USA.

出版信息

Hear Res. 2011 Jun;276(1-2):70-8. doi: 10.1016/j.heares.2010.11.004. Epub 2010 Nov 18.

DOI:10.1016/j.heares.2010.11.004
PMID:21093567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3109188/
Abstract

Sound localization requires precise and specialized neural circuitry. A prominent and well-studied specialization is found in the mammalian auditory brainstem. Globular bushy cells of the ventral cochlear nucleus (VCN) project contralaterally to neurons of the medial nucleus of the trapezoid body (MNTB), where their large axons terminate on cell bodies of MNTB principal neurons, forming the calyces of Held. The VCN-MNTB pathway is necessary for the accurate computation of interaural intensity and time differences; MNTB neurons provide inhibitory input to the lateral superior olive, which compares levels of excitation from the ipsilateral ear to levels of tonotopically matched inhibition from the contralateral ear, and to the medial superior olive, where precise inhibition from MNTB neurons tunes the delays of binaural excitation. Here we review the morphological and physiological aspects of the development of the VCN-MNTB pathway and its calyceal termination, along with potential mechanisms that give rise to its precision. During embryonic development, VCN axons grow towards the midline, cross the midline into the region of the presumptive MNTB and then form collateral branches that will terminate in calyces of Held. In rodents, immature calyces of Held appear in MNTB during the first few days of postnatal life. These calyces mature morphologically and physiologically over the next three postnatal weeks, enabling fast, high fidelity transmission in the VCN-MNTB pathway.

摘要

声音定位需要精确和专门的神经回路。哺乳动物听觉脑干中存在一种突出且研究充分的专门化现象。腹侧耳蜗核 (VCN) 的球状布什细胞向梯形体中间核 (MNTB) 的神经元对侧投射,其大轴突终止于 MNTB 主神经元的胞体上,形成赫尔德杯。VCN-MNTB 通路是准确计算两耳强度和时间差异所必需的;MNTB 神经元向外侧上橄榄核提供抑制性输入,该核比较同侧耳的兴奋水平与对侧耳的音调匹配抑制水平,并向内侧上橄榄核提供精确的抑制性输入,从而调节双耳兴奋的延迟。在这里,我们回顾了 VCN-MNTB 通路及其赫尔德杯终止的形态和生理发育方面,以及产生其精确性的潜在机制。在胚胎发育过程中,VCN 轴突向中线生长,穿过中线进入假定的 MNTB 区域,然后形成将在赫尔德杯终止的侧支。在啮齿动物中,未成熟的赫尔德杯在出生后的头几天出现在 MNTB 中。这些赫尔德杯在出生后的前三个星期内在形态和生理上成熟,从而使 VCN-MNTB 通路能够快速、高保真地传输。