Liu Jingwen, Zhang Xu, Zhang Qingchen, Wang Rongrong, Ma Jingyu, Bai Xiaohui, Wang Dawei
Department of Clinical Laboratory, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Ophthalmology, Jinan Second People's Hospital, Jinan, China.
Front Cell Neurosci. 2022 Nov 24;16:1065309. doi: 10.3389/fncel.2022.1065309. eCollection 2022.
Mutations in lipoxygenase homology domain 1 () cause autosomal recessive inheritance, leading to high-frequency and intermediate-frequency hearing losses in patients. To date, studies on the localization of gene expression are limited. In this study, we aimed to observe the expressions of in zebrafish, C57BL/6 murine cochlea, and HEI-OC1 cells.
The expression of in the auditory system of zebrafish was explored by hybridization experiments of zebrafish embryos. The expression of in cochlear and HEI-OC1 cells of C57BL/6 mice was analyzed by immunofluorescence staining. Confocal microscopic in vivo imaging was used to detect the number and morphological characteristics of lateral line neuromasts and inner ear hair cells in zebrafish that knocked down gene. The effect of knockdown gene on the development of zebrafish otolith and semicircular canal was observed using microscopic. Transcriptome sequencing was used to identify downstream molecules and associated signaling pathways and validated by western blotting, immunostaining, and rescue experiments.
Results of the hybridization with zebrafish embryos at different time points showed that was expressed in zebrafish at the inner ear and olfactory pores, while the immunostaining showed that was expressed in both C57BL/6 mouse cochlea and HEI-OC1 cells. Loxhd1b knockdown causes a decrease in the number of spinal and lateral line neuromasts in the inner ear of zebrafish, accompanied by weakened hearing function, and also leads to developmental defects of otoliths and ear follicles. The results of transcriptomics analysis revealed the downstream molecule brain-derived neurotrophic factor (BDNF) and verified that and BDNF regulate the formation of zebrafish hair cells by synergistic regulation of BDNF/TrkB/ERK pathway based on western blotting, immunostaining, and rescue experiments.
This was the first time that the BDNF/TrkB/ERK pathway was identified to play a critical role in the molecular regulation of the development of zebrafish hair cells and the auditory development by .
脂氧合酶同源结构域1(Loxhd1)突变导致常染色体隐性遗传,致使患者出现高频和中频听力损失。迄今为止,关于Loxhd1基因表达定位的研究有限。在本研究中,我们旨在观察Loxhd1在斑马鱼、C57BL/6小鼠耳蜗及HEI-OC1细胞中的表达情况。
通过斑马鱼胚胎的原位杂交实验探究Loxhd1在斑马鱼听觉系统中的表达。采用免疫荧光染色分析Loxhd1在C57BL/6小鼠耳蜗及HEI-OC1细胞中的表达。利用共聚焦显微镜体内成像检测敲低Loxhd1基因的斑马鱼侧线神经丘及内耳毛细胞的数量和形态特征。使用显微镜观察敲低Loxhd1基因对斑马鱼耳石和半规管发育的影响。采用转录组测序鉴定下游分子及相关信号通路,并通过蛋白质免疫印迹、免疫染色及拯救实验进行验证。
不同时间点斑马鱼胚胎的原位杂交结果显示,Loxhd1在斑马鱼的内耳和嗅孔中表达,而免疫染色表明Loxhd1在C57BL/6小鼠耳蜗及HEI-OC1细胞中均有表达。敲低Loxhd1b会导致斑马鱼内耳中脊髓和侧线神经丘数量减少,同时听力功能减弱,还会导致耳石和耳泡发育缺陷。转录组学分析结果揭示了下游分子脑源性神经营养因子(BDNF),并基于蛋白质免疫印迹、免疫染色及拯救实验证实Loxhd1和BDNF通过协同调节BDNF/TrkB/ERK通路来调控斑马鱼毛细胞的形成。
首次证实BDNF/TrkB/ERK通路在Loxhd1对斑马鱼毛细胞发育及听觉发育的分子调控中起关键作用。