Analysis of ��-Catenin Signalling Activity Suggests Differential Regulation of Ontogenetically Distinct Dentate Granule Neuron Populations.

Charlotte Billmann, Iris Sch��ffner, Jana Heppt, D Chichung Lie
Author Information
  1. Charlotte Billmann: Institute for Anatomy, Friedrich-Alexander Universit��t Erlangen-N��rnberg, Erlangen, Germany.
  2. Iris Sch��ffner: Institute for Anatomy, Friedrich-Alexander Universit��t Erlangen-N��rnberg, Erlangen, Germany.
  3. Jana Heppt: Institute for Biochemistry, Friedrich-Alexander Universit��t Erlangen-N��rnberg, Erlangen, Germany.
  4. D Chichung Lie: Institute for Anatomy, Friedrich-Alexander Universit��t Erlangen-N��rnberg, Erlangen, Germany. ORCID

Abstract

In mammals, the dentate gyrus of the hippocampus is one of the few regions where neurogenesis continues throughout life. As a result, the dentate gyrus harbours neurons of ontogenetically different origin. Notably, ontogenetically different dentate granule neurons (DGNs) are morphologically distinct and fulfil specialized functions in hippocampal information processing and plasticity. Development of adult-born DGNs is tightly controlled by signals released by the complex cellular environment of the adult dentate gyrus. In mice, an adult-like cytoarchitecture of the dentate gyrus is observed only after postnatal Week���2. The question therefore arises when the signalling environment controlling adult neurogenesis is established and whether development of ontogenetically distinct DGNs is subject to the same regulatory pathways. Here, we analyse BATGAL reporter mice to determine the temporal development of ��-catenin-signalling activity in the murine DGN lineage. We show that the ��-catenin-signalling pattern, which is essential for precise dendritogenesis and neuronal maturation in adulthood, emerges only around 2���weeks after birth and continues to be refined over the next weeks. These results indicate that the signalling environment controlling adult neurogenesis is only gradually established and suggest that the development of ontogenetically distinct DGNs is controlled by different mechanisms.

Keywords

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Grants

  1. LI 858/9-2/Deutsche Forschungsgemeinschaft
  2. LI 858/11-1/Deutsche Forschungsgemeinschaft
  3. 270949263/DFG GRK2162/1/Deutsche Forschungsgemeinschaft

MeSH Term

Animals
Dentate Gyrus
beta Catenin
Mice
Neurons
Neurogenesis
Signal Transduction
Mice, Transgenic
Mice, Inbred C57BL
Animals, Newborn
Gene Expression Regulation, Developmental

Chemicals

beta Catenin

Word Cloud

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