Physics Department, University of Oregon, Eugene, OR, 97403, USA.
School of Pharmacy, University of Auckland, Auckland, 1142, New Zealand.
Sci Rep. 2021 Jan 27;11(1):2332. doi: 10.1038/s41598-021-81421-2.
We investigate the degree to which neurons are fractal, the origin of this fractality, and its impact on functionality. By analyzing three-dimensional images of rat neurons, we show the way their dendrites fork and weave through space is unexpectedly important for generating fractal-like behavior well-described by an 'effective' fractal dimension D. This discovery motivated us to create distorted neuron models by modifying the dendritic patterns, so generating neurons across wide ranges of D extending beyond their natural values. By charting the D-dependent variations in inter-neuron connectivity along with the associated costs, we propose that their D values reflect a network cooperation that optimizes these constraints. We discuss the implications for healthy and pathological neurons, and for connecting neurons to medical implants. Our automated approach also facilitates insights relating form and function, applicable to individual neurons and their networks, providing a crucial tool for addressing massive data collection projects (e.g. connectomes).
我们研究神经元的分形程度、这种分形的起源及其对功能的影响。通过分析大鼠神经元的三维图像,我们展示了树突分叉和在空间中交织的方式对于产生分形样行为非常重要,这种行为可以用一个“有效”分形维数 D 很好地描述。这一发现促使我们通过改变树突模式来创建扭曲的神经元模型,从而生成具有广泛 D 值范围的神经元,超出其自然值。通过绘制沿 D 变化的神经元间连接的变化以及相关成本,我们提出它们的 D 值反映了一种网络合作,这种合作优化了这些约束。我们讨论了对健康和病态神经元以及将神经元与医学植入物连接的影响。我们的自动化方法还促进了形态和功能之间的深入了解,适用于单个神经元及其网络,为处理大规模数据收集项目(例如连接组学)提供了一个关键工具。