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Projekt Druckansicht

Structure-function relationships of the VILlP-1 - a4ß2 nAChR interaction - implications for nicotine-induced functional up-regulation of the a4ß2 nicotinic acetylcholine receptor

Fachliche Zuordnung Biologische Psychiatrie
Förderung Förderung von 2006 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 24839276
 
Erstellungsjahr 2015

Zusammenfassung der Projektergebnisse

In in vitro and in vivo studies, we demonstrated that Aβ-treatment has potent detrimental effects on the profile and longevity of hippocampal LTP. The VILIP-1-derived L27 peptide enhances LTP and can rescue from detrimental Aβ effects on LTP. Both effects are phospholipid and nAChR-dependent (MLA and Annexin). Since VILIP-1-KO +/- show reduced LTP, and the detrimental Aβ effect is enhanced in VILIP-1-KO with lowered VILIP- 1 levels confirms a role of VILIP-1 in synaptic plasticity and memory. Thus, if Aβ, nicotinic receptors, VILIP-1 and synaptic plasticity are linked, then the VILIP-1-mimetic L27 peptide may serve as a therapeutic peptide.

Projektbezogene Publikationen (Auswahl)

  • (2011) Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. Transl. Psychiatry 1
    Braunewell KH, Dwary A D, Richter F, Trappe K, Zhao C, Giegling I, Schönrath K and D. Rujescu
    (Siehe online unter https://doi.org/10.1038/tp.2011.20)
  • (2012). The visinin-like proteins VILIP-1 and VILIP-3 in Alzheimer's disease-old wine in new bottles. Front. Mol. Neurosci. 5:20
    Braunewell KH
    (Siehe online unter https://doi.org/10.3389/fnmol.2012.00020)
  • (2014) Regulation of hippocampal synaptic plasticity thresholds and changes in exploratory and learning behavior in dominant negative NPR-B mutant rats, Frontiers Mol Neurosci. 7:95
    Barmashenko G, Buttgereit J, Zcelik C, Herring N, Bader M, Manahan-Vaughan D, Braunewell KH
    (Siehe online unter https://doi.org/10.3389/fnmol.2014.00095)
 
 

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