研究果蝇嗅觉回路结构变化如何影响学习能力
The Impact of Structural Changes on Learning Capacity in the Fly Olfactory Neural Circuit
- 构建包含神经元连接的模型,模拟嗅觉学习过程
- 成熟肯扬细胞缺失使输出神经元分类错误率显著上升
- 结果对理解记忆机制和人工智能有启发意义
果蝇蘑菇体(MB)参与嗅觉学习与记忆,肯扬细胞(KC)到蘑菇体输出神经元(MBON)的突触可塑性在学习中起关键作用。以往研究集中于前馈神经元(PN)到肯扬细胞(KC)的连接,本文则关注KC到MBON回路结构改变对MBON区分不同气味类别能力的影响。我们构建了一个包含PN、KC和MBON连接的神经网络模型,生成十类人工输入以模拟不同气味引起的前馈神经元活动。通过测量KC-MBON连接数量、MBON错误率及突触权重等指标发现,具有较少前突触KC的MBON在气味分类任务中表现更差。发育成熟的KC类型对每个MBON的输出有显著影响。随机与靶向切除实验显示,去除发育成熟的KC比未成熟细胞对MBON学习能力的损害更大。随机与靶向修剪突触连接的结果与此一致。此外,我们在PN-KC回路中进行重连实验,进一步揭示了不同类型KC的作用。本研究深化了对嗅觉神经可塑性的理解,为学习与记忆机制提供了新线索,并对人工智能和神经退行性疾病治疗具潜在应用价值。
原文摘要 · Abstract (English)
The Drosophila mushroom body (MB) is known to be involved in olfactory learning and memory; the synaptic plasticity of the Kenyon cell (KC) to mushroom body output neuron (MBON) synapses plays a key role in the learning process. Previous research has focused on projection neuron (PN) to Kenyon cell (KC) connectivity within the MB; we examine how perturbations to the mushroom body circuit structure and changes in connectivity, specifically within the KC to mushroom body output neuron (MBON) neural circuit, affect the MBONs' ability to distinguish between odor classes. We constructed a neural network that incorporates the connectivity between PNs, KCs, and MBONs. To train our model, we generated ten artificial input classes, which represent the projection neuron activity in response to different odors. We collected data on the number of KC-to-MBON connections, MBON error rates, and KC-to-MBON synaptic weights, among other metrics. We observed that MBONs with very few presynaptic KCs consistently performed worse than others in the odor classification task. The developmental types of KCs also played a significant role in each MBON's output. We performed random and targeted KC ablation and observed that ablating developmentally mature KCs had a greater negative impact on MBONs' learning capacity than ablating immature KCs. Random and targeted pruning of KC-MBON synaptic connections yielded results largely consistent with the ablation experiments. To further explore the various types of KCs, we also performed rewiring experiments in the PN to KC circuit. Our study furthers our understanding of olfactory neuroplasticity and provides important clues to understanding learning and memory in general. Understanding how the olfactory circuits process and learn can also have potential applications in artificial intelligence and treatments for neurodegenerative diseases.
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