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    Novel protocol for the in vitro cultivation and Magnetic-activated cell sorting (MACS) of highly purified neonatal murine microglia and astrocytes (2020)

    Art
    Poster
    Autoren
    Zelenka, Laura (WE 7)
    Pägelow, Dennis (WE 7)
    Krüger, Christina
    Seele, Jana
    van Vorst, Kira (WE 7)
    Ebner, Frederike (WE 6)
    Rausch, Sebastian (WE 6)
    Hartmann, Susanne (WE 6)
    Lehnardt, Seija
    Fulde, Marcus (WE 7)
    Kongress
    Zoonoses 2020 - International Symposium on Zoonoses Research
    online, 15. – 16.10.2020
    Quelle
    Zoonoses 2020 – International Symposium on Zoonoses Research : online meeting; joint meeting of the German Research Platform for Zoonoses and the Research Network of Zoonotic Diseases : October 15th - 16th, 2020 : program and abstracts — [National Research Platform for Zoonoses and the Research Network of Zoonotic Infectious Diseases] (Hrsg.)
    Berlin, 2020 — S. Beitrag ID:317
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://evis.events/event/119/contributions/2454/contribution.pdf
    Kontakt
    Institut für Immunologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51834
    immunologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Konferenzband: https://www.openagrar.de/receive/openagrar_mods_00065483
    Abstract: https://evis.events/event/119/contributions/2454/contribution.pdf

    Infectious diseases of the central nervous system (CNS) are of major health concern with high mortality rates and frequent occurrence of convalescence, occasionally also including long-term sequelae. The crosstalk and reactivity of the cell type glia, especially microglia and astrocytes, have progressively gathered research attention in understanding proper brain function and defense to viral as well as bacterial infections. In this study, we modified previously established techniques by applying an optimized Magnetic-activated cell sorting (MACS) protocol using CD11b and ACSA-2 labeled MicroBeads for the isolation of microglia and astrocytes from neonatal mouse brains. Thereby, we achieved highly viable and pure (~99 %) microglia and astrocytes as confirmed by FACS analysis. By using this developed method, highly purified primary microglia and astrocytes, potentially with different genetic backgrounds, can be cultivated in vitro. This will facilitate the analysis of the cell-type specific involvement in the frame of CNS diseases by applying this highly useful quick and easy tool in future approaches.