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弥合突触前毛细胞功能与神经声音编码之间的差距。

Bridging the gap between presynaptic hair cell function and neural sound encoding.

作者信息

Jaime Tobón Lina María, Moser Tobias

机构信息

Auditory Neuroscience and Synaptic Nanophysiology Group, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Institute for Auditory Neuroscience, University Medical Center Göttingen, Göttingen, Germany.

出版信息

Elife. 2024 Dec 24;12:RP93749. doi: 10.7554/eLife.93749.

DOI:10.7554/eLife.93749
PMID:39718472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11668530/
Abstract

Neural diversity can expand the encoding capacity of a circuitry. A striking example of diverse structure and function is presented by the afferent synapses between inner hair cells (IHCs) and spiral ganglion neurons (SGNs) in the cochlea. Presynaptic active zones at the pillar IHC side activate at lower IHC potentials than those of the modiolar side that have more presynaptic Ca channels. The postsynaptic SGNs differ in their spontaneous firing rates, sound thresholds, and operating ranges. While a causal relationship between synaptic heterogeneity and neural response diversity seems likely, experimental evidence linking synaptic and SGN physiology has remained difficult to obtain. Here, we aimed at bridging this gap by ex vivo paired recordings of murine IHCs and postsynaptic SGN boutons with stimuli and conditions aimed to mimic those of in vivo SGN characterization. Synapses with high spontaneous rate of release () were found predominantly on the pillar side of the IHC. These high synapses had larger and more temporally compact spontaneous EPSCs, lower voltage thresholds, tighter coupling of Ca channels and vesicular release sites, shorter response latencies, and higher initial release rates. This study indicates that synaptic heterogeneity in IHCs directly contributes to the diversity of spontaneous and sound-evoked firing of SGNs.

摘要

神经多样性可以扩展神经回路的编码能力。耳蜗内毛细胞(IHC)与螺旋神经节神经元(SGN)之间的传入突触展现出了结构和功能多样性的一个显著例子。在IHC柱状侧的突触前活动区在比具有更多突触前钙通道的蜗轴侧更低的IHC电位时被激活。突触后SGN在其自发放电率、声音阈值和工作范围方面存在差异。虽然突触异质性与神经反应多样性之间似乎可能存在因果关系,但将突触生理学与SGN生理学联系起来的实验证据仍然难以获得。在这里,我们旨在通过对小鼠IHC和突触后SGN终扣进行离体配对记录,并采用旨在模拟体内SGN特征的刺激和条件来填补这一空白。发现具有高自发释放率()的突触主要位于IHC的柱状侧。这些高 突触具有更大且在时间上更紧凑的自发兴奋性突触后电流(sEPSC)、更低的电压阈值、钙通道与囊泡释放位点的更紧密耦合、更短的反应潜伏期以及更高的初始释放率。这项研究表明,IHC中的突触异质性直接促成了SGN自发放电和声音诱发放电的多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/e0fbc143d080/elife-93749-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/404091b39f6d/elife-93749-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/c78db6011f1e/elife-93749-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/769d1c8397e2/elife-93749-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/a0e65826045c/elife-93749-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/379abbe840da/elife-93749-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/bc09097d0214/elife-93749-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/c8b1d1d24763/elife-93749-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/6290c0f8280c/elife-93749-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/e0fbc143d080/elife-93749-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/404091b39f6d/elife-93749-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/c78db6011f1e/elife-93749-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/769d1c8397e2/elife-93749-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/a0e65826045c/elife-93749-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/379abbe840da/elife-93749-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/bc09097d0214/elife-93749-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/c8b1d1d24763/elife-93749-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/6290c0f8280c/elife-93749-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b370/11668530/e0fbc143d080/elife-93749-fig4-figsupp1.jpg

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Molecular signatures define subtypes of auditory afferents with distinct peripheral projection patterns and physiological properties.
分子特征定义了具有不同外周投射模式和生理特性的听觉传入神经亚型。
Proc Natl Acad Sci U S A. 2023 Aug;120(31):e2217033120. doi: 10.1073/pnas.2217033120. Epub 2023 Jul 24.
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Optogenetics and electron tomography for structure-function analysis of cochlear ribbon synapses.光遗传学和电子断层扫描技术在耳蜗带状突触结构功能分析中的应用。
Elife. 2022 Dec 23;11:e79494. doi: 10.7554/eLife.79494.
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The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses.SNARE蛋白SNAP-25是听觉毛细胞带状突触正常胞吐作用所必需的。
iScience. 2022 Nov 22;25(12):105628. doi: 10.1016/j.isci.2022.105628. eCollection 2022 Dec 22.
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