State Key Laboratory of Pharmaceutical Biotechnology, Department of Otolaryngology Head and Neck Surgery, Jiangsu Provincial Key Medical Discipline (Laboratory), The Affiliated Drum Tower Hospital of Medical School, Model Animal Research Center of Medical School, Nanjing University, Nanjing, 210061, China; MOE Key Laboratory of Model Animal for Disease Study, Jiangsu Key Laboratory of Molecular Medicine, National Resource Center for Mutant Mice of China, Nanjing University, Nanjing, 210061, China.
State Key Laboratory of Pharmaceutical Biotechnology, Department of Otolaryngology Head and Neck Surgery, Jiangsu Provincial Key Medical Discipline (Laboratory), The Affiliated Drum Tower Hospital of Medical School, Model Animal Research Center of Medical School, Nanjing University, Nanjing, 210061, China; MOE Key Laboratory of Model Animal for Disease Study, Jiangsu Key Laboratory of Molecular Medicine, National Resource Center for Mutant Mice of China, Nanjing University, Nanjing, 210061, China; Research Institute of Otolaryngology, No. 321 Zhongshan Road, Nanjing, 210061, China.
Biochem Biophys Res Commun. 2024 Apr 16;704:149704. doi: 10.1016/j.bbrc.2024.149704. Epub 2024 Feb 21.
Ribbon synapses in the cochlear hair cells are subject to extensive pruning and maturation processes before hearing onset. Previous studies have highlighted the pivotal role of thyroid hormone (TH) in this developmental process, yet the detailed mechanisms are largely unknown. In this study, we found that the thyroid hormone receptor α (Thrα) is expressed in both sensory epithelium and spiral ganglion neurons in mice. Hypothyroidism, induced by Pax8 gene knockout, significantly delays the synaptic pruning during postnatal development in mice. Detailed spatiotemporal analysis of ribbon synapse distribution reveals that synaptic maturation involves not only ribbon pruning but also their migration, both of which are notably delayed in the cochlea of Pax8 knockout mice. Intriguingly, postnatal hyperthyroidism, induced by intraperitoneal injections of liothyronine sodium (T3), accelerates the pruning of ribbon synapses to the mature state without affecting the auditory functions. Our findings suggest that thyroid hormone does not play a deterministic role but rather controls the timing of cochlear ribbon synapse maturation.
在听力起始之前,耳蜗毛细胞中的带状突触经历广泛的修剪和成熟过程。先前的研究强调了甲状腺激素 (TH) 在这个发育过程中的关键作用,但详细的机制在很大程度上尚不清楚。在这项研究中,我们发现甲状腺激素受体 α (Thrα) 在小鼠的感觉上皮和螺旋神经节神经元中均有表达。Pax8 基因敲除诱导的甲状腺功能减退症显著延迟了小鼠出生后发育过程中的突触修剪。带状突触分布的详细时空分析表明,突触成熟不仅涉及到带状突触的修剪,还涉及到它们的迁移,而这两者在 Pax8 敲除小鼠的耳蜗中明显延迟。有趣的是,通过腹腔注射左甲状腺素钠 (T3) 诱导的产后甲状腺功能亢进加速了带状突触向成熟状态的修剪,而不影响听觉功能。我们的研究结果表明,甲状腺激素不起决定性作用,而是控制耳蜗带状突触成熟的时机。