Real-time single-particle imaging of functional lungs reveals mosaic-like patterns of aerosol deposition in alveoli.

IF 26.3 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Gabrielle N Grifno,Han Ali Kahvecioglu,Robert LeBourdais,Victoria Travnik,Rohin Banerji,Winita Wangsrikhun,Linzheng Shi,Suleyman B Bozal,Heewon Suh,Ahmed A Raslan,Athanasios Batgidis,Byungjun Kang,Feiyang Deng,Caleb Dalton,Andrew Tsao,Lauren Castle,Kathryn Regan,Abdulrahman Kobayter,Michael Vannini,Mohammad Rashidian,Liang Hao,Giovanni Ligresti,Joseph P Mizgerd,Worth Longest,Michael Hindle,W Mark Saltzman,James P Butler,Béla Suki,Hadi T Nia
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引用次数: 0

Abstract

Inhaled pathogens, pollutants and therapeutics interact with the dynamic architecture of the alveoli, yet how individual particles move and deposit at cellular resolution remains unclear. Here, utilizing the crystal ribcage platform, we track aerosol transport in ex vivo, actively ventilated lungs using real-time fluorescence imaging with single-particle resolution, capturing droplet trajectories, free-flight motion, impact orientation and deposition timescales within functional alveoli. These measurements show that intra-alveolar transport is directional and shaped by airway-guided flow and tissue motion. At larger scales, aerosols do not disperse uniformly throughout the lung's volume but instead concentrate into geometrically constrained clusters of alveoli, forming a conserved mosaic-like compartmentalization while neighbouring alveoli remain largely unexposed. The pattern persists across particle types and species and varies with particle properties and lung age. In models of emphysema, fibrosis and metastasis, airway remodelling alters both the geometry and amount of deposition. These multiscale insights reveal how single-particle transport and airway structure together shape alveolar exposure, immune activation, development and therapeutic accessibility.
功能肺的实时单颗粒成像显示肺泡内气溶胶沉积的马赛克样模式。
吸入的病原体、污染物和治疗药物与肺泡的动态结构相互作用,但个体颗粒如何在细胞分辨率上移动和沉积尚不清楚。在这里,利用晶体胸腔平台,我们利用单粒子分辨率实时荧光成像跟踪离体、主动通气肺中的气溶胶运输,捕捉功能肺泡内液滴轨迹、自由飞行运动、撞击方向和沉积时间尺度。这些测量表明,肺泡内运输是定向的,由气道引导的流动和组织运动形成。在更大的尺度上,气溶胶不是均匀地分散在肺内,而是集中在几何上受限的肺泡簇中,形成保守的马赛克状区隔,而邻近的肺泡基本上保持不暴露。这种模式在颗粒类型和物种中持续存在,并随颗粒性质和肺年龄而变化。在肺气肿、纤维化和转移模型中,气道重塑改变了沉积的几何形状和数量。这些多尺度的见解揭示了单颗粒运输和气道结构如何共同影响肺泡暴露、免疫激活、发育和治疗可及性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Biomedical Engineering
Nature Biomedical Engineering Medicine-Medicine (miscellaneous)
CiteScore
45.30
自引率
1.10%
发文量
138
期刊介绍: Nature Biomedical Engineering is an online-only monthly journal that was launched in January 2017. It aims to publish original research, reviews, and commentary focusing on applied biomedicine and health technology. The journal targets a diverse audience, including life scientists who are involved in developing experimental or computational systems and methods to enhance our understanding of human physiology. It also covers biomedical researchers and engineers who are engaged in designing or optimizing therapies, assays, devices, or procedures for diagnosing or treating diseases. Additionally, clinicians, who make use of research outputs to evaluate patient health or administer therapy in various clinical settings and healthcare contexts, are also part of the target audience.
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