Kohl Ayelet, Marquardt Till, Klar Avihu, Sela-Donenfeld Dalit
Koret School of Veterinary Medicine, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot 76100, Israel.
Developmental Neurobiology Laboratory, European Neuroscience Institute, Göttingen 37077, Germany, and.
J Neurosci. 2015 Feb 11;35(6):2596-611. doi: 10.1523/JNEUROSCI.2699-14.2015.
Hindbrain dorsal interneurons (HDIs) are implicated in receiving, processing, integrating, and transmitting sensory inputs from the periphery and spinal cord, including the vestibular, auditory, and proprioceptive systems. During development, multiple molecularly defined HDI types are set in columns along the dorsoventral axis, before migrating along well-defined trajectories to generate various brainstem nuclei. Major brainstem functions rely on the precise assembly of different interneuron groups and higher brain domains into common circuitries. Yet, knowledge regarding interneuron axonal patterns, synaptic targets, and the transcriptional control that govern their connectivity is sparse. The dB1 class of HDIs is formed in a district dorsomedial position along the hindbrain and gives rise to the inferior olive nuclei, dorsal cochlear nuclei, and vestibular nuclei. dB1 interneurons express various transcription factors (TFs): the pancreatic transcription factor 1a (Ptf1a), the homeobox TF-Lbx1 and the Lim-homeodomain (Lim-HD), and TF Lhx1 and Lhx5. To decipher the axonal and synaptic connectivity of dB1 cells, we have used advanced enhancer tools combined with conditional expression systems and the PiggyBac-mediated DNA transposition system in avian embryos. Multiple ipsilateral and contralateral axonal projections were identified ascending toward higher brain centers, where they formed synapses in the Purkinje cerebellar layer as well as at discrete midbrain auditory and vestibular centers. Decoding the mechanisms that instruct dB1 circuit formation revealed a fundamental role for Lim-HD proteins in regulating their axonal patterns, synaptic targets, and neurotransmitter choice. Together, this study provides new insights into the assembly and heterogeneity of HDIs connectivity and its establishment through the central action of Lim-HD governed programs.
后脑背侧中间神经元(HDI)参与接收、处理、整合和传递来自外周和脊髓的感觉输入,包括前庭、听觉和本体感觉系统。在发育过程中,多种分子定义的HDI类型沿背腹轴排列成列,然后沿着明确的轨迹迁移,以形成各种脑干核。主要的脑干功能依赖于不同中间神经元组和更高脑区精确组装成共同的神经回路。然而,关于中间神经元轴突模式、突触靶点以及控制其连接性的转录调控的知识却很匮乏。HDI的dB1类在沿后脑的背内侧特定位置形成,并产生下橄榄核、背侧耳蜗核和前庭核。dB1中间神经元表达多种转录因子(TF):胰腺转录因子1a(Ptf1a)、同源盒TF-Lbx1和Lim同源结构域(Lim-HD),以及TF Lhx1和Lhx5。为了解析dB1细胞的轴突和突触连接性,我们在鸡胚中使用了先进的增强子工具,结合条件表达系统和PiggyBac介导的DNA转座系统。我们确定了多个同侧和对侧轴突投射向上延伸至更高脑区中心,在那里它们在小脑浦肯野层以及离散的中脑听觉和前庭中心形成突触。对指导dB1回路形成机制的解码揭示了Lim-HD蛋白在调节其轴突模式、突触靶点和神经递质选择方面的基本作用。总之,这项研究为HDI连接性的组装和异质性以及通过Lim-HD调控程序的中枢作用建立连接性提供了新的见解。