Shen Hung-Chang, Chu Sao-Yu, Hsu Tsai-Chi, Wang Chun-Han, Lin I-Ya, Yu Hung-Hsiang
Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.
PLoS Genet. 2017 Apr 27;13(4):e1006751. doi: 10.1371/journal.pgen.1006751. eCollection 2017 Apr.
Elucidating how appropriate neurite patterns are generated in neurons of the olfactory system is crucial for comprehending the construction of the olfactory map. In the Drosophila olfactory system, projection neurons (PNs), primarily derived from four neural stem cells (called neuroblasts), populate their cell bodies surrounding to and distribute their dendrites in distinct but overlapping patterns within the primary olfactory center of the brain, the antennal lobe (AL). However, it remains unclear whether the same molecular mechanisms are employed to generate the appropriate dendritic patterns in discrete AL glomeruli among PNs produced from different neuroblasts. Here, by examining a previously explored transmembrane protein Semaphorin-1a (Sema-1a) which was proposed to globally control initial PN dendritic targeting along the dorsolateral-to-ventromedial axis of the AL, we discover a new role for Sema-1a in preventing dendrites of both uni-glomerular and poly-glomerular PNs from aberrant invasion into select AL regions and, intriguingly, this Sema-1a-deficient dendritic mis-targeting phenotype seems to associate with the origins of PNs from which they are derived. Further, ectopic expression of Sema-1a resulted in PN dendritic mis-projection from a select AL region into adjacent glomeruli, strengthening the idea that Sema-1a plays an essential role in preventing abnormal dendritic accumulation in select AL regions. Taken together, these results demonstrate that Sema-1a repulsion keeps dendrites of different types of PNs away from each other, enabling the same types of PN dendrites to be sorted into destined AL glomeruli and permitting for functional assembly of olfactory circuitry.
阐明嗅觉系统神经元中如何形成合适的神经突模式对于理解嗅觉图谱的构建至关重要。在果蝇嗅觉系统中,投射神经元(PNs)主要来源于四个神经干细胞(称为神经母细胞),其细胞体聚集在大脑的主要嗅觉中心触角叶(AL)周围,并以独特但重叠的模式分布其树突。然而,尚不清楚在由不同神经母细胞产生的PNs中,是否采用相同的分子机制在离散的AL肾小球中产生合适的树突模式。在这里,通过研究一种先前探索过的跨膜蛋白信号素-1a(Sema-1a),该蛋白被认为可沿AL的背外侧到腹内侧轴全局控制PN树突的初始靶向,我们发现Sema-1a在防止单肾小球和多肾小球PNs的树突异常侵入特定AL区域方面具有新作用,有趣的是,这种Sema-1a缺陷型树突错误靶向表型似乎与它们所源自的PNs的起源有关。此外,Sema-1a的异位表达导致PN树突从特定的AL区域错误投射到相邻的肾小球,强化了Sema-1a在防止特定AL区域异常树突积累中起重要作用的观点。综上所述,这些结果表明Sema-1a的排斥作用使不同类型的PNs树突彼此分开,使相同类型的PNs树突能够被分类到预定的AL肾小球中,并允许嗅觉回路进行功能组装。