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Projekt Druckansicht

Pathogenese erblicher Neuropathien: Implicationen von Komponenten des angeborenen und adaptiven Immunsystems

Fachliche Zuordnung Klinische Neurologie; Neurochirurgie und Neuroradiologie
Förderung Förderung von 2013 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 227548520
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

In summary, we can support our leading hypothesis that Schwann cell borne PDGF-A (and/or PDGF-B) might function as the initially unknown “activator 1” for inducing CSF-1 in peripheral nerves of CMT1 models. Conditional inactivation of PDGF-A specifically in Schwann cells led to a reduced expression of CSF-1, accompanied by a reduction of pathogenic macrophages and improved axonal preservation in Cx32def mice. It will be exciting also to decipher the role of the PDGF-B isoform in this context, as our corresponding in vitro experiments would predict a similar function.

Projektbezogene Publikationen (Auswahl)

  • 2018. Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration. EMBO J. 37
    Shashi, V., M.M. Magiera, D. Klein, .... R. Martini, C. Janke, and J. Senderek
    (Siehe online unter https://doi.org/10.15252/embj.2018100540)
  • 2018. Macrophage Depletion Ameliorates Peripheral Neuropathy in Aging Mice. The Journal of Neuroscience 38:4610-4620
    Yuan, X., D. Klein, S. Kerscher, B.L. West, J. Weis, I. Katona, and R. Martini
    (Siehe online unter https://doi.org/10.1523/JNEUROSCI.3030-17.2018)
  • 2018. Targeting myelin lipid metabolism as a potential therapeutic strategy in a model of CMT1A neuropathy. Nat Commun. 9:3025
    Fledrich, R., T. Abdelaal, L. Rasch, V. Bansal, V. Schutza, B. Brugger, C. Luchtenborg, T. Prukop, J. Stenzel, R.U. Rahman, D. Hermes, D. Ewers, W. Mobius, T. Ruhwedel, I. Katona, J. Weis, D. Klein, R. Martini, W. Bruck, W.C. Muller, S. Bonn, I. Bechmann, K.A. Nave, R.M. Stassart, and M.W. Sereda
    (Siehe online unter https://doi.org/10.1038/s41467-018-05420-0)
  • 2018. Translational Science of Rare Diseases – From Rare to Care III, Tutzing, Germany: “Early onset targeting of macrophages ameliorates neuropathic changes in a mouse model for Charcot-Marie-Tooth 1A disease”
    D. Klein, J. Groh, X. Yuan, B.L. West, and R. Martini
  • 2019. Current Topics in Myelin Research, Kassel, Germany: “Physical Exercise as a possible Therapy for CMT1X”
    D. Klein, X. Yuan, J. Groh, and R. Martini
  • 2019. Targeting microglia attenuates neuroinflammation-related neural damage in mice carrying human PLP1 mutations. Glia. 67:277-290
    Groh, J., D. Klein, K. Berve, B.L. West, and R. Martini
    (Siehe online unter https://doi.org/10.1002/glia.23539)
 
 

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