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全脑哺乳动物连接组学成像方法的比较前景

Comparative prospects of imaging methods for whole-brain mammalian connectomics.

作者信息

Collins Logan Thrasher, Huffman Todd, Koene Randal

机构信息

Washington University in St. Louis, Department of Biomedical Engineering, St. Louis, MO, USA.

E11 Bio, Alameda, CA, USA.

出版信息

Cell Rep Methods. 2025 Feb 24;5(2):100988. doi: 10.1016/j.crmeth.2025.100988. Epub 2025 Feb 18.

Abstract

Mammalian whole-brain connectomes are a foundational ingredient for a holistic understanding of brains. Indeed, imaging connectomes at sufficient resolution to densely reconstruct cellular morphology and synapses represents a long-standing goal in neuroscience. Mouse connectomes could soon come within reach, while human connectomes remain a more distant yet still worthy goal. Though the technologies needed to reconstruct whole-brain connectomes have not yet reached full maturity, they are advancing rapidly. Close examination of these technologies may help plan connectomics projects. Here, we quantitatively compare imaging technologies that have the potential to enable whole-brain mammalian connectomics. We perform calculations on electron microscopy (EM) techniques and expansion light-sheet fluorescence microscopy (ExLSFM) methods. We consider techniques that have sufficient resolution to identify all synapses and sufficient speed to be relevant for whole mammalian brains. We offer this analysis as a resource for those considering how to organize efforts toward imaging whole-brain mammalian connectomes.

摘要

哺乳动物全脑连接组是全面理解大脑的基础要素。事实上,以足够的分辨率对连接组进行成像以密集重建细胞形态和突触是神经科学的一个长期目标。小鼠连接组可能很快就能实现,而人类连接组仍然是一个更遥远但仍有价值的目标。尽管重建全脑连接组所需的技术尚未完全成熟,但它们正在迅速发展。仔细研究这些技术可能有助于规划连接组学项目。在这里,我们定量比较了有可能实现全脑哺乳动物连接组学的成像技术。我们对电子显微镜(EM)技术和扩展光片荧光显微镜(ExLSFM)方法进行了计算。我们考虑的技术要有足够的分辨率来识别所有突触,并且要有足够的速度来适用于整个哺乳动物大脑。我们提供此分析作为一种资源,供那些考虑如何组织力量对全脑哺乳动物连接组进行成像的人参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491c/11955263/6c80c122b34c/gr1.jpg

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