Chen Yin-Tzu, Young Tai-Horng, Wang Yu-Hsin, Huang Chih-Hsuan, Gao Yu-Yun, Huang Tsung-Wei
Department of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, Taipei, Taiwan.
Department of Otolaryngology, Far Eastern Memorial Hospital, Taipei, Taiwan.
Regen Ther. 2024 Nov 8;26:1058-1068. doi: 10.1016/j.reth.2024.10.014. eCollection 2024 Jun.
Sensorineural olfactory dysfunction significantly impairs the life quality of patients but without effective treatments to date. Orexin is a neurotrophic factor activates neuronal network activity. However, it is still unknown whether orexin can promote differentiation in human olfactory sensory neurons (OSNs). This study seeks to explore the impact of orexin on the differentiation of human olfactory neuroepithelial cells (HONCs).
The primary olfactory epithelium cells were cultured with or without orexin-A. The neural maturation-related and functional proteins were analyzed through immunofluorescence staining and Western blot. The function of HONCs were evaluated through the synaptic vesicle recycling assay.
The results showed that HONCs in the orexin-A group expressed higher levels of stage-specific markers, including achaete-scute homolog 1, βIII-tubulin, and olfactory marker protein. Additionally, more components of signaling transduction pathways compared to the control group. The orexin-A-mediated differentiation of OSN effect can be nullified with dual orexin receptor antagonist suvorexant and the selective orexin receptor type 1 antagonist SB674042, instead of selective orexin receptor type 2 antagonist TCS-OX2-29.
Orexin-A elevates the expression of protein markers in human olfactory neuronal progenitor cells to stimulate the differentiation of OSN and enhances the formation of components of the olfactory-specific signaling transduction pathway via orexin receptor type 1.
感觉神经性嗅觉功能障碍严重损害患者的生活质量,但迄今为止尚无有效的治疗方法。食欲素是一种能激活神经网络活动的神经营养因子。然而,食欲素是否能促进人嗅觉感觉神经元(OSNs)的分化仍不清楚。本研究旨在探讨食欲素对人嗅觉神经上皮细胞(HONCs)分化的影响。
将原代嗅觉上皮细胞在有或无食欲素-A的情况下进行培养。通过免疫荧光染色和蛋白质印迹分析神经成熟相关蛋白和功能蛋白。通过突触小泡循环试验评估HONCs的功能。
结果显示,食欲素-A组的HONCs表达了更高水平的阶段特异性标志物,包括achaete-scute同源物1、βIII-微管蛋白和嗅觉标记蛋白。此外,与对照组相比,信号转导通路的成分更多。食欲素-A介导的OSN分化作用可被双重食欲素受体拮抗剂苏沃雷生和选择性食欲素受体1型拮抗剂SB674042消除,而不是选择性食欲素受体2型拮抗剂TCS-OX2-29。
食欲素-A提高人嗅觉神经元祖细胞中蛋白质标志物的表达,以刺激OSN的分化,并通过食欲素受体1型增强嗅觉特异性信号转导通路成分的形成。