He Jinling, Lu Shunlan, Mo Weijian, Tang Anzhou, Tan Songhua, Liu Lei, Fang Qin, Xie Lihong
Department of Otorhinolaryngology Head and Neck Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Key Laboratory of Early Prevention and Treatment for High Frequency Tumor, Ministry of Education, Nanning, China.
Microsc Res Tech. 2022 May;85(5):1837-1844. doi: 10.1002/jemt.24045. Epub 2021 Dec 27.
This study aimed to observe the ultrastructure on the surface of the inner ear of a normal tree shrew using scanning electron microscope (SEM). The specimens of cochlea, macula utriculi, macula sacculi, and crista ampullaris of the normal adult tree shrew were collected and observed by SEM. We used immunofluorescence for cochlear protein Atoh1 staining. We observed that cochlea of the tree shrew is centered on the cochlear axis, circling about 3.5 times from bottom to top of the cochlea. The organ of Corti is located between medial and lateral grooves, including inner and outer hair cells as well as supporting cells. Maculae staticae include macula of saccule and macula of utricle, and the surface of macula is covered with a large number of otoliths. We found a gelatinous layer below the otoliths, followed by the layer of the honeycomb structure. The hair cell cilia of macula and crista ampullaris include one kinocilium and more stereocilia. There is no obvious cross structure but numerous hair cell cilia on semicircular canal crista ampullaris. Immunofluorescence staining showed that protein Atoh1 is mainly distributed in the nucleus of the cochlea's inner and outer hair cells. The observation of the inner ear structure under SEM elucidate the fine surface morphological structure of the entire cochlea, the vestibular maculae staticae, and crista ampullaris, providing new insight into the structure and function of the inner ear of tree shrew. HIGHLIGHTS: This article is the first to describe the inner ear ultrastructure of a small primate tree shrew by scanning electron microscopy (SEM). Under an SEM, the phalangeal processes of Deiter cells in tree shrews were observed to be connected to the tip of a neighboring hair cell, which was different from that of Deiters' cells in guinea pigs, and this crossed one hair cell, and connected to the tip of the third hair cell. It was observed that the crista ampullaris of tree shrews were horseshoe-shaped, and similar to that of humans and monkeys, this had no obvious "cross-shaped hump" structure. Tree shrew's ABR threshold value curve conforms to the mammalian U-shaped curve, wave III is the main wave of ARB, its sensory frequency may be higher 8 kHz, and the characteristics of the stereocilia of tree shrew we have observed may be related to the perception of higher frequency hearing.
本研究旨在利用扫描电子显微镜(SEM)观察正常树鼩内耳表面的超微结构。收集正常成年树鼩的耳蜗、椭圆囊斑、球囊斑和壶腹嵴标本,并用扫描电子显微镜进行观察。我们采用免疫荧光法对耳蜗蛋白Atoh1进行染色。我们观察到,树鼩的耳蜗以蜗轴为中心,从耳蜗底部到顶部盘旋约3.5圈。柯蒂氏器位于内侧沟和外侧沟之间,包括内毛细胞、外毛细胞以及支持细胞。静态斑包括球囊斑和椭圆囊斑,其表面覆盖有大量耳石。我们在耳石下方发现一层凝胶层,其后是蜂窝结构层。椭圆囊斑和壶腹嵴的毛细胞纤毛包括一根动纤毛和更多的静纤毛。半规管壶腹嵴上没有明显的交叉结构,但有大量毛细胞纤毛。免疫荧光染色显示,蛋白Atoh1主要分布在耳蜗内、外毛细胞的细胞核中。通过扫描电子显微镜对内耳结构的观察阐明了整个耳蜗、前庭静态斑和壶腹嵴的精细表面形态结构,为树鼩内耳的结构和功能提供了新的见解。要点:本文首次通过扫描电子显微镜(SEM)描述了小型灵长类动物树鼩的内耳超微结构。在扫描电子显微镜下观察到,树鼩的Dieters细胞的指状突与相邻毛细胞的顶端相连,这与豚鼠的Dieters细胞不同,豚鼠的Dieters细胞穿过一个毛细胞,并与第三个毛细胞的顶端相连。观察到树鼩的壶腹嵴呈马蹄形,与人类和猴子的相似,没有明显的“十字形隆起”结构。树鼩的听性脑干反应(ABR)阈值曲线符合哺乳动物的U形曲线,波III是ABR的主波,其感觉频率可能高于8kHz,我们观察到的树鼩静纤毛的特征可能与高频听力的感知有关。