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LungVis 1.0:一个自动的人工智能驱动的 3D 成像生态系统,揭示了纳米颗粒传递的空间分布和肺巨噬细胞的肺泡迁移。

LungVis 1.0: an automatic AI-powered 3D imaging ecosystem unveils spatial profiling of nanoparticle delivery and acinar migration of lung macrophages.

机构信息

Institute of Lung Health and Immunity (LHI), Helmholtz Munich, Comprehensive Pneumology Center (CPC-M), Member of the German Center for Lung Research (DZL), Munich, Germany.

Department of Thoracic Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Nat Commun. 2024 Nov 27;15(1):10138. doi: 10.1038/s41467-024-54267-1.

Abstract

Targeted (nano-)drug delivery is essential for treating respiratory diseases, which are often confined to distinct lung regions. However, spatio-temporal profiling of drugs or nanoparticles (NPs) and their interactions with lung macrophages remains unresolved. Here, we present LungVis 1.0, an AI-powered imaging ecosystem that integrates light sheet fluorescence microscopy with deep learning-based image analysis pipelines to map NP deposition and dosage holistically and quantitatively across bronchial and alveolar (acinar) regions in murine lungs for widely-used bulk-liquid and aerosol-based delivery methods. We demonstrate that bulk-liquid delivery results in patchy NP distribution with elevated bronchial doses, whereas aerosols achieve uniform deposition reaching distal alveoli. Furthermore, we reveal that lung tissue-resident macrophages (TRMs) are dynamic, actively patrolling and redistributing NPs within alveoli, contesting the conventional paradigm of TRMs as static entities. LungVis 1.0 provides an advanced framework for exploring pulmonary delivery dynamics and deepening insights into TRM-mediated lung immunity.

摘要

靶向(纳米)药物递送对于治疗呼吸系统疾病至关重要,因为这些疾病通常局限于特定的肺部区域。然而,药物或纳米颗粒(NPs)的时空分布及其与肺巨噬细胞的相互作用仍未得到解决。在这里,我们展示了 LungVis 1.0,这是一个由人工智能驱动的成像生态系统,它将光片荧光显微镜与基于深度学习的图像分析管道相结合,以全面和定量地绘制 NP 在支气管和肺泡(腺泡)区域的沉积和剂量,适用于广泛使用的批量液体和基于气溶胶的输送方法。我们证明,批量液体输送会导致 NP 分布不均匀,支气管剂量升高,而气溶胶则能实现均匀沉积,到达远端肺泡。此外,我们还揭示了肺组织驻留巨噬细胞(TRMs)是动态的,它们在肺泡内主动巡逻和重新分配 NPs,这与 TRMs 作为静态实体的传统观点相矛盾。LungVis 1.0 提供了一个先进的框架,用于探索肺部输送动力学,并深入了解 TRM 介导的肺部免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b752/11603200/105bdc4ba64e/41467_2024_54267_Fig1_HTML.jpg

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