Division of Respirology, Department of Medicine, Firestone Institute for Respiratory Health, McMaster University, Hamilton, ON, Canada.
Department of Biology, University of Waterloo, Waterloo, ON, Canada.
Front Cell Infect Microbiol. 2020 Sep 16;10:487. doi: 10.3389/fcimb.2020.00487. eCollection 2020.
The airway epithelium represents a critical component of the human lung that helps orchestrate defenses against respiratory tract viral infections, which are responsible for more than 2.5 million deaths/year globally. Innate immune activities of the airway epithelium rely on Toll-like receptors (TLRs), nucleotide binding and leucine-rich-repeat pyrin domain containing (NLRP) receptors, and cytosolic nucleic acid sensors. ATP Binding Cassette (ABC) transporters are ubiquitous across all three domains of life-Archaea, Bacteria, and Eukarya-and expressed in the human airway epithelium. ABCF1, a unique ABC family member that lacks a transmembrane domain, has been defined as a cytosolic nucleic acid sensor that regulates CXCL10, interferon-β expression, and downstream type I interferon responses. We tested the hypothesis that ABCF1 functions as a dsDNA nucleic acid sensor in human airway epithelial cells important in regulating antiviral responses. Expression and localization experiments were performed using hybridization and immunohistochemistry in human lung tissue, while confirmatory transcript and protein expression was performed in human airway epithelial cells. Functional experiments were performed with siRNA methods in a human airway epithelial cell line. Complementary transcriptomic analyses were performed to explore the contributions of ABCF1 to gene expression patterns. Using archived human lung and human airway epithelial cells, we confirm expression of ABCF1 gene and protein expression in these tissue samples, with a role for mediating CXCL10 production in response to dsDNA viral mimic challenge. Although, ABCF1 knockdown was associated with an attenuation of select genes involved in the antiviral responses, Gene Ontology analyses revealed a greater interaction of ABCF1 with TLR signaling suggesting a multifactorial role for ABCF1 in innate immunity in human airway epithelial cells. ABCF1 is a candidate cytosolic nucleic acid sensor and modulator of TLR signaling that is expressed at gene and protein levels in human airway epithelial cells. The precise level where ABCF1 protein functions to modulate immune responses to pathogens remains to be determined but is anticipated to involve IRF-3 and CXCL10 production.
气道上皮细胞是人体肺部的一个重要组成部分,有助于协调针对呼吸道病毒感染的防御机制,而这些感染每年在全球范围内导致超过 250 万人死亡。气道上皮细胞的先天免疫活动依赖于 Toll 样受体 (TLR)、核苷酸结合和富含亮氨酸重复吡咯啉域包含 (NLRP) 受体以及细胞质核酸传感器。ATP 结合盒 (ABC) 转运蛋白存在于所有三个生命领域——古菌、细菌和真核生物中,并在人类气道上皮细胞中表达。ABCF1 是一种独特的 ABC 家族成员,缺乏跨膜结构域,已被定义为细胞质核酸传感器,可调节 CXCL10、干扰素-β表达和下游 I 型干扰素反应。我们测试了假设,即 ABCF1 作为人类气道上皮细胞中重要的 dsDNA 核酸传感器发挥作用,调节抗病毒反应。使用杂交和免疫组织化学在人肺组织中进行表达和定位实验,同时在人气道上皮细胞中进行确认的转录和蛋白表达实验。在人气道上皮细胞系中使用 siRNA 方法进行功能实验。进行互补转录组学分析以探讨 ABCF1 对基因表达模式的贡献。使用存档的人类肺和人气道上皮细胞,我们在这些组织样本中证实了 ABCF1 基因和蛋白表达,其在 dsDNA 病毒模拟物刺激下介导 CXCL10 产生的作用。尽管 ABCF1 敲低与参与抗病毒反应的一些基因的衰减有关,但基因本体论分析显示 ABCF1 与 TLR 信号转导的相互作用更大,这表明 ABCF1 在人类气道上皮细胞的先天免疫中具有多因素作用。ABCF1 是一种候选的细胞质核酸传感器和 TLR 信号转导调节剂,在人气道上皮细胞中以基因和蛋白水平表达。ABCF1 蛋白调节对病原体免疫反应的确切水平仍有待确定,但预计涉及 IRF-3 和 CXCL10 产生。