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StainAI:染色小胶质细胞的定量映射以及对心脏骤停时全脑神经炎症和治疗效果的见解

StainAI: quantitative mapping of stained microglia and insights into brain-wide neuroinflammation and therapeutic effects in cardiac arrest.

作者信息

Hsu Chao-Hsiung, Hsu Yi-Yu, Chang Be-Ming, Raffensperger Katherine, Kadden Micah, Ton Hoai T, Ette Essiet-Adidiong, Lin Stephen, Brooks Janiya, Burke Mark W, Lee Yih-Jing, Wang Paul C, Shoykhet Michael, Tu Tsang-Wei

机构信息

Molecular Imaging Laboratory, Department of Radiology, Howard University, Washington, DC, USA.

Miin Wu School of Computing, National Cheng Kung University, Tainan City, Taiwan.

出版信息

Commun Biol. 2025 Mar 20;8(1):462. doi: 10.1038/s42003-025-07926-y.

DOI:10.1038/s42003-025-07926-y
PMID:40114030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11926354/
Abstract

Microglia, the brain's resident macrophages, participate in development and influence neuroinflammation, which is characteristic of multiple brain pathologies. Diverse insults cause microglia to alter their morphology from "resting" to "activated" shapes, which vary with stimulus type, brain location, and microenvironment. This morphologic diversity commonly restricts microglial analyses to specific regions and manual methods. We introduce StainAI, a deep learning tool that leverages 20x whole-slide immunohistochemistry images for rapid, high-throughput analysis of microglial morphology. StainAI maps microglia to a brain atlas, classifies their morphology, quantifies morphometric features, and computes an activation score for any region of interest. As a proof of principle, StainAI was applied to a rat model of pediatric asphyxial cardiac arrest, accurately classifying millions of microglia across multiple slices, surpassing current methods by orders of magnitude, and identifying both known and novel activation patterns. Extending its application to a non-human primate model of simian immunodeficiency virus infection further demonstrated its generalizability beyond rodent datasets, providing new insights into microglial responses across species. StainAI offers a scalable, high-throughput solution for microglial analysis from routine immunohistochemistry images, accelerating research in microglial biology and neuroinflammation.

摘要

小胶质细胞是大脑中的常驻巨噬细胞,参与大脑发育并影响神经炎症,而神经炎症是多种脑部疾病的特征。多种损伤会导致小胶质细胞的形态从“静止”变为“活化”,其形态会因刺激类型、脑区位置和微环境而异。这种形态多样性通常将小胶质细胞的分析限制在特定区域和手动方法上。我们引入了StainAI,这是一种深度学习工具,它利用20倍全切片免疫组化图像对小胶质细胞形态进行快速、高通量分析。StainAI将小胶质细胞映射到脑图谱,对其形态进行分类,量化形态特征,并为任何感兴趣区域计算激活分数。作为原理验证,StainAI应用于小儿窒息性心脏骤停大鼠模型,准确地对多个切片中的数百万个小胶质细胞进行分类,比现有方法在数量级上有显著提升,并识别出已知和新的激活模式。将其应用扩展到猿猴免疫缺陷病毒感染的非人灵长类动物模型,进一步证明了其在啮齿动物数据集之外的通用性,为跨物种的小胶质细胞反应提供了新的见解。StainAI为从常规免疫组化图像进行小胶质细胞分析提供了一种可扩展的高通量解决方案,加速了小胶质细胞生物学和神经炎症方面的研究。

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本文引用的文献

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A single-cell atlas deconstructs heterogeneity across multiple models in murine traumatic brain injury and identifies novel cell-specific targets.单细胞图谱解析了小鼠创伤性脑损伤中多个模型的异质性,并确定了新的细胞特异性靶点。
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