A Knockout of the IFITM3 Gene Increases the Sensitivity of WI-38 VA13 Cells to the Influenza A Virus.
Natalya EshchenkoMariia V SergeevaEvgenii ZhuravlevKira S KudriaElena GoncharovaAndrey B KomissarovGrigory A StepanovPublished in: International journal of molecular sciences (2024)
One of the ways to regulate the sensitivity of human cells to the influenza virus is to knock out genes of the innate immune response. Promising targets for the knockout are genes of the interferon-inducible transmembrane protein (IFITM) family, in particular the IFITM3 gene, whose product limits the entry of a virus into the cell by blocking the fusion of the viral and endosomal membranes. In this study, by means of genome-editing system CRISPR/Cas9, monoclonal cell lines with an IFITM3 knockout were obtained based on WI-38 VA13 cells (human origin). It was found that such cell lines are more sensitive to infection by influenza A viruses of various subtypes. Nevertheless, this feature is not accompanied by an increased titer of newly formed viral particles in a culture medium.
Keyphrases
- crispr cas
- genome editing
- immune response
- induced apoptosis
- genome wide
- genome wide identification
- cell cycle arrest
- sars cov
- endothelial cells
- copy number
- dendritic cells
- machine learning
- genome wide analysis
- oxidative stress
- deep learning
- stem cells
- single cell
- cell death
- signaling pathway
- amino acid
- induced pluripotent stem cells
- mesenchymal stem cells
- small molecule
- genetic diversity
- cell proliferation
- pluripotent stem cells