Department of Neuroscience, Howard Hughes Medical Institute, Kavli Institute for Brain Science, Columbia University, New York, NY 10032, USA.
Neuron. 2013 Mar 20;77(6):1055-68. doi: 10.1016/j.neuron.2013.01.015.
The organization of spinal reflex circuits relies on the specification of distinct classes of proprioceptive sensory neurons (pSN), but the factors that drive such diversity remain unclear. We report here that pSNs supplying distinct skeletal muscles differ in their dependence on the ETS transcription factor Etv1 for their survival and differentiation. The status of Etv1-dependence is linked to the location of proprioceptor muscle targets: pSNs innervating hypaxial and axial muscles depend critically on Etv1 for survival, whereas those innervating certain limb muscles are resistant to Etv1 inactivation. The level of NT3 expression in individual muscles correlates with Etv1-dependence and the loss of pSNs triggered by Etv1 inactivation can be prevented by elevating the level of muscle-derived NT3-revealing a TrkC-activated Etv1-bypass pathway. Our findings support a model in which the specification of aspects of pSN subtype character is controlled by variation in the level of muscle NT3 expression and signaling.
脊髓反射回路的组织依赖于特定类别本体感觉神经元(pSN)的特异性,但驱动这种多样性的因素仍不清楚。我们在这里报告,供应不同骨骼肌的 pSN 在其生存和分化对 ETS 转录因子 Etv1 的依赖性方面存在差异。Etv1 依赖性的状态与本体感受器肌肉靶位的位置有关:支配腹侧和轴性肌肉的 pSN 对 Etv1 的生存至关重要,而支配某些肢体肌肉的 pSN 则对 Etv1 失活有抗性。个体肌肉中 NT3 的表达水平与 Etv1 依赖性相关,并且由 Etv1 失活引发的 pSN 丧失可以通过提高肌肉衍生的 NT3 水平来预防,这揭示了一种 TrkC 激活的 Etv1 旁路途径。我们的研究结果支持这样一种模型,即 pSN 亚型特征的某些方面的特异性是由肌肉 NT3 表达和信号的水平变化控制的。