Inglis A, Cruz L, Roe D L, Stanley H E, Rosene D L, Urbanc B
Center for Polymer Studies, Department of Physics, Boston University, Boston, MA 02215, USA.
J Microsc. 2008 Jun;230(Pt 3):339-52. doi: 10.1111/j.1365-2818.2008.01992.x.
Individual locations of many neuronal cell bodies (>10(4)) are needed to enable statistically significant measurements of spatial organization within the brain such as nearest-neighbour and microcolumnarity measurements. In this paper, we introduce an Automated Neuron Recognition Algorithm (ANRA) which obtains the (x, y) location of individual neurons within digitized images of Nissl-stained, 30 microm thick, frozen sections of the cerebral cortex of the Rhesus monkey. Identification of neurons within such Nissl-stained sections is inherently difficult due to the variability in neuron staining, the overlap of neurons, the presence of partial or damaged neurons at tissue surfaces, and the presence of non-neuron objects, such as glial cells, blood vessels, and random artefacts. To overcome these challenges and identify neurons, ANRA applies a combination of image segmentation and machine learning. The steps involve active contour segmentation to find outlines of potential neuron cell bodies followed by artificial neural network training using the segmentation properties (size, optical density, gyration, etc.) to distinguish between neuron and non-neuron segmentations. ANRA positively identifies 86 +/- 5% neurons with 15 +/- 8% error (mean +/- SD) on a wide range of Nissl-stained images, whereas semi-automatic methods obtain 80 +/- 7%/17 +/- 12%. A further advantage of ANRA is that it affords an unlimited increase in speed from semi-automatic methods, and is computationally efficient, with the ability to recognize approximately 100 neurons per minute using a standard personal computer. ANRA is amenable to analysis of huge photo-montages of Nissl-stained tissue, thereby opening the door to fast, efficient and quantitative analysis of vast stores of archival material that exist in laboratories and research collections around the world.
为了能够对大脑内的空间组织进行具有统计学意义的测量,例如最近邻和微柱性测量,需要许多神经元细胞体(>10⁴)的个体位置。在本文中,我们介绍了一种自动神经元识别算法(ANRA),该算法可在恒河猴大脑皮层尼氏染色、30微米厚的冷冻切片数字化图像中获取单个神经元的(x, y)位置。由于神经元染色的变异性、神经元的重叠、组织表面存在部分或受损神经元以及存在非神经元物体(如神经胶质细胞、血管和随机伪像),在这种尼氏染色切片中识别神经元本身就很困难。为了克服这些挑战并识别神经元,ANRA应用了图像分割和机器学习的组合。步骤包括主动轮廓分割以找到潜在神经元细胞体的轮廓,然后使用分割属性(大小、光密度、回转等)进行人工神经网络训练,以区分神经元和非神经元分割。在各种尼氏染色图像上,ANRA能正确识别86±5%的神经元,误差为15±8%(平均值±标准差),而半自动方法的识别率为80±7%/17±12%。ANRA的另一个优点是,与半自动方法相比,它的速度可以无限提高,并且计算效率高,使用标准个人计算机每分钟能够识别大约100个神经元。ANRA适用于对尼氏染色组织的巨大照片蒙太奇进行分析,从而为快速、高效和定量分析世界各地实验室和研究收藏中存在的大量档案材料打开了大门。