Xu Yinfang, Zhang Yan, Lundberg Yunxia Wang
Vestibular Genetics Laboratory, Center for Sensory Neuroscience, Boys Town National Research Hospital, Omaha, Nebraska, 68131, USA.
Cell Electrophysiology Laboratory, Shanghai Research Center of Acupuncture and Meridians, Shanghai, 201203, China.
Genesis. 2016 Dec;54(12):613-625. doi: 10.1002/dvg.22990. Epub 2016 Nov 12.
Otoconia are minute biocrystals composed of glycoproteins, proteoglycans, and CaCO , and are indispensable for sensory processing in the utricle and saccule. Otoconia abnormalities and degeneration can cause or facilitate crystal dislocation to the ampulla, leading to vertigo and imbalance in humans. In order to better understand the molecular mechanism controlling otoconia formation and maintenance, we have examined the spatial and temporal expression differences of otoconial genes in the mouse inner ear at developmental, mature and aging stages using whole transcriptome sequencing (RNA-Seq) and quantitative RT-PCR. We show that the expression levels of most otoconial genes are much higher in the utricle and saccule compared with other inner ear tissues before postnatal stages in C57Bl/6J mice, and the expression of a few of these genes is restricted to the embryonic utricle and saccule. After the early postnatal stages, expression of all otoconial genes in the utricle and saccule is drastically reduced, while a few genes gain expression dominance in the aging ampulla, indicating a potential for ectopic debris formation in the latter tissue at old ages. The data suggest that the expression of otoconial genes is tightly regulated spatially and temporally during developmental stages and can become unregulated at aging stages. Birth Defects Research (Part A) 106:613-625, 2016. © 2016 Wiley Periodicals, Inc.
耳石是由糖蛋白、蛋白聚糖和碳酸钙组成的微小生物晶体,对于椭圆囊和球囊的感觉处理必不可少。耳石异常和退化会导致或促使晶体移位至壶腹,从而引起人类眩晕和平衡失调。为了更好地理解控制耳石形成和维持的分子机制,我们使用全转录组测序(RNA-Seq)和定量RT-PCR检测了小鼠内耳在发育、成熟和衰老阶段耳石相关基因的时空表达差异。我们发现,在C57Bl/6J小鼠出生后阶段之前,与其他内耳组织相比,椭圆囊和球囊中大多数耳石相关基因的表达水平要高得多,其中一些基因的表达仅限于胚胎期的椭圆囊和球囊。出生后早期阶段之后,椭圆囊和球囊中所有耳石相关基因的表达急剧下降,而一些基因在衰老的壶腹中获得表达优势,这表明老年时后一组织中可能会形成异位碎片。数据表明,耳石相关基因的表达在发育阶段受到严格的时空调控,而在衰老阶段可能会失控。《出生缺陷研究(A部分)》106:613 - 625,2016年。© 2016威利期刊公司。