Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, University of Utah Spencer Fox Eccles School of Medicine, Salt Lake City, UT.
George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, UT.
J Immunol. 2024 Sep 1;213(5):600-611. doi: 10.4049/jimmunol.2300325.
The aryl hydrocarbon receptor (AHR) is a receptor/transcription factor widely expressed in the lung. The physiological roles of AHR expressed in the alveolar epithelium remain unclear. In this study, we tested the hypothesis that alveolar epithelial AHR activity plays an important role in modulating inflammatory responses and maintaining alveolar integrity during lung injury and repair. AHR is expressed in alveolar epithelial cells (AECs) and is active. AHR activation with the endogenous AHR ligand, FICZ (5,11-dihydroindolo[3,2-b] carbazole-6-carboxaldehyde), significantly suppressed inflammatory cytokine expression in response to inflammatory stimuli in primary murine AECs and in the MLE-15 epithelial cell line. In an LPS model of acute lung injury in mice, coadministration of FICZ with LPS suppressed protein leak, reduced neutrophil accumulation in BAL fluid, and suppressed inflammatory cytokine expression in lung tissue and BAL fluid. Relevant to healing following inflammatory injury, AHR activation suppressed TGF-β-induced expression of genes associated with epithelial-mesenchymal transition. Knockdown of AHR in primary AECs with shRNA or in CRISPR-Cas-9-induced MLE-15 cells resulted in upregulation of α-smooth muscle actin (αSma), Col1a1, and Fn1 and reduced expression of epithelial genes Col4a1 and Sdc1. MLE-15 clones lacking AHR demonstrated accelerated wound closure in a scratch model. AHR activation with FICZ enhanced barrier function (transepithelial electrical resistance) in primary murine AECs and limited decline of transepithelial electrical resistance following inflammatory injury. AHR activation in AECs preserves alveolar integrity by modulating inflammatory cytokine expression while enhancing barrier function and limiting stress-induced expression of mesenchymal genes.
芳香烃受体 (AHR) 是一种广泛表达于肺部的受体/转录因子。肺泡上皮细胞中表达的 AHR 的生理作用尚不清楚。在这项研究中,我们检验了一个假设,即肺泡上皮细胞 AHR 活性在调节肺部损伤和修复期间的炎症反应和维持肺泡完整性方面发挥着重要作用。AHR 在肺泡上皮细胞 (AEC) 中表达并具有活性。用内源性 AHR 配体 FICZ(5,11-二氢吲哚并[3,2-b]咔唑-6-甲醛)激活 AHR,可显著抑制原代小鼠 AEC 和 MLE-15 上皮细胞系中炎症刺激物引起的炎症细胞因子表达。在 LPS 诱导的急性肺损伤小鼠模型中,FICZ 与 LPS 共同给药可抑制蛋白渗漏,减少 BAL 液中的中性粒细胞积聚,并抑制肺组织和 BAL 液中的炎症细胞因子表达。与炎症损伤后的愈合相关,AHR 激活可抑制 TGF-β诱导的上皮-间充质转化相关基因的表达。用 shRNA 或 CRISPR-Cas-9 诱导的 MLE-15 细胞中的 AHR 敲低导致α-平滑肌肌动蛋白 (αSma)、Col1a1 和 Fn1 的上调以及上皮基因 Col4a1 和 Sdc1 的表达减少。缺乏 AHR 的 MLE-15 克隆在划痕模型中表现出更快的伤口闭合。用 FICZ 激活 AHR 可增强原代小鼠 AEC 的屏障功能(上皮电阻),并限制炎症损伤后上皮电阻的下降。AHR 在 AEC 中的激活通过调节炎症细胞因子的表达来维持肺泡完整性,同时增强屏障功能并限制应激诱导的间充质基因的表达。