Kagoshima Hiroki, Ohnishi Hiroe, Yamamoto Ryosuke, Yasumoto Akiyoshi, Tona Yosuke, Nakagawa Takayuki, Omori Koichi, Yamamoto Norio
Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Biological Sciences, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, Ontario M4N 3M5, Canada.
J Neurosci. 2024 Feb 14;44(7):e1060232023. doi: 10.1523/JNEUROSCI.1060-23.2023.
Early B-cell factor 1 (EBF1) is a basic helix-loop-helix transcription factor essential for the differentiation of various tissues. Our single-cell RNA sequencing data suggest that is expressed in the sensory epithelium of the mouse inner ear. Here, we found that the murine gene and its protein are expressed in the prosensory domain of the inner ear, medial region of the cochlear duct floor, otic mesenchyme, and cochleovestibular ganglion. deletion in mice results in incomplete formation of the spiral limbus and scala tympani, increased number of cells in the organ of Corti and Kölliker's organ, and aberrant course of the spiral ganglion axons. deletion in the mouse cochlear epithelia caused the proliferation of SOX2-positive cochlear cells at E13.5, indicating that EBF1 suppresses the proliferation of the prosensory domain and cells of Kölliker's organ to facilitate the development of appropriate numbers of hair and supporting cells. Furthermore, mice with deletion of cochlear epithelium-specific showed poor postnatal hearing function. Our results suggest that is essential for normal auditory function in mammals.
早期B细胞因子1(EBF1)是一种对多种组织分化至关重要的碱性螺旋-环-螺旋转录因子。我们的单细胞RNA测序数据表明,其在小鼠内耳的感觉上皮中表达。在此,我们发现小鼠的该基因及其蛋白在内耳的前感觉区域、蜗管底部内侧区域、耳间质和蜗神经节中表达。小鼠中的该基因缺失导致螺旋缘和鼓阶形成不完全,柯蒂氏器和科蒂器中的细胞数量增加,以及螺旋神经节轴突走行异常。小鼠耳蜗上皮中的该基因缺失在胚胎第13.5天导致SOX2阳性耳蜗细胞增殖,表明EBF1抑制前感觉区域和科蒂器细胞的增殖,以促进适量毛细胞和支持细胞的发育。此外,耳蜗上皮特异性该基因缺失的小鼠出生后的听力功能较差。我们的结果表明,该基因对哺乳动物的正常听觉功能至关重要。