New functions of Semaphorin 3E and its receptor PlexinD1 during developing and adult hippocampal formation View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2018-12

AUTHORS

Agata Mata, Vanessa Gil, Jeús Pérez-Clausell, Miguel Dasilva, Mari Carmen González-Calixto, Eduardo Soriano, José Manuel García-Verdugo, Maria V. Sanchez-Vives, José Antonio del Río

ABSTRACT

The development and maturation of cortical circuits relies on the coordinated actions of long and short range axonal guidance cues. In this regard, the class 3 semaphorins and their receptors have been seen to be involved in the development and maturation of the hippocampal connections. However, although the role of most of their family members have been described, very few data about the participation of Semaphorin 3E (Sema3E) and its receptor PlexinD1 during the development and maturation of the entorhino-hippocampal (EH) connection are available. In the present study, we focused on determining their roles both during development and in adulthood. We determined a relevant role for Sema3E/PlexinD1 in the layer-specific development of the EH connection. Indeed, mice lacking Sema3E/PlexinD1 signalling showed aberrant layering of entorhinal axons in the hippocampus during embryonic and perinatal stages. In addition, absence of Sema3E/PlexinD1 signalling results in further changes in postnatal and adult hippocampal formation, such as numerous misrouted ectopic mossy fibers. More relevantly, we describe how subgranular cells express PlexinD1 and how the absence of Sema3E induces a dysregulation of the proliferation of dentate gyrus progenitors leading to the presence of ectopic cells in the molecular layer. Lastly, Sema3E mutant mice displayed increased network excitability both in the dentate gyrus and the hippocampus proper. More... »

PAGES

1381

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41598-018-19794-0

DOI

http://dx.doi.org/10.1038/s41598-018-19794-0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1100427066

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29358640


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