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3D reconstruction of 2D fluorescence histology images and registration with in vivo MR images: Application in a rodent stroke model

机译:2D荧光组织学图像的3D重建并与体内MR图像配准:在啮齿动物中风模型中的应用

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摘要

To validate and add value to non-invasive imaging techniques, the corresponding histology is required to establish biological correlates. We present an efficient, semi-automated image-processing pipeline that uses immunohistochemically stained sections to reconstruct a 3D brain volume from 2D histological images before registering these with the corresponding 3D in vivo magnetic resonance images (MRI). A multistep registration procedure that first aligns the "global" volume by using the centre of mass and then applies a rigid and affine alignment based on signal intensities is described. This technique was applied to a training set of three rat brain volumes before being validated on three normal brains. Application of the approach to register "abnormal" images from a rat model of stroke allowed the neurobiological correlates of the variations in the hyper-intense MRI signal intensity caused by infarction to be investigated. For evaluation, the corresponding anatomical landmarks in MR and histology were defined to measure the registration accuracy. A registration error of 0.249. mm (approximately one in-plane voxel dimension) was evident in healthy rat brains and of 0.323. mm in a rodent model of stroke. The proposed reconstruction and registration pipeline allowed for the precise analysis of non-invasive MRI and corresponding microstructural histological features in 3D. We were thus able to interrogate histology to deduce the cause of MRI signal variations in the lesion cavity and the peri-infarct area.
机译:为了验证非侵入性成像技术并为其增值,需要相应的组织学来建立生物学相关性。我们提出了一个高效,半自动化的图像处理管道,该管道使用免疫组织化学染色的切片从2D组织学图像重建3D脑体积,然后将其与相应的3D体内磁共振图像(MRI)进行配准。描述了一种多步配准过程,该过程首先通过使用质心对齐“全局”体积,然后基于信号强度进行刚性和仿射对齐。在对三个正常大脑进行验证之前,将该技术应用于三个大鼠大脑体积的训练集。应用该方法来注册来自中风大鼠模型的“异常”图像,可以研究由梗死引起的高强度MRI信号强度变化的神经生物学相关性。为了进行评估,在MR和组织学中定义了相应的解剖标志,以测量配准的准确性。注册错误为0.249。在健康大鼠的大脑中,毫米(约一个平面内体素尺寸)很明显,为0.323。在啮齿动物的中风模型中为mm。拟议的重建和配准管道可以精确分析3D非侵入性MRI和相应的显微组织学特征。因此,我们能够询问组织学,以推断病变腔和梗塞周围区域MRI信号变化的原因。

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