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SMART: WholeBrain 的开源扩展,用于完整小鼠脑的注册和分割。

SMART: An Open-Source Extension of WholeBrain for Intact Mouse Brain Registration and Segmentation.

机构信息

Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore 21224, MD

Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore 21224, MD.

出版信息

eNeuro. 2022 May 3;9(3). doi: 10.1523/ENEURO.0482-21.2022. Print 2022 May-Jun.

Abstract

Mapping immediate early gene (IEG) expression across intact mouse brains allows for unbiased identification of brain-wide activity patterns underlying complex behaviors. Accurate registration of sample brains to a common anatomic reference is critical for precise assignment of IEG-positive ("active") neurons to known brain regions of interest (ROIs). While existing automated voxel-based registration methods provide a high-throughput solution, they require substantial computing power, can be difficult to implement and fail when brains are damaged or only partially imaged. Additionally, it is challenging to cross-validate these approaches or compare them to any preexisting literature based on serial coronal sectioning. Here, we present the open-source R package SMART (Semi-Manual Alignment to Reference Templates) that extends the WholeBrain R package framework to automated segmentation and semi-automated registration of intact mouse brain light-sheet fluorescence microscopy (LSFM) datasets. The SMART package was created for novice programmers and introduces a streamlined pipeline for aligning, registering, and segmenting LSFM volumetric datasets across the anterior-posterior (AP) axis, using a simple "choice game" and interactive menus. SMART provides the flexibility to register whole brains, partial brains or discrete user-chosen images, and is fully compatible with traditional sectioned coronal slice-based analyses. We demonstrate SMART's core functions using example datasets and provide step-by-step video tutorials for installation and implementation of the package. We also present a modified iDISCO+ tissue clearing procedure for uniform immunohistochemical labeling of the activity marker Fos across intact mouse brains. The SMART pipeline, in conjunction with the modified iDISCO+ Fos procedure, is ideally suited for examination and orthogonal cross-validation of brain-wide neuronal activation datasets.

摘要

在完整的小鼠大脑中绘制即时早期基因 (IEG) 的表达图谱,可以实现对复杂行为背后的全脑活动模式进行无偏识别。准确地将样本大脑注册到共同的解剖参考系对于将 IEG 阳性(“活跃”)神经元精确分配到已知的感兴趣脑区 (ROI) 至关重要。虽然现有的自动化体素配准方法提供了高通量的解决方案,但它们需要大量的计算能力,实施起来可能很困难,并且在大脑受损或仅部分成像时会失败。此外,交叉验证这些方法或将其与基于连续冠状切片的任何现有文献进行比较具有挑战性。在这里,我们提出了开源 R 包 SMART(参考模板的半自动对齐),它扩展了 WholeBrain R 包框架,以实现对完整小鼠脑光片荧光显微镜 (LSFM) 数据集的自动分割和半自动注册。SMART 包专为新手程序员创建,引入了一种简化的流水线,用于在前后 (AP) 轴上对齐、注册和分割 LSFM 体数据集,使用简单的“选择游戏”和交互式菜单。SMART 提供了注册整个大脑、部分大脑或用户选择的离散图像的灵活性,并且与传统的冠状切片基于分析完全兼容。我们使用示例数据集展示了 SMART 的核心功能,并提供了有关软件包安装和实施的分步视频教程。我们还提出了一种改良的 iDISCO+组织透明化程序,用于在完整的小鼠大脑中均匀标记活性标记物 Fos。SMART 流水线与改良的 iDISCO+Fos 程序相结合,非常适合检查和对全脑神经元激活数据集进行正交交叉验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b731/9070730/7c09a50796c5/ENEURO.0482-21.2022_f001.jpg

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