Hige Toshihide, Aso Yoshinori, Rubin Gerald M, Turner Glenn C
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.
Janelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, Virginia 20147, USA.
Nature. 2015 Oct 8;526(7572):258-62. doi: 10.1038/nature15396. Epub 2015 Sep 30.
Although all sensory circuits ascend to higher brain areas where stimuli are represented in sparse, stimulus-specific activity patterns, relatively little is known about sensory coding on the descending side of neural circuits, as a network converges. In insects, mushroom bodies have been an important model system for studying sparse coding in the olfactory system, where this format is important for accurate memory formation. In Drosophila, it has recently been shown that the 2,000 Kenyon cells of the mushroom body converge onto a population of only 34 mushroom body output neurons (MBONs), which fall into 21 anatomically distinct cell types. Here we provide the first, to our knowledge, comprehensive view of olfactory representations at the fourth layer of the circuit, where we find a clear transition in the principles of sensory coding. We show that MBON tuning curves are highly correlated with one another. This is in sharp contrast to the process of progressive decorrelation of tuning in the earlier layers of the circuit. Instead, at the population level, odour representations are reformatted so that positive and negative correlations arise between representations of different odours. At the single-cell level, we show that uniquely identifiable MBONs display profoundly different tuning across different animals, but that tuning of the same neuron across the two hemispheres of an individual fly was nearly identical. Thus, individualized coordination of tuning arises at this level of the olfactory circuit. Furthermore, we find that this individualization is an active process that requires a learning-related gene, rutabaga. Ultimately, neural circuits have to flexibly map highly stimulus-specific information in sparse layers onto a limited number of different motor outputs. The reformatting of sensory representations we observe here may mark the beginning of this sensory-motor transition in the olfactory system.
尽管所有感觉回路都会上升到更高的脑区,在那里刺激以稀疏的、特定于刺激的活动模式来呈现,但对于神经回路下行侧(即网络汇聚处)的感觉编码却知之甚少。在昆虫中,蘑菇体一直是研究嗅觉系统中稀疏编码的重要模型系统,这种编码形式对于准确的记忆形成至关重要。在果蝇中,最近的研究表明,蘑菇体的2000个肯扬细胞汇聚到仅34个蘑菇体输出神经元(MBON)组成的群体上,这些神经元可分为21种解剖学上不同的细胞类型。在此,据我们所知,我们首次提供了该回路第四层嗅觉表征的全面视图,我们发现感觉编码原则在此处有明显转变。我们表明,MBON的调谐曲线彼此高度相关。这与回路早期层中调谐逐渐去相关的过程形成鲜明对比。相反,在群体水平上,气味表征被重新格式化,以便不同气味的表征之间产生正相关和负相关。在单细胞水平上,我们表明,唯一可识别的MBON在不同动物之间表现出截然不同的调谐,但单个果蝇两个半球中同一神经元的调谐几乎相同。因此,调谐的个性化协调出现在嗅觉回路的这一层次。此外,我们发现这种个性化是一个活跃的过程,需要一个与学习相关的基因——芜菁甘蓝基因。最终,神经回路必须将稀疏层中高度特定于刺激的信息灵活地映射到有限数量的不同运动输出上。我们在此观察到的感觉表征的重新格式化可能标志着嗅觉系统中这种感觉-运动转换的开始。