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时空建模量化了细胞对人类肺部烟曲霉摄取的贡献。

Spatiotemporal modeling quantifies cellular contributions to uptake of Aspergillus fumigatus in the human lung.

作者信息

Saffer Christoph, Timme Sandra, Ortiz Sébastien C, Bertuzzi Margherita, Figge Marc Thilo

机构信息

Research Group Applied Systems Biology, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, Jena, Germany.

Faculty of Biological Sciences, Friedrich Schiller University Jena, Jena, Germany.

出版信息

Commun Biol. 2024 Dec 4;7(1):1615. doi: 10.1038/s42003-024-07302-2.

Abstract

The human lung is confronted daily with thousands of microbial invaders reaching the lower respiratory tract. An efficient response by the resident type 1 and type 2 alveolar epithelial cells (AECs) and alveolar macrophages (AMs) cells during the early hours of innate immunity is a prerequisite to maintain a non-inflammatory state, but foremost to rapidly remove harmful substances. One such human-pathogenic invader is the opportunistic fungus Aspergillus fumigatus. If the spherical conidia are not cleared in time, they swell reaching approximately twice of their initial size and germinate to develop hyphae around six hours post-infection. This process of morphological change is crucial as it enables the pathogen to invade the alveolar epithelium and to reach the bloodstream, but also makes it conspicuous for the immune system. During this process, conidia are first in contact with AECs then with migrating AMs, both attempting to internalize and clear the fungus. However, the relative contribution of AMs and AECs to uptake of A. fumigatus remains an open question, especially the capabilities of the barely investigated type 1 AECs. In this study, we present a bottom-up modeling approach to incorporate experimental data on the dynamic increase of the conidial diameter and A. fumigatus uptake by AECs and AMs in a hybrid agent-based model (hABM) for the to-scale simulation of virtual infection scenarios in the human alveolus. By screening a wide range of parameters, we found that type 1 AECs, which cover approximately 95% of the alveolar surface, are likely to have a greater impact on uptake than type 2 AECs. Moreover, the majority of infection scenarios across the regime of tested parameters were cleared through uptake by AMs, whereas the contribution to conidial uptake by AECs was observed to be limited, indicating that their crucial support might mostly consist in mediating chemokine secretion for AM recruitment. Regardless, as the first host cell being confronted with A. fumigatus conidia, our results evidence the large potential impact of type 1 AECs antimicrobial activities, underlining the requirement of increasing experimental efforts on this alveolar constituent.

摘要

人类肺部每天都会遭遇成千上万到达下呼吸道的微生物入侵者。在先天免疫的最初几个小时内,驻留的1型和2型肺泡上皮细胞(AEC)以及肺泡巨噬细胞(AM)做出有效反应,是维持非炎症状态的前提条件,但最重要的是能迅速清除有害物质。烟曲霉就是这样一种人类致病入侵者。如果球形分生孢子没有及时清除,它们会膨胀到初始大小的两倍左右,并在感染后约6小时发芽形成菌丝。这种形态变化过程至关重要,因为它使病原体能够侵入肺泡上皮并进入血液,但同时也使其容易被免疫系统察觉。在此过程中,分生孢子首先与AEC接触,然后与迁移的AM接触,两者都试图内化并清除真菌。然而,AM和AEC对烟曲霉摄取的相对贡献仍是一个悬而未决的问题,尤其是几乎未被研究的1型AEC的能力。在本研究中,我们提出了一种自下而上的建模方法,将关于分生孢子直径动态增加以及AEC和AM对烟曲霉摄取的实验数据纳入基于混合智能体的模型(hABM),以对人类肺泡中的虚拟感染场景进行全尺寸模拟。通过筛选广泛的参数,我们发现覆盖约95%肺泡表面的1型AEC可能比2型AEC对摄取有更大影响。此外,在所测试参数范围内的大多数感染场景是通过AM的摄取清除的,而观察到AEC对分生孢子摄取的贡献有限,这表明它们的关键支持可能主要在于介导趋化因子分泌以招募AM。无论如何,作为第一个接触烟曲霉分生孢子的宿主细胞,我们的结果证明了1型AEC抗菌活性的巨大潜在影响,强调了增加对这种肺泡成分实验研究力度的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d73/11618450/83994d7684ab/42003_2024_7302_Fig1_HTML.jpg

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