Published November 23, 2021 | Version v1

Developmental decrease of entorhinal-hippocampal communication in immune-challenged DISC1 knockdown mice

  • 1. Institute of Developmental Neurophysiology, Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany

Description

The prefrontal-hippocampal dysfunction that underlies cognitive deficits in mental disorders emerges during early development. The lateral entorhinal cortex (LEC) is tightly interconnected with both prefrontal cortex (PFC) and hippocampus (HP), yet its contribution to the early dysfunction is fully unknown. Here we show that mice that mimic the dual genetic (G) -environmental (E) etiology (GE mice) of psychiatric risk have poor LEC-dependent recognition memory at pre-juvenile age and abnormal communication within LEC-HP-PFC networks throughout development. These functional and behavioral deficits relate to sparser projections from LEC to CA1 and decreased efficiency of axonal terminals to activate the hippocampal circuits in neonatal GE mice. In contrast, the direct entorhinal drive to PFC is not affected, yet the PFC is indirectly compromised, as target of the under-activated HP. Thus, the entorhinal-hippocampal circuit is already impaired from neonatal age on in GE mice.

Notes

We thank Dr. Joseph Gogos for providing the DISC1 mice and Dr. Simon Wiegert for providing AAV9-CaMKII-eOPN3-mScarlet. We also thank A. Marquardt, C. Tietze, A. Dahlmann, and P. Putthoff for excellent technical assistance. This work was funded by grants from the European Research Council (ERC-2015-CoG 681577 to I.L.H.-O.), the German Research Foundation (SFB 936 B5 and Ha4466/11-1 to I.L.H.-O.), Marie Curie Training Network euSNN (MSCA-ITN-H2020-860563 to I.L.H.-O.), Horizon 2020 DEEPER 101016787 (to I.L.H.-O.), and Landesforschungsförderung Hamburg (LFF76, LFF73 to I.L.H.-O.).

Files

Xu et al. - 2021 - Developmental decrease of entorhinal-hippocampal c.pdf

Additional details

Related works

Is identical to
10.1038/s41467-021-27114-w (DOI)

Funding

European Commission
PSYCHOCELL - Cellular substrate of abnormal network maturation in neuropsychiatric disorders 681577
European Commission
euSNN - European School of Network Neuroscience 860563
European Commission
DEEPER - DEEP BRAIN PHOTONIC TOOLS FOR CELL-TYPE SPECIFIC TARGETING OF NEURAL DISEASES 101016787