Journal article

Antibacterial Capacity of Differentiated Murine Embryonic Stem Cells During Defined In Vitro Inflammatory Conditions


Authors listFinkensieper, Andreas; Bekhite, Mohamed M.; Fischer, Heike; Nitza, Saskia; Figulla, Hans-R.; Mueller, Joerg P.; Sauer, Heinrich; Wartenberg, Maria

Publication year2013

Pages1977-1990

JournalStem Cells and Development

Volume number22

Issue number14

ISSN1547-3287

eISSN1557-8534

DOI Linkhttps://doi.org/10.1089/scd.2012.0528

PublisherMary Ann Liebert


Abstract
Embryonic stem (ES) cells are a powerful model for the development of cells responsible for the cellular immune response. Therefore, we analyzed the defense and phagocytic capacity of embryoid bodies (EBs) derived from ES cells using in the vitro inflammatory conditions caused by Escherichia coli. Further, we used this phagocytic activity to purify activated immune cells. Our data show that spontaneously differentiated 18-day-old EBs of the cell line CGR8 contained immune cells, which were positive for CD45, CD68, CD11b, F4/80, and CD19. Exposure of these EBs to E. coli with defined infection doses of bacterial colony-forming units (CFUs) led to a significant time-dependent reduction of CFUs, indicating the immune responses exerted by EBs. This was paralleled by an upregulation of inflammatory cytokines, that is, IL-1 beta and TNF-alpha. Western blot analysis of infected EBs indicated an upregulation of CD14 and cytochrome b-245 heavy chain (NOX2). Silencing of NOX2 significantly reduced the antibacterial capacity of EBs, which was partially explained by reduction of F4/80-positive cells. To identify, isolate, and further cultivate phagocytic active cells from differentiated EBs, a co-cultivation assay of differentiated ES cells with green fluorescent protein (GFP)-labeled E. coli was established. Colocalization of GFP-labeled E. coli with cells positive for CD45, CD68, and F4/80 revealed time-dependent phagocytotic uptake, which was underlined by colocalization with the LysoTracker-Red (R) dye as well as pre-incubation with cytochalasin D. In conclusion, a primitive immune response with efficient phagocytosis was responsible for the antibacterial capacity of differentiated EBs.



Citation Styles

Harvard Citation styleFinkensieper, A., Bekhite, M., Fischer, H., Nitza, S., Figulla, H., Mueller, J., et al. (2013) Antibacterial Capacity of Differentiated Murine Embryonic Stem Cells During Defined In Vitro Inflammatory Conditions, Stem Cells and Development, 22(14), pp. 1977-1990. https://doi.org/10.1089/scd.2012.0528

APA Citation styleFinkensieper, A., Bekhite, M., Fischer, H., Nitza, S., Figulla, H., Mueller, J., Sauer, H., & Wartenberg, M. (2013). Antibacterial Capacity of Differentiated Murine Embryonic Stem Cells During Defined In Vitro Inflammatory Conditions. Stem Cells and Development. 22(14), 1977-1990. https://doi.org/10.1089/scd.2012.0528



Keywords


vasculogenesis

Last updated on 2025-02-04 at 02:26