Kang Yun Jin, Jang David W, Kim Do Hyun
Department of Otolaryngology-Head and Neck Surgery, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Head and Neck Surgery & Communication Sciences, Duke University School of Medicine, Durham, NC, USA.
J Rhinol. 2025 Jul;32(2):76-83. doi: 10.18787/jr.2025.00013. Epub 2025 Jul 22.
Olfactory dysfunction affects many individuals and may result from infections, trauma, neurodegenerative diseases, or genetic disorders. Unlike most neurons in the mammalian nervous system, olfactory sensory neurons (OSNs) continuously regenerate throughout life, a process facilitated by specialized stem cell niches in the olfactory epithelium. Horizontal basal cells are typically dormant under normal conditions but become activated following injury, differentiating into globose basal cells (GBCs) and other cell types. GBCs serve as the primary source for OSN regeneration and are regulated by key transcription factors such as Sox2, Pax6, and Ascl1. Olfactory ensheathing cells play a vital role in regeneration by guiding newly formed axons toward the olfactory bulb and secreting neurotrophic factors, including glial cell-derived neurotrophic factor. In addition, the olfactory bulb synthesizes trophic factors like brain-derived neurotrophic factor and nerve growth factor, which support neuronal survival and integration. Despite this intrinsic regenerative capacity, many cases of olfactory dysfunction remain challenging to treat. Current therapeutic strategies include corticosteroids, biologics, surgical interventions, and olfactory training, although their effectiveness varies. Advances in molecular and cellular research have provided insights into the regulatory mechanisms of olfactory neurogenesis, underscoring the need for further exploration of stem cell activation, neuronal survival, and olfactory circuit reorganization. Future research should focus on optimizing regenerative therapies-including stem cell-based approaches and neurotrophic factor modulation-to improve outcomes for patients with severe olfactory impairment.
嗅觉功能障碍影响着许多人,其可能由感染、创伤、神经退行性疾病或遗传疾病引起。与哺乳动物神经系统中的大多数神经元不同,嗅觉感觉神经元(OSN)在整个生命过程中持续再生,这一过程由嗅觉上皮中的特殊干细胞微环境所促进。水平基底细胞在正常情况下通常处于休眠状态,但在受伤后会被激活,分化为球状基底细胞(GBC)和其他细胞类型。GBC是OSN再生的主要来源,并受Sox2、Pax6和Ascl1等关键转录因子的调控。嗅觉鞘细胞在再生过程中起着至关重要的作用,它通过引导新形成的轴突朝向嗅球并分泌神经营养因子(包括胶质细胞源性神经营养因子)来发挥作用。此外,嗅球会合成诸如脑源性神经营养因子和神经生长因子等营养因子,这些因子支持神经元的存活和整合。尽管具有这种内在的再生能力,但许多嗅觉功能障碍病例的治疗仍然具有挑战性。目前的治疗策略包括使用皮质类固醇、生物制剂、手术干预和嗅觉训练,尽管它们的效果各不相同。分子和细胞研究的进展为嗅觉神经发生的调控机制提供了见解,强调了进一步探索干细胞激活、神经元存活和嗅觉回路重组的必要性。未来的研究应专注于优化再生疗法,包括基于干细胞的方法和神经营养因子调节,以改善严重嗅觉障碍患者的治疗效果。