Li Qiufu, Zhang Yu, Liang Hanbang, Gong Hui, Jiang Liang, Liu Qiong, Shen Linlin
Computer Vision Institute, College of Computer Science and Software Engineering, Shenzhen University, Shenzhen, Guangdong, 518060, China; AI Research Center for Medical Image Analysis and Diagnosis, Shenzhen University, Shenzhen 518060, China; Guangdong Key Laboratory of Intelligent Information Processing, Shenzhen University, Shenzhen 518060, China.
College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, Guangdong, 518055, China.
Comput Methods Programs Biomed. 2021 May;203:106023. doi: 10.1016/j.cmpb.2021.106023. Epub 2021 Mar 10.
Alzheimer's Disease (AD) is associated with neuronal damage and decrease. Micro-Optical Sectioning Tomography (MOST) provides an approach to acquire high-resolution images for neuron analysis in the whole-brain. Application of this technique to AD mouse brain enables us to investigate neuron changes during the progression of AD pathology. However, how to deal with the huge amount of data becomes the bottleneck.
Using MOST technology, we acquired 3D whole-brain images of six AD mice, and sampled the imaging data of four regions in each mouse brain for AD progression analysis. To count the number of neurons, we proposed a deep learning based method by detecting neuronal soma in the neuronal images. In our method, the neuronal images were first cut into small cubes, then a Convolutional Neural Network (CNN) classifier was designed to detect the neuronal soma by classifying the cubes into three categories, "soma", "fiber", and "background".
Compared with the manual method and currently available NeuroGPS software, our method demonstrates faster speed and higher accuracy in identifying neurons from the MOST images. By applying our method to various brain regions of 6-month-old and 12-month-old AD mice, we found that the amount of neurons in three brain regions (lateral entorhinal cortex, medial entorhinal cortex, and presubiculum) decreased slightly with the increase of age, which is consistent with the experimental results previously reported.
This paper provides a new method to automatically handle the huge amounts of data and accurately identify neuronal soma from the MOST images. It also provides the potential possibility to construct a whole-brain neuron projection to reveal the impact of AD pathology on mouse brain.
阿尔茨海默病(AD)与神经元损伤和减少有关。显微光学切片断层成像(MOST)提供了一种获取全脑神经元分析高分辨率图像的方法。将该技术应用于AD小鼠脑,使我们能够研究AD病理进展过程中的神经元变化。然而,如何处理大量数据成为了瓶颈。
利用MOST技术,我们获取了6只AD小鼠的三维全脑图像,并对每只小鼠脑内4个区域的成像数据进行采样以进行AD进展分析。为了计算神经元数量,我们提出了一种基于深度学习的方法,通过在神经元图像中检测神经元胞体来实现。在我们的方法中,首先将神经元图像切成小立方体,然后设计一个卷积神经网络(CNN)分类器,通过将立方体分为“胞体”、“纤维”和“背景”三类来检测神经元胞体。
与手动方法和现有的NeuroGPS软件相比,我们的方法在从MOST图像中识别神经元方面具有更快的速度和更高的准确性。通过将我们的方法应用于6个月和12个月大的AD小鼠的不同脑区,我们发现三个脑区(外侧内嗅皮质、内侧内嗅皮质和前扣带回)的神经元数量随年龄增长略有减少,这与先前报道的实验结果一致。
本文提供了一种自动处理大量数据并从MOST图像中准确识别神经元胞体的新方法。它还提供了构建全脑神经元投影以揭示AD病理对小鼠脑影响的潜在可能性。