State Key Laboratory of Bioelectronics, Department of Otolaryngology Head and Neck Surgery, Zhongda Hospital, School of Life Sciences and Technology, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, 210096, China.
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, China.
Cell Mol Life Sci. 2022 Feb 26;79(3):154. doi: 10.1007/s00018-022-04164-x.
The cochlea is an important sensory organ for both balance and sound perception, and the formation of the cochlea is a complex developmental process. The development of the mouse cochlea begins on embryonic day (E)9 and continues until postnatal day (P)21 when the hearing system is considered mature. Small extracellular vesicles (sEVs), with a diameter ranging from 30 to 200 nm, have been considered a significant medium for information communication in both physiological and pathological processes. However, there are no studies exploring the role of sEVs in the development of the cochlea. Here, we isolated tissue-derived sEVs from the cochleae of FVB mice at P3, P7, P14, and P21 by ultracentrifugation. These sEVs were first characterized by transmission electron microscopy, nanoparticle tracking analysis, and western blotting. Next, we used small RNA-seq and mass spectrometry to characterize the microRNA transcriptomes and proteomes of cochlear sEVs from mice at different ages. Many microRNAs and proteins were discovered to be related to inner ear development, anatomical structure development, and auditory nervous system development. These results all suggest that sEVs exist in the cochlea and are likely to be essential for the normal development of the auditory system. Our findings provide many sEV microRNA and protein targets for future studies of the roles of cochlear sEVs.
耳蜗是平衡和声音感知的重要感觉器官,耳蜗的形成是一个复杂的发育过程。小鼠耳蜗的发育始于胚胎第 9 天(E),并持续到出生后第 21 天(P),此时听觉系统被认为已经成熟。小细胞外囊泡(sEVs)的直径范围为 30 至 200nm,被认为是生理和病理过程中信息交流的重要介质。然而,目前还没有研究探索 sEVs 在耳蜗发育中的作用。在这里,我们通过超速离心从 FVB 小鼠 P3、P7、P14 和 P21 的耳蜗中分离出组织衍生的 sEVs。这些 sEVs 首先通过透射电子显微镜、纳米颗粒跟踪分析和 Western blot 进行表征。接下来,我们使用小 RNA-seq 和质谱法来表征不同年龄小鼠耳蜗 sEVs 的 microRNA 转录组和蛋白质组。发现许多 microRNAs 和蛋白质与内耳发育、解剖结构发育和听觉神经系统发育有关。这些结果均表明 sEVs 存在于耳蜗中,并且可能对听觉系统的正常发育至关重要。我们的发现为未来研究耳蜗 sEVs 的作用提供了许多 sEV microRNA 和蛋白质靶标。