Paplou Vasiliki Georgia, Schubert Nick M A, van Tuinen Marcel, Vijayakumar Sarath, Pyott Sonja J
Department of Otorhinolaryngology and Head/Neck Surgery, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Graduate School of Medical Sciences Research, School of Behavioural and Cognitive Neurosciences, University of Groningen, 9713 AV Groningen, The Netherlands.
Biomolecules. 2023 Sep 21;13(9):1429. doi: 10.3390/biom13091429.
Age-related loss of vestibular function and hearing are common disorders that arise from the loss of function of the inner ear and significantly decrease quality of life. The underlying pathophysiological mechanisms are poorly understood and difficult to investigate in humans. Therefore, our study examined young (1.5-month-old) and old (24-month-old) C57BL/6 mice, utilizing physiological, histological, and transcriptomic methods. Vestibular sensory-evoked potentials revealed that older mice had reduced wave I amplitudes and delayed wave I latencies, indicating reduced vestibular function. Immunofluorescence and image analysis revealed that older mice exhibited a significant decline in type I sensory hair cell density, particularly in hair cells connected to dimorphic vestibular afferents. An analysis of gene expression in the isolated vestibule revealed the upregulation of immune-related genes and the downregulation of genes associated with ossification and nervous system development. A comparison with the isolated cochlear sensorineural structures showed similar changes in genes related to immune response, chondrocyte differentiation, and myelin formation. These findings suggest that age-related vestibular hypofunction is linked to diminished peripheral vestibular responses, likely due to the loss of a specific subpopulation of hair cells and calyceal afferents. The upregulation of immune- and inflammation-related genes implies that inflammation contributes to these functional and structural changes. Furthermore, the comparison of gene expression between the vestibule and cochlea indicates both shared and distinct mechanisms contributing to age-related vestibular and hearing impairments. Further research is necessary to understand the mechanistic connection between inflammation and age-related balance and hearing disorders and to translate these findings into clinical treatment strategies.
与年龄相关的前庭功能丧失和听力丧失是常见疾病,源于内耳功能丧失,显著降低生活质量。其潜在的病理生理机制尚不清楚,且在人类中难以研究。因此,我们的研究利用生理学、组织学和转录组学方法,对年轻(1.5月龄)和年老(24月龄)的C57BL/6小鼠进行了研究。前庭感觉诱发电位显示,老年小鼠的I波振幅降低,I波潜伏期延长,表明前庭功能下降。免疫荧光和图像分析显示,老年小鼠的I型感觉毛细胞密度显著下降,尤其是与双态前庭传入神经相连的毛细胞。对分离出的前庭进行基因表达分析,发现免疫相关基因上调,与骨化和神经系统发育相关的基因下调。与分离出的耳蜗感觉神经结构进行比较,发现与免疫反应、软骨细胞分化和髓鞘形成相关的基因有类似变化。这些发现表明,与年龄相关的前庭功能减退与外周前庭反应减弱有关,可能是由于特定亚群的毛细胞和杯状传入神经的丧失。免疫和炎症相关基因的上调意味着炎症促成了这些功能和结构变化。此外,前庭和耳蜗之间基因表达的比较表明,炎症在与年龄相关的前庭和听力障碍中发挥着共同和独特的作用。有必要进一步研究炎症与年龄相关的平衡和听力障碍之间的机制联系,并将这些发现转化为临床治疗策略。