Kolliker's Organ and Its Functional Role in the Development of Corti's Organ and Auditory Systems.

IF 1.8 Q1 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY
Valeria Caragli, Valerio M Di Pasquale Fiasca, Elisabetta Genovese, Alessandro Martini
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Abstract

Background: Kölliker's organ (KO), a transient structure in the cochlea, plays a critical role in the auditory maturation of mammals, particularly during embryonic and early postnatal development. This organ is essential for the proper differentiation and function of cochlear cells, acting as a pivotal source of signalling molecules that influence hair cell development and synaptic connectivity. Methods: This study systematically analyses the literature according to the PRISMA statement in order to evaluate the function roles of KO during cochlea development, reporting the molecular mechanisms and signalling pathways involved. Results: From our study, it emerged that KO supporting cells release adenosine triphosphate (ATP) through connexin hemichannels, initiating a cascade of intracellular calcium (Ca2+) signalling in adjacent inner hair cells (IHCs). This signalling promotes the release of glutamate, facilitating synaptic excitation of afferent nerve fibres and enhancing auditory neuron maturation prior to the onset of hearing. Additionally, the spontaneous electrical activity generated within KO supports the establishment of essential neural connections in the auditory pathway. The dynamic interplay between ATP release, Ca2+ signalling, and morphological changes in KO is crucial for cochlear compartmentalisation and fluid regulation, contributing to the formation of endolymph and perilymph. Furthermore, KO supports cellular plasticity and may provide a reservoir of precursor cells capable of trans-differentiating into hair cells under specific conditions. Conclusions: Dysregulation of KO function or delayed degeneration of its supporting cells has been implicated in auditory disorders, underscoring the importance of this organ in normal cochlear development and auditory function. Despite its identification over a century ago, further investigation is necessary to elucidate the molecular mechanisms underlying KO's contributions to auditory maturation, particularly in human physiology.

Abstract Image

Abstract Image

科利克氏器官及其在科利克氏器官和听觉系统发育中的功能作用。
背景:Kölliker的器官(KO)是耳蜗中的一种瞬态结构,在哺乳动物的听觉成熟中起着关键作用,特别是在胚胎和出生后早期发育过程中。这个器官对耳蜗细胞的正常分化和功能至关重要,是影响毛细胞发育和突触连通性的信号分子的关键来源。方法:本研究根据PRISMA声明系统分析文献,评价KO在耳蜗发育过程中的功能作用,报道其分子机制和信号通路。结果:从我们的研究中,我们发现KO支持细胞通过连接蛋白半通道释放三磷酸腺苷(ATP),在邻近的内毛细胞(IHCs)中启动细胞内钙(Ca2+)信号传导的级联。这种信号促进谷氨酸的释放,促进传入神经纤维的突触兴奋,并在听力发生之前促进听觉神经元的成熟。此外,KO内产生的自发电活动支持听觉通路中基本神经连接的建立。在KO中,ATP释放、Ca2+信号和形态学变化之间的动态相互作用对于耳蜗区隔化和液体调节至关重要,有助于形成内淋巴和外淋巴。此外,KO支持细胞可塑性,并可能提供在特定条件下能够反分化为毛细胞的前体细胞储存库。结论:耳蜗功能失调或其支持细胞的延迟变性与听觉障碍有关,强调了该器官在正常耳蜗发育和听觉功能中的重要性。尽管它在一个多世纪前被发现,但需要进一步的研究来阐明KO对听觉成熟的分子机制,特别是在人类生理学上的贡献。
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来源期刊
Audiology Research
Audiology Research AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY-
CiteScore
2.30
自引率
23.50%
发文量
56
审稿时长
11 weeks
期刊介绍: The mission of Audiology Research is to publish contemporary, ethical, clinically relevant scientific researches related to the basic science and clinical aspects of the auditory and vestibular system and diseases of the ear that can be used by clinicians, scientists and specialists to improve understanding and treatment of patients with audiological and neurotological disorders.
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