Avraham Oshri, Hadas Yoav, Vald Lilach, Zisman Sophie, Schejter Adi, Visel Axel, Klar Avihu
Department of Medical Neurobiology, IMRIC, Hebrew University, Hadassah Medical School, Jerusalem, Israel.
Neural Dev. 2009 Jun 19;4:21. doi: 10.1186/1749-8104-4-21.
Lim-HD proteins control crucial aspects of neuronal differentiation, including subtype identity and axonal guidance. The Lim-HD proteins Lhx2/9 and Lhx1/5 are expressed in the dorsal spinal interneuron populations dI1 and dI2, respectively. While they are not required for cell fate acquisition, their role in patterning the axonal trajectory of dI1 and dI2 neurons remains incompletely understood.
Using newly identified dI1- and dI2-specific enhancers to trace axonal trajectories originating from these interneurons, we found that each population is subdivided into several distinct groups according to their axonal pathways. dI1 neurons project axons rostrally, either ipsi- or contra-laterally, while dI2 are mostly commissural neurons that project their axons rostrally and caudally. The longitudinal axonal tracks of each neuronal population self-fasciculate to form dI1- and dI2-specific bundles. The dI1 bundles are spatially located ventral relative to dI2 bundles. To examine the functional contribution of Lim-HD proteins to establishment of dI axonal projections, the Lim-HD code of dI neurons was altered by cell-specific ectopic expression. Expression of Lhx1 in dI1 neurons caused a repression of Lhx2/9 and imposed caudal projection to the caudal commissural dI1 neurons. Complementarily, when expressed in dI2 neurons, Lhx9 repressed Lhx1/5 and triggered a bias toward rostral projection in otherwise caudally projecting dI2 neurons, and ventral shift of the longitudinal axonal fascicule.
The Lim-HD proteins Lhx9 and Lhx1 serve as a binary switch in controlling the rostral versus caudal longitudinal turning of the caudal commissural axons. Lhx1 determines caudal turning and Lhx9 triggers rostral turning.
Lim-HD蛋白控制神经元分化的关键方面,包括亚型特性和轴突导向。Lim-HD蛋白Lhx2/9和Lhx1/5分别在背侧脊髓中间神经元群体dI1和dI2中表达。虽然它们不是细胞命运获得所必需的,但它们在塑造dI1和dI2神经元轴突轨迹模式中的作用仍未完全了解。
利用新鉴定的dI1和dI2特异性增强子来追踪源自这些中间神经元的轴突轨迹,我们发现每个群体根据其轴突通路被细分为几个不同的组。dI1神经元向头端投射轴突,可同侧或对侧投射,而dI2大多是连合神经元,其轴突向头端和尾端投射。每个神经元群体的纵向轴突束自我成束,形成dI1和dI2特异性束。dI1束在空间上位于dI2束的腹侧。为了研究Lim-HD蛋白对dI轴突投射建立的功能贡献,通过细胞特异性异位表达改变了dI神经元的Lim-HD编码。在dI1神经元中表达Lhx1导致Lhx2/9的抑制,并使尾侧连合dI1神经元向尾侧投射。互补地,当在dI2神经元中表达时,Lhx9抑制Lhx1/5,并在原本向尾侧投射的dI2神经元中引发向头端投射的偏向,以及纵向轴突束的腹侧移位。
Lim-HD蛋白Lhx9和Lhx1作为二元开关,控制尾侧连合轴突的头端与尾端纵向转向。Lhx1决定尾侧转向,Lhx9触发头端转向。