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Tytuł pozycji:

The Presynaptic Scaffold Protein Bassoon in Forebrain Excitatory Neurons Mediates Hippocampal Circuit Maturation: Potential Involvement of TrkB Signalling.

Tytuł:
The Presynaptic Scaffold Protein Bassoon in Forebrain Excitatory Neurons Mediates Hippocampal Circuit Maturation: Potential Involvement of TrkB Signalling.
Autorzy:
Annamneedi A; Institute of Biology, Otto-Von-Guericke University, 39120 Magdeburg, Germany.; Center for Behavioral Brain Sciences (CBBS), 39120 Magdeburg, Germany.; Leibniz Institute for Neurobiology (LIN), RG Neuroplasticity, 39118 Magdeburg, Germany.
Del Angel M; Institute of Biology, Otto-Von-Guericke University, 39120 Magdeburg, Germany.
Gundelfinger ED; Center for Behavioral Brain Sciences (CBBS), 39120 Magdeburg, Germany.; Leibniz Institute for Neurobiology (LIN), RG Neuroplasticity, 39118 Magdeburg, Germany.; Institute of Pharmacology & Toxicology, Medical Faculty, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Stork O; Institute of Biology, Otto-Von-Guericke University, 39120 Magdeburg, Germany.; Center for Behavioral Brain Sciences (CBBS), 39120 Magdeburg, Germany.
Çalışkan G; Institute of Biology, Otto-Von-Guericke University, 39120 Magdeburg, Germany.; Center for Behavioral Brain Sciences (CBBS), 39120 Magdeburg, Germany.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jul 26; Vol. 22 (15). Date of Electronic Publication: 2021 Jul 26.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Signal Transduction*
Synaptic Transmission*
Hippocampus/*metabolism
Membrane Glycoproteins/*metabolism
Nerve Tissue Proteins/*metabolism
Prosencephalon/*metabolism
Protein-Tyrosine Kinases/*metabolism
Animals ; Membrane Glycoproteins/genetics ; Mice ; Mice, Knockout ; Nerve Tissue Proteins/genetics ; Protein-Tyrosine Kinases/genetics
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Grant Information:
DFG-CRC 779 Deutsche Forschungsgemeinschaft; ZS/2016/04/78113 Center for Behavioural Brain Sciences-CBBS promoted by Europäische Fonds für regionale Entwicklung-EFRE; SAS-2015-LIN-LWC CBBS-ScienceCampus funded by the Leibniz Association; DFG-RTG2413 Deutsche Forschungsgemeinschaft
Contributed Indexing:
Keywords: TrkB; bassoon; fEPSP; glutamatergic presynapse; hippocampus; neurogenesis
Substance Nomenclature:
0 (Bsn protein, mouse)
0 (Membrane Glycoproteins)
0 (Nerve Tissue Proteins)
EC 2.7.10.1 (Ntrk2 protein, mouse)
EC 2.7.10.1 (Protein-Tyrosine Kinases)
Entry Date(s):
Date Created: 20210807 Date Completed: 20210909 Latest Revision: 20210909
Update Code:
20240105
PubMed Central ID:
PMC8347324
DOI:
10.3390/ijms22157944
PMID:
34360710
Czasopismo naukowe
A presynaptic active zone organizer protein Bassoon orchestrates numerous important functions at the presynaptic active zone. We previously showed that the absence of Bassoon exclusively in forebrain glutamatergic presynapses ( Bsn Emx1 cKO) in mice leads to developmental disturbances in dentate gyrus (DG) affecting synaptic excitability, morphology, neurogenesis and related behaviour during adulthood. Here, we demonstrate that hyperexcitability of the medial perforant path-to-DG (MPP-DG) pathway in Bsn Emx1 cKO mice emerges during adolescence and is sustained during adulthood. We further provide evidence for a potential involvement of tropomyosin-related kinase B (TrkB), the high-affinity receptor for brain-derived neurotrophic factor (BDNF), mediated signalling. We detect elevated TrkB protein levels in the dorsal DG of adult mice (~3-5 months-old) but not in adolescent (~4-5 weeks-old) mice. Electrophysiological analysis reveals increased field-excitatory-postsynaptic-potentials (fEPSPs) in the DG of the adult, but not in adolescent Bsn Emx1 cKO mice. In line with an increased TrkB expression during adulthood in Bsn Emx1 cKO, blockade of TrkB normalizes the increased synaptic excitability in the DG during adulthood, while no such effect was observed in adolescence. Accordingly, neurogenesis, which has previously been found to be increased in adult Bsn Emx1 cKO mice, was unaffected at adolescent age. Our results suggest that Bassoon plays a crucial role in the TrkB-dependent postnatal maturation of the hippocampus.
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