| Literature DB >> 27707798 |
Dolores Irala1, Antonela Bonafina1, Paula Aldana Fontanet1, Fernando Cruz Alsina1, Gustavo Paratcha1, Fernanda Ledda2.
Abstract
The formation of synaptic connections during nervous system development requires the precise control of dendrite growth and synapse formation. Although glial cell line-derived neurotrophic factor (GDNF) and its receptor GFRα1 are expressed in the forebrain, the role of this system in the hippocampus remains unclear. Here, we investigated the consequences of GFRα1 deficiency for the development of hippocampal connections. Analysis of conditional Gfra1 knockout mice shows a reduction in dendritic length and complexity, as well as a decrease in postsynaptic density specializations and in the synaptic localization of postsynaptic proteins in hippocampal neurons. Gain- and loss-of-function assays demonstrate that the GDNF-GFRα1 complex promotes dendritic growth and postsynaptic differentiation in cultured hippocampal neurons. Finally, in vitro assays revealed that GDNF-GFRα1-induced dendrite growth and spine formation are mediated by NCAM signaling. Taken together, our results indicate that the GDNF-GFRα1 complex is essential for proper hippocampal circuit development.Entities:
Keywords: Dendrite complexity; Dendritic spines; GDNF; Hippocampus; Mouse; NCAM; Rat; Structural plasticity
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Year: 2016 PMID: 27707798 DOI: 10.1242/dev.140350
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868