Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel; Department of Orthopedic Surgery, Assaf HaRofeh Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Zerrifin 70300, Israel.
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.
Dev Cell. 2017 Aug 21;42(4):388-399.e3. doi: 10.1016/j.devcel.2017.07.022.
Maintaining posture requires tight regulation of the position and orientation of numerous spinal components. Yet, surprisingly little is known about this regulatory mechanism, whose failure may result in spinal deformity as in adolescent idiopathic scoliosis. Here, we use genetic mouse models to demonstrate the involvement of proprioception in regulating spine alignment. Null mutants for Runx3 transcription factor, which lack TrkC neurons connecting between proprioceptive mechanoreceptors and spinal cord, developed peripubertal scoliosis not preceded by vertebral dysplasia or muscle asymmetry. Deletion of Runx3 in the peripheral nervous system or specifically in peripheral sensory neurons, or of enhancer elements driving Runx3 expression in proprioceptive neurons, induced a similar phenotype. Egr3 knockout mice, lacking muscle spindles, but not Golgi tendon organs, displayed a less severe phenotype, suggesting that both receptor types may be required for this regulatory mechanism. These findings uncover a central role for the proprioceptive system in maintaining spinal alignment.
维持姿势需要严格调节众多脊柱成分的位置和方向。然而,人们对这个调节机制知之甚少,其失效可能导致脊柱畸形,如青少年特发性脊柱侧凸。在这里,我们使用遗传小鼠模型来证明本体感觉在调节脊柱排列中的作用。缺乏连接本体感受机械感受器和脊髓的感觉神经元的转录因子 Runx3 缺失突变体,在青春期前出现脊柱侧凸,而不是以前椎体发育不良或肌肉不对称为特征。外周神经系统或专门在周围感觉神经元中缺失 Runx3,或缺失驱动本体感受神经元中 Runx3 表达的增强子元件,都会诱导出类似的表型。缺乏肌梭但不缺乏高尔基肌腱器官的 Egr3 敲除小鼠表现出较轻的表型,这表明这两种受体类型可能都需要这种调节机制。这些发现揭示了本体感觉系统在维持脊柱排列中的核心作用。