Hilde Kathryn L, Levine Ariel J, Hinckley Christopher A, Hayashi Marito, Montgomery Jessica M, Gullo Miriam, Driscoll Shawn P, Grosschedl Rudolf, Kohwi Yoshinori, Kohwi-Shigematsu Terumi, Pfaff Samuel L
Gene Expression Laboratory and the Howard Hughes Medical Institute, Salk Institute for Biological Studies, 10010 North Torrey Pines, La Jolla, CA, 92037, USA.
Max Planck Institute of Immunobiology and Epigenetics, Department of Cellular and Molecular Immunology, 79108 Freiburg, Germany.
Neuron. 2016 Aug 17;91(4):763-776. doi: 10.1016/j.neuron.2016.07.014. Epub 2016 Jul 28.
Motor behaviors such as walking or withdrawing the limb from a painful stimulus rely upon integrative multimodal sensory circuitry to generate appropriate muscle activation patterns. Both the cellular components and the molecular mechanisms that instruct the assembly of the spinal sensorimotor system are poorly understood. Here we characterize the connectivity pattern of a sub-population of lamina V inhibitory sensory relay neurons marked during development by the nuclear matrix and DNA binding factor Satb2 (ISR(Satb2)). ISR(Satb2) neurons receive inputs from multiple streams of sensory information and relay their outputs to motor command layers of the spinal cord. Deletion of the Satb2 transcription factor from ISR(Satb2) neurons perturbs their cellular position, molecular profile, and pre- and post-synaptic connectivity. These alterations are accompanied by abnormal limb hyperflexion responses to mechanical and thermal stimuli and during walking. Thus, Satb2 is a genetic determinant that mediates proper circuit development in a core sensory-to-motor spinal network.
诸如行走或从疼痛刺激中撤回肢体等运动行为依赖于整合的多模态感觉回路来产生适当的肌肉激活模式。指导脊髓感觉运动系统组装的细胞成分和分子机制目前仍知之甚少。在这里,我们描述了在发育过程中由核基质和DNA结合因子Satb2标记的V层抑制性感觉中继神经元亚群的连接模式(ISR(Satb2))。ISR(Satb2)神经元接收来自多个感觉信息流的输入,并将其输出传递到脊髓的运动指令层。从ISR(Satb2)神经元中删除Satb2转录因子会扰乱它们的细胞位置、分子特征以及突触前和突触后的连接。这些改变伴随着对机械和热刺激以及行走过程中肢体异常过度屈曲反应。因此,Satb2是一种遗传决定因素,介导了核心感觉-运动脊髓网络中适当的回路发育。