A comparison of manual neuronal reconstruction from biocytin histology or 2-photon imaging: morphometry and computer modeling

被引:17
作者
Blackman, Arne V. [1 ]
Grabuschnig, Stefan [2 ]
Legenstein, Robert [2 ]
Sjoestroem, P. Jesper [1 ,3 ]
机构
[1] UCL, Dept Neurosci Physiol & Pharmacol, London, England
[2] Graz Univ Technol, Inst Theoret Comp Sci, A-8010 Graz, Austria
[3] McGill Univ, Dept Neurol & Neurosurg, Montreal Gen Hosp, Ctr Res Neurosci,Res Inst,Hlth Ctr, Montreal, PQ H3G 1A4, Canada
来源
FRONTIERS IN NEUROANATOMY | 2014年 / 8卷
基金
英国生物技术与生命科学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
morphology; reconstruction; cell-type classification; multicompartmental modeling; interneurons; 2-photon imaging; Neurolucida; neocortex; DIGITAL RECONSTRUCTIONS; COINCIDENCE DETECTION; PYRAMIDAL NEURONS; DENDRITIC SPINES; GRANULE CELLS; CHALLENGES; MORPHOLOGY; CLASSIFICATION; INTERNEURONS; NOMENCLATURE;
D O I
10.3389/fnana.2014.00065
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Accurate 3D reconstruction of neurons is vital for applications linking anatomy and physiology. Reconstructions are typically created using Neurolucida after biocytin histology (BH). An alternative inexpensive and fast method is to use freeware such as Neuromantic to reconstruct from fluorescence imaging (El) stacks acquired using 2-photon laser-scanning microscopy during physiological recording. We compare these two methods with respect to morphometry, cell classification, and multicompartmental modeling in the NEURON simulation environment. Quantitative morphological analysis of the same cells reconstructed using both methods reveals that whilst biocytin reconstructions facilitate tracing of more distal collaterals, both methods are comparable in representing the overall morphology: automated clustering of reconstructions from both methods successfully separates neocortical basket cells from pyramidal cells but not BH from Fl reconstructions. BH reconstructions suffer more from tissue shrinkage and compression artifacts than Fl reconstructions do. Fl reconstructions, on the other hand, consistently have larger process diameters. Consequently, significant differences in NEURON modeling of excitatory post-synaptic potential (EPSP) forward propagation are seen between the two methods, with Fl reconstructions exhibiting smaller depolarizations. Simulated action potential backpropagation (bAP), however, is indistinguishable between reconstructions obtained with the two methods. In our hands, BH reconstructions are necessary for NEURON modeling and detailed morphological tracing, and thus remain state of the art, although they are more labor intensive, more expensive, and suffer from a higher failure rate due to the occasional poor outcome of histological processing. However, for a subset of anatomical applications such as cell type identification, Fl reconstructions are superior, because of indistinguishable classification performance with greater ease of use, essentially 100% success rate, and lower cost.
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页数:13
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