Inactivity of Stat3 in sensory and non-sensory cells of the mature cochlea.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Frontiers in Molecular Neuroscience Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.3389/fnmol.2024.1455136
L Bieniussa, C Stolte, P Arampatzi, J Engert, J Völker, R Hagen, S Hackenberg, K Rak
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Abstract

Signal transducer and activator of transcription 3 (Stat3) plays a role in various cellular processes such as differentiation, inflammation, cell survival and microtubule dynamics, depending on the cell type and the activated signaling pathway. Stat3 is highly expressed in the hair cells and supporting cells of the cochlea and is essential for the differentiation of mouse hair cells in the early embryonic stage. However, it is unclear how Stat3 contributes to the correct function of cells in the organ of Corti postnatally. To investigate this, an inducible Cre/loxp system was used to knock out Stat3 in either the outer hair cells or the supporting cells. The results showed that the absence of Stat3 in either the outer hair cells or the supporting cells resulted in hearing loss without altering the morphology of the organ of Corti. Molecular analysis of the outer hair cells revealed an inflammatory process with increased cytokine production and upregulation of the NF-kB pathway. However, the absence of Stat3 in the supporting cells resulted in reduced microtubule stability. In conclusion, Stat3 is a critical protein for the sensory epithelium of the cochlea and hearing and functions in a cell and function-specific manner.

成熟耳蜗感官细胞和非感官细胞中 Stat3 的非活性。
信号转导和转录激活因子 3(Stat3)在分化、炎症、细胞存活和微管动力学等多种细胞过程中发挥作用,这取决于细胞类型和激活的信号通路。Stat3 在耳蜗的毛细胞和支持细胞中高度表达,并且在胚胎早期阶段对小鼠毛细胞的分化至关重要。然而,目前还不清楚 Stat3 如何促进出生后耳蜗器官细胞的正确功能。为了研究这个问题,我们利用诱导性 Cre/loxp 系统敲除了外毛细胞或支持细胞中的 Stat3。结果显示,外毛细胞或支持细胞中的Stat3缺失会导致听力损失,但不会改变Corti器官的形态。对外毛细胞的分子分析表明,炎症过程中细胞因子分泌增加,NF-kB通路上调。然而,支持细胞中缺乏 Stat3 会导致微管稳定性降低。总之,Stat3 是耳蜗感觉上皮细胞和听力的关键蛋白,以细胞和功能特异性的方式发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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