Die Rolle des IL-1 Signalwegs in der Regulation von Entwicklung und Funktion der Mikroglia

• Antragsteller: Professor Dr. Ari Waisman
• Fachliche Zuordnung: Molekulare und zelluläre Neurologie und Neuropathologie ; Immunologie
• Förderung: Förderung von 2016 bis 2019
• Projektkennung: Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 317624411

• Erstellungsjahr: 2021

Zusammenfassung der Projektergebnisse

Microglia are brain macrophages that emerge early during embryogenesis. These cells seed the brain, and proliferate until they have formed a grid-like distribution in the central nervous system (CNS) that is maintained throughout lifespan. Using genetic methods, we could show that the precursors of these cells are within the CNS: we showed that if we ablate microglia, the cells that come instead of them and populate the CNS originate from the CNS and not the bone marrow. Importantly, we found that the cytokine interleukin-1 (IL-1), plays an important role in this process. Using similar techniques, we could further show that expression of the receptor for IL-1, termed IL-1R1 by microglia cells is not critical for their function during autoimmune brain inflammation, when using a mouse model of multiple sclerosis. In another set of experiments, we could show that the one cell type where IL-1 signaling does play a role and is critical for the development of CNS autoimmunity, are the endothelial cells of the blood brain barrier. Our data show that although IL-1 signaling is important for the expansion of microglia in the CNS, it is not critical for their function during autoimmunity of the CNS but rather it is important for the integrity of the blood brain barrier.

Projektbezogene Publikationen (Auswahl)

• (2018) Antigen-presenting cell diversity for T cell reactivation in central nervous system autoimmunity. J Mol Med (Berl). 96(12):1279-1292
  Waisman A, Johann L
  (Siehe online unter https://doi.org/10.1007/s00109-018-1709-7)
• (2019) Novel Microglia Depletion Systems: A Genetic Approach Utilizing Conditional Diphtheria Toxin Receptor Expression and a Pharmacological Model Based on the Blocking of Macrophage Colony-Stimulating Factor 1 Receptor. Methods Mol Biol. 2034:217-230
  Kitic M, See P, Bruttger J, Ginhoux F, Waisman A.
  (Siehe online unter https://doi.org/10.1007/978-1-4939-9658-2_16)
• (2019) Unraveling the T-B tangle in anti-CD20 multiple sclerosis therapy. Proc Natl Acad Sci USA. 116(51):25376-25377
  Waisman A, Ebering A.
  (Siehe online unter https://doi.org/10.1073/pnas.1919044116)
• (2020) Microglial A20 Protects the Brain from CD8 T-Cell-Mediated Immunopathology. Cell Rep. 30(5):1585-1597
  Mohebiany AN, Ramphal NS, Karram K, Di Liberto G, Novkovic T, Klein M, Marini F, Kreutzfeldt M, Härtner F, Lacher SM, Bopp T, Mittmann T, Merkler D, Waisman A
  (Siehe online unter https://doi.org/10.1016/j.celrep.2019.12.097)