Genome-Wide Gene Expression Analysis Reveals Unique Genes Signatures of Epithelial Reorganization in Primary Airway Epithelium Induced by Type-I, -II and -III Interferons

Bibliographic Details
Title: Genome-Wide Gene Expression Analysis Reveals Unique Genes Signatures of Epithelial Reorganization in Primary Airway Epithelium Induced by Type-I, -II and -III Interferons
Authors: Anna Erb, Ulrich M. Zissler, Madlen Oelsner, Adam M. Chaker, Carsten B. Schmidt-Weber, Constanze A. Jakwerth
Source: Biosensors, Vol 12, Iss 11, p 929 (2022)
Publisher Information: MDPI AG, 2022.
Publication Year: 2022
Collection: LCC:Biotechnology
Subject Terms: microarray, gene expression analysis, airway epithelial, type-I, -II and -III Interferons, epithelial integrity, Biotechnology, TP248.13-248.65
More Details: Biosensors such as toll-like receptors (TLR) induce the expression of interferons (IFNs) after viral infection that are critical to the first step in cell-intrinsic host defense mechanisms. Their differential influence on epithelial integrity genes, however, remains elusive. A genome-wide gene expression biosensor chip for gene expression sensing was used to examine the effects of type-I, -II, and -III IFN stimulation on the epithelial expression profiles of primary organotypic 3D air-liquid interface airway cultures. All types of IFNs induced similar interferon-stimulated genes (ISGs): OAS1, OAS2, and IFIT2. However, they differentially induced transcription factors, epithelial modulators, and pro-inflammatory genes. Type-I IFN-induced genes were associated with cell–cell adhesion and tight junctions, while type-III IFNs promoted genes important for transepithelial transport. In contrast, type-II IFN stimulated proliferation-triggering genes associated and enhanced pro-inflammatory mediator secretion. In conclusion, with our microarray system, we provide evidence that the three IFN types exceed their antiviral ISG-response by inducing distinct remodeling processes, thereby likely strengthening the epithelial airway barrier by enhancing cross-cell-integrity (I), transepithelial transport (III) and finally reconstruction through proliferation (II).
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2079-6374
Relation: https://www.mdpi.com/2079-6374/12/11/929; https://doaj.org/toc/2079-6374
DOI: 10.3390/bios12110929
Access URL: https://doaj.org/article/347b9773ae1e4dd7b3c47cbc93dafea7
Accession Number: edsdoj.347b9773ae1e4dd7b3c47cbc93dafea7
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:20796374
DOI:10.3390/bios12110929
Published in:Biosensors
Language:English