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抑制胆碱能投射神经元中的氧化应激可完全挽救. 与衰老相关的嗅觉回路退化。

Inhibition of oxidative stress in cholinergic projection neurons fully rescues aging-associated olfactory circuit degeneration in .

机构信息

TUM School of Life Sciences, Technical University of Munich, Freising, Germany.

Institute of Biology, Free University of Berlin, Neurogenetics, Germany.

出版信息

Elife. 2018 Jan 18;7:e32018. doi: 10.7554/eLife.32018.

Abstract

Loss of the sense of smell is among the first signs of natural aging and neurodegenerative diseases such as Alzheimer's and Parkinson's. Cellular and molecular mechanisms promoting this smell loss are not understood. Here, we show that also loses olfaction before vision with age. Within the olfactory circuit, cholinergic projection neurons show a reduced odor response accompanied by a defect in axonal integrity and reduction in synaptic marker proteins. Using behavioral functional screening, we pinpoint that expression of the mitochondrial reactive oxygen scavenger SOD2 in cholinergic projection neurons is necessary and sufficient to prevent smell degeneration in aging flies. Together, our data suggest that oxidative stress induced axonal degeneration in a single class of neurons drives the functional decline of an entire neural network and the behavior it controls. Given the important role of the cholinergic system in neurodegeneration, the fly olfactory system could be a useful model for the identification of drug targets.

摘要

嗅觉丧失是自然衰老和神经退行性疾病(如阿尔茨海默病和帕金森病)的最早迹象之一。促进这种嗅觉丧失的细胞和分子机制尚不清楚。在这里,我们表明 也随着年龄的增长而在视力丧失之前失去嗅觉。在嗅觉回路中,胆碱能投射神经元对气味的反应减弱,伴随着轴突完整性缺陷和突触标记蛋白减少。通过行为功能筛选,我们发现胆碱能投射神经元中线粒体活性氧清除剂 SOD2 的表达对于防止衰老果蝇的嗅觉退化是必要且充分的。总的来说,我们的数据表明,单个神经元类别的氧化应激诱导的轴突退化驱动整个神经网络及其控制的行为的功能下降。鉴于胆碱能系统在神经退行性变中的重要作用,果蝇嗅觉系统可能是鉴定药物靶点的有用模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2f7/5790380/32d67dc7b5de/elife-32018-fig1.jpg

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