A map of signaling responses in the human airway epithelium.

Cell systems Pub Date : 2024-04-17 Epub Date: 2024-03-19 DOI:10.1016/j.cels.2024.02.005
Katherine B McCauley, Kalki Kukreja, Alfredo E Tovar Walker, Aron B Jaffe, Allon M Klein
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Abstract

Receptor-mediated signaling plays a central role in tissue regeneration, and it is dysregulated in disease. Here, we build a signaling-response map for a model regenerative human tissue: the airway epithelium. We analyzed the effect of 17 receptor-mediated signaling pathways on organotypic cultures to determine changes in abundance and phenotype of epithelial cell types. This map recapitulates the gamut of known airway epithelial signaling responses to these pathways. It defines convergent states induced by multiple ligands and diverse, ligand-specific responses in basal cell and secretory cell metaplasia. We show that loss of canonical differentiation induced by multiple pathways is associated with cell-cycle arrest, but that arrest is not sufficient to block differentiation. Using the signaling-response map, we show that a TGFB1-mediated response underlies specific aberrant cells found in multiple lung diseases and identify interferon responses in COVID-19 patient samples. Thus, we offer a framework enabling systematic evaluation of tissue signaling responses. A record of this paper's transparent peer review process is included in the supplemental information.

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人类气道上皮细胞信号反应图。
受体介导的信号在组织再生中起着核心作用,而在疾病中则会失调。在这里,我们为一种再生人体组织模型--气道上皮--建立了信号反应图谱。我们分析了 17 种受体介导的信号通路对器官型培养物的影响,以确定上皮细胞类型的丰度和表型变化。该图谱再现了已知气道上皮细胞对这些通路的信号反应。它定义了多种配体诱导的趋同状态,以及基底细胞和分泌细胞增生过程中配体特异性的各种反应。我们的研究表明,多种途径诱导的典型分化丧失与细胞周期停滞有关,但细胞周期停滞并不足以阻止分化。利用信号-反应图谱,我们表明 TGFB1 介导的反应是多种肺部疾病中发现的特定异常细胞的基础,并确定了 COVID-19 患者样本中的干扰素反应。因此,我们提供了一个能够系统评估组织信号反应的框架。这篇论文的同行评审过程非常透明,相关记录见补充信息。
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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