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<p>The CUGBP Elav-like family 4 (CELF4), an RNA-binding protein, is dynamically expressed in spiral ganglion neurons (SGNs) in the cochlea over development, but how <i>Celf4</i> is involved in regulating hearing functions is poorly understood. In this study, we generated a <i>Celf4</i><sup>±</sup> mouse line and examined changes in the first two synapses along the auditory pathways. Firstly, we found that hearing functions were largely intact in <i>Celf4</i><sup>±</sup> mice, with exception of reduced amplitude for Wave II of auditory brainstem responses (ABRs) and increased delays for Wave II and IV, both in case of 4&#xa0;kHz only. Secondly, we found that counts of inner and outer hair cells (IHCs and OHCs) and SGNs remained unchanged in <i>Celf4</i><sup>±</sup> mice, and that the number and function of ribbon synapses between IHCs and SGNs were comparable between WT and <i>Celf4</i><sup>±</sup> mice. Lastly, function of the endbulb of Held synapse, formed between auditory nerve fibers (ANFs) of SGNs and bushy cells in the cochlear nucleus, was significantly altered in <i>Celf4</i><sup>±</sup> mice. Specifically, synaptic vesicle release was subtly reduced, and excitability of bushy cells was significantly dampened, likely due to a hyperpolarized resting membrane potential. Furthermore, we found that spike kinetics was significantly faster in <i>Celf4</i><sup>±</sup> bushy cells, likely caused by a larger fast-inactivating A-type potassium current (I<sub>A</sub>) found in these cells. In conclusion, we found that <i>Celf4</i> haploinsufficiency altered transmission at the endbulb of Held synapses in the cochlear nucleus in a significant and multifaceted manner, revealing the roles of <i>Celf4</i> in regulating hearing functions.</p> Graphical Abstract <p>Title: Schematic representation of the experimental approach and major findings.</p> <p>Legend: In mice with <i>Celf4</i> haploinsufficiency, we found that while function at hair cell ribbon synapses was largely preserved, transmission at the endbulb of Held synapse was significantly altered, including subtly reduced release of synaptic vesicles from the endbulb, dampened excitability in bushy cells, and accelerated spike kinetics caused by enhanced voltage-gated K<sup>+</sup> current.</p> <p></p>

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Celf4 Regulates Excitability of Bushy Cells in the Cochlear Nucleus of the Mouse Brainstem

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月24日

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  • Yige Li,
  • Siyu Qiu,
  • Fang Wang,
  • Zhenghong Bi,
  • Zhiyong Liu,
  • Yingzi He,
  • Geng-Lin Li

摘要

The CUGBP Elav-like family 4 (CELF4), an RNA-binding protein, is dynamically expressed in spiral ganglion neurons (SGNs) in the cochlea over development, but how Celf4 is involved in regulating hearing functions is poorly understood. In this study, we generated a Celf4± mouse line and examined changes in the first two synapses along the auditory pathways. Firstly, we found that hearing functions were largely intact in Celf4± mice, with exception of reduced amplitude for Wave II of auditory brainstem responses (ABRs) and increased delays for Wave II and IV, both in case of 4 kHz only. Secondly, we found that counts of inner and outer hair cells (IHCs and OHCs) and SGNs remained unchanged in Celf4± mice, and that the number and function of ribbon synapses between IHCs and SGNs were comparable between WT and Celf4± mice. Lastly, function of the endbulb of Held synapse, formed between auditory nerve fibers (ANFs) of SGNs and bushy cells in the cochlear nucleus, was significantly altered in Celf4± mice. Specifically, synaptic vesicle release was subtly reduced, and excitability of bushy cells was significantly dampened, likely due to a hyperpolarized resting membrane potential. Furthermore, we found that spike kinetics was significantly faster in Celf4± bushy cells, likely caused by a larger fast-inactivating A-type potassium current (IA) found in these cells. In conclusion, we found that Celf4 haploinsufficiency altered transmission at the endbulb of Held synapses in the cochlear nucleus in a significant and multifaceted manner, revealing the roles of Celf4 in regulating hearing functions.

Graphical Abstract

Title: Schematic representation of the experimental approach and major findings.

Legend: In mice with Celf4 haploinsufficiency, we found that while function at hair cell ribbon synapses was largely preserved, transmission at the endbulb of Held synapse was significantly altered, including subtly reduced release of synaptic vesicles from the endbulb, dampened excitability in bushy cells, and accelerated spike kinetics caused by enhanced voltage-gated K+ current.