LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: Transcriptomic comparison of primary human lung cells with lung tissue samples and the human A549 lung cell line highlights cell type specific responses during infections with influenza A virus

    Wilhelm Bertrams / Katja Hönzke / Benedikt Obermayer / Mario Tönnies / Torsten T. Bauer / Paul Schneider / Jens Neudecker / Jens C. Rückert / Thorsten Stiewe / Andrea Nist / Stephan Eggeling / Norbert Suttorp / Thorsten Wolff / Stefan Hippenstiel / Bernd Schmeck / Andreas C. Hocke

    Scientific Reports, Vol 12, Iss 1, Pp 1-

    2022  Volume 11

    Abstract: Abstract Influenza A virus (IAV) causes pandemics and annual epidemics of severe respiratory infections. A better understanding of the molecular regulation in tissue and cells upon IAV infection is needed to thoroughly understand pathogenesis. We ... ...

    Abstract Abstract Influenza A virus (IAV) causes pandemics and annual epidemics of severe respiratory infections. A better understanding of the molecular regulation in tissue and cells upon IAV infection is needed to thoroughly understand pathogenesis. We analyzed IAV replication and gene expression induced by IAV strain H3N2 Panama in isolated primary human alveolar epithelial type II cells (AECIIs), the permanent A549 adenocarcinoma cell line, alveolar macrophages (AMs) and explanted human lung tissue by bulk RNA sequencing. Primary AECII exhibit in comparison to AM a broad set of strongly induced genes related to RIG-I and interferon (IFN) signaling. The response of AECII was partly mirrored in A549 cells. In human lung tissue, we observed induction of genes unlike in isolated cells. Viral RNA was used to correlate host cell gene expression changes with viral burden. While relative induction of key genes was similar, gene abundance was highest in AECII cells and AM, while weaker in the human lung (due to less IAV replication) and A549 cells (pointing to their limited suitability as a model). Correlation of host gene induction with viral burden allows a better understanding of the cell-type specific induction of pathways and a possible role of cellular crosstalk requiring intact tissue.
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2022-11-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  2. Article ; Online: Human alveolar progenitors generate dual lineage bronchioalveolar organoids

    Karen Hoffmann / Benedikt Obermayer / Katja Hönzke / Diana Fatykhova / Zeynep Demir / Anna Löwa / Luiz Gustavo Teixeira Alves / Emanuel Wyler / Elena Lopez-Rodriguez / Maren Mieth / Morris Baumgardt / Judith Hoppe / Theresa C. Firsching / Mario Tönnies / Torsten T. Bauer / Stephan Eggeling / Hong-Linh Tran / Paul Schneider / Jens Neudecker /
    Jens C. Rückert / Achim D. Gruber / Matthias Ochs / Markus Landthaler / Dieter Beule / Norbert Suttorp / Stefan Hippenstiel / Andreas C. Hocke / Mirjana Kessler

    Communications Biology, Vol 5, Iss 1, Pp 1-

    2022  Volume 17

    Abstract: The GSK3 inhibitor CHIR99021 is required to maintain the alveolar lineage in alveolar progenitors grown in airway media or AT2 cells become plastic, with the observed effects acting outside of its role as a GSK3B inhibitor. ...

    Abstract The GSK3 inhibitor CHIR99021 is required to maintain the alveolar lineage in alveolar progenitors grown in airway media or AT2 cells become plastic, with the observed effects acting outside of its role as a GSK3B inhibitor.
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2022-08-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article ; Online: Pneumolysin induced mitochondrial dysfunction leads to release of mitochondrial DNA

    Andreas Nerlich / Maren Mieth / Eleftheria Letsiou / Diana Fatykhova / Katja Zscheppang / Aki Imai-Matsushima / Thomas F. Meyer / Lisa Paasch / Timothy J. Mitchell / Mario Tönnies / Torsten T. Bauer / Paul Schneider / Jens Neudecker / Jens C. Rückert / Stephan Eggeling / Maria Schimek / Martin Witzenrath / Norbert Suttorp / Stefan Hippenstiel /
    Andreas C. Hocke

    Scientific Reports, Vol 8, Iss 1, Pp 1-

    2018  Volume 13

    Abstract: Abstract Streptococcus pneumoniae (S.pn.) is the most common bacterial pathogen causing community acquired pneumonia. The pore-forming toxin pneumolysin (PLY) is the major virulence factor of S.pn. and supposed to affect alveolar epithelial cells thereby ...

    Abstract Abstract Streptococcus pneumoniae (S.pn.) is the most common bacterial pathogen causing community acquired pneumonia. The pore-forming toxin pneumolysin (PLY) is the major virulence factor of S.pn. and supposed to affect alveolar epithelial cells thereby activating the immune system by liberation of danger-associated molecular patterns (DAMP). To test this hypothesis, we established a novel live-cell imaging based assay to analyse mitochondrial function and associated release of mitochondrial DNA (mtDNA) as DAMP in real-time. We first revealed that bacterially released PLY caused significant changes of the cellular ATP homeostasis and led to morphologic alterations of mitochondria in human alveolar epithelial cells in vitro and, by use of spectral live-tissue imaging, in human alveoli. This was accompanied by strong mitochondrial calcium influx and loss of mitochondrial membrane potential resulting in opening of the mitochondrial permeability transition pore and mtDNA release without activation of intrinsic apoptosis. Moreover, our data indicate cellular mtDNA liberation via microvesicles, which may contribute to S.pn. related pro-inflammatory immune activation in the human alveolar compartment.
    Keywords Medicine ; R ; Science ; Q
    Subject code 610
    Language English
    Publishing date 2018-01-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top