Deep convolutional neural networks for segmenting 3D in vivo multiphoton images of vasculature in Alzheimer disease mouse models

被引:53
作者
Haft-Javaherian, Mohammad [1 ]
Fang, Linjing [1 ]
Muse, Victorine [1 ]
Schaffer, Chris B. [1 ]
Nishimura, Nozomi [1 ]
Sabuncu, Mert R. [1 ,2 ]
机构
[1] Cornell Univ, Nancy E & Peter C Meinig Sch Biomed Engn, Ithaca, NY 14850 USA
[2] Cornell Univ, Sch Elect & Comp Engn, Ithaca, NY 14850 USA
基金
美国国家科学基金会; 欧洲研究理事会; 美国国家卫生研究院;
关键词
2-PHOTON MICROSCOPY; BLOOD-FLOW; BRAIN; CORTEX; ARCHITECTURE; CAPILLARIES; ALGORITHM; TERM; TOOL;
D O I
10.1371/journal.pone.0213539
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The health and function of tissue rely on its vasculature network to provide reliable blood perfusion. Volumetric imaging approaches, such as multiphoton microscopy, are able to generate detailed 3D images of blood vessels that could contribute to our understanding of the role of vascular structure in normal physiology and in disease mechanisms. The segmentation of vessels, a core image analysis problem, is a bottleneck that has prevented the systematic comparison of 3D vascular architecture across experimental populations. We explored the use of convolutional neural networks to segment 3D vessels within volumetric in vivo images acquired by multiphoton microscopy. We evaluated different network architectures and machine learning techniques in the context of this segmentation problem. We show that our optimized convolutional neural network architecture with a customized loss function, which we call DeepVess, yielded a segmentation accuracy that was better than state-of-the-art methods, while also being orders of magnitude faster than the manual annotation. To explore the effects of aging and Alzheimer's disease on capillaries, we applied DeepVess to 3D images of cortical blood vessels in young and old mouse models of Alzheimer's disease and wild type littermates. We found little difference in the distribution of capillary diameter or tortuosity between these groups, but did note a decrease in the number of longer capillary segments (>75 mu m) in aged animals as compared to young, in both wild type and Alzheimer's disease mouse models.
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页数:21
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