Quantitative analysis of proteome modulations in alveolar epithelial type II cells in response to pulmonary aspergillus fumigatus infection

• Verfasst von: Seddigh, Pegah [VerfasserIn]
• Verfasst von: Poschet, Gernot [VerfasserIn]
• Verfasst von: Opitz, Christiane [VerfasserIn]
• Titel: Quantitative analysis of proteome modulations in alveolar epithelial type II cells in response to pulmonary aspergillus fumigatus infection
• Verf.angabe: Pegah Seddigh, Thilo Bracht, Válerie Molinier-Frenkel, Flavia Castellano, Olaf Kniemeyer, Marc Schuster, Juliane Weski, Anja Hasenberg, Andreas Kraus, Gernot Poschet, Thomas Hager, Dirk Theegarten, Christiane A. Opitz, Axel A. Brakhage, Barbara Sitek, Mike Hasenberg, and Matthias Gunzer
• Umfang: 15 S.
• Fussnoten: Published online December 8, 2017 ; Gesehen ohne PDF am 22.06.2018
• Titel Quelle: Enthalten in: Molecular & cellular proteomics
• Jahr Quelle: 2017
• Band/Heft Quelle: 16(2017), 12, S. 2184-2198
• ISSN Quelle: 1535-9484
• DOI: doi:10.1074/mcp.RA117.000072
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1576784223

Abstract

The ubiquitous mold Aspergillus fumigatus threatens immunosuppressed patients as inducer of lethal invasive aspergillosis. A. fumigatus conidia are airborne and reach the alveoli, where they encounter alveolar epithelial cells (AEC). Previous studies reported the importance of the surfactant-producing AEC II during A. fumigatus infection via in vitro experiments using cell lines. We established a negative isolation protocol yielding untouched primary murine AEC II with a purity >90%, allowing ex vivo analyses of the cells, which encountered the mold in vivo. By label-free proteome analysis of AEC II isolated from mice 24h after A. fumigatus or mock infection we quantified 2256 proteins and found 154 proteins to be significantly differentially abundant between both groups (ANOVA p value ≤ 0.01, ratio of means ≥1.5 or ≤0.67, quantified with ≥2 peptides). Most of these proteins were higher abundant in the infected condition and reflected a comprehensive activation of AECII on interaction with A. fumigatus. This was especially represented by proteins related to oxidative phosphorylation, hence energy production. However, the most strongly induced protein was the l-amino acid oxidase (LAAO) Interleukin 4 induced 1 (IL4I1) with a 42.9 fold higher abundance (ANOVA p value 2.91−10). IL4I1 has previously been found in B cells, macrophages, dendritic cells and rare neurons. Increased IL4I1 abundance in AEC II was confirmed by qPCR, Western blot and immunohistology. Furthermore, A. fumigatus infected lungs showed high levels of IL4I1 metabolic products. Importantly, higher IL4I1 abundance was also confirmed in lung tissue from human aspergilloma. Because LAAO are key enzymes for bactericidal product generation, AEC II might actively participate in pathogen defense. We provide insights into proteome changes of primary AEC II thereby opening new avenues to analyze the molecular changes of this central lung cell on infectious threats. Data are available via ProteomeXchange with identifier PXD005834.