ABCF1 Regulates dsDNA-induced Immune Responses in Human Airway Epithelial Cells.

Front Cell Infect Microbiol

Division of Respirology, Department of Medicine, Firestone Institute for Respiratory Health, McMaster University, Hamilton, ON, Canada.

Published: June 2021

AI Article Synopsis

  • - The airway epithelium plays a vital role in defending against respiratory viral infections, which cause over 2.5 million deaths annually, relying on receptors like TLRs and NLRP to activate immune responses.
  • - ABCF1, a special type of ABC transporter found in the human airway epithelium, acts as a cytosolic nucleic acid sensor that influences the production of important antiviral signals like CXCL10 and interferon-β.
  • - Research confirmed the presence of ABCF1 in human lung tissues and its role in enhancing antiviral responses, indicating its significance in TLR signaling and suggesting that it has a broader role in innate immunity beyond just detecting viral DNA.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525020PMC
http://dx.doi.org/10.3389/fcimb.2020.00487DOI Listing

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