3R Computer-Based Modelling, Faculty of Medicine, ICAR3R, Justus Liebig University Giessen, Giessen, Germany.
Ernst Strüngmann Institute (ESI) for Neuroscience in cooperation with the Max Planck Society, Frankfurt am Main, Germany.
PLoS Comput Biol. 2024 Feb 23;20(2):e1011267. doi: 10.1371/journal.pcbi.1011267. eCollection 2024 Feb.
Investigating and modelling the functionality of human neurons remains challenging due to the technical limitations, resulting in scarce and incomplete 3D anatomical reconstructions. Here we used a morphological modelling approach based on optimal wiring to repair the parts of a dendritic morphology that were lost due to incomplete tissue samples. In Drosophila, where dendritic regrowth has been studied experimentally using laser ablation, we found that modelling the regrowth reproduced a bimodal distribution between regeneration of cut branches and invasion by neighbouring branches. Interestingly, our repair model followed growth rules similar to those for the generation of a new dendritic tree. To generalise the repair algorithm from Drosophila to mammalian neurons, we artificially sectioned reconstructed dendrites from mouse and human hippocampal pyramidal cell morphologies, and showed that the regrown dendrites were morphologically similar to the original ones. Furthermore, we were able to restore their electrophysiological functionality, as evidenced by the recovery of their firing behaviour. Importantly, we show that such repairs also apply to other neuron types including hippocampal granule cells and cerebellar Purkinje cells. We then extrapolated the repair to incomplete human CA1 pyramidal neurons, where the anatomical boundaries of the particular brain areas innervated by the neurons in question were known. Interestingly, the repair of incomplete human dendrites helped to simulate the recently observed increased synaptic thresholds for dendritic NMDA spikes in human versus mouse dendrites. To make the repair tool available to the neuroscience community, we have developed an intuitive and simple graphical user interface (GUI), which is available in the TREES toolbox (www.treestoolbox.org).
由于技术限制,研究和模拟人类神经元的功能仍然具有挑战性,导致 3D 解剖重建稀缺且不完整。在这里,我们使用了一种基于最优布线的形态建模方法来修复由于组织样本不完整而丢失的树突形态部分。在果蝇中,已经使用激光消融实验研究了树突的再生,我们发现,对再生进行建模可以再现切割分支的再生和相邻分支的入侵之间的双峰分布。有趣的是,我们的修复模型遵循的生长规则与新树突生成的规则相似。为了将修复算法从果蝇推广到哺乳动物神经元,我们人为地对来自小鼠和人类海马锥体神经元形态的重建树突进行了切片,并表明再生的树突在形态上与原始树突相似。此外,我们还能够恢复其电生理功能,这可以从它们的放电行为恢复得到证明。重要的是,我们表明这种修复方法也适用于其他神经元类型,包括海马颗粒细胞和小脑浦肯野细胞。然后,我们将修复方法外推到不完整的人类 CA1 锥体神经元,这些神经元的解剖边界已知。有趣的是,对不完整的人类树突进行修复有助于模拟最近观察到的人类与小鼠树突中树突 NMDA 峰的突触阈值增加。为了将修复工具提供给神经科学界,我们开发了一个直观而简单的图形用户界面 (GUI),可在 TREES 工具箱(www.treestoolbox.org)中使用。