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Dusp8 affects hippocampal size and behavior in mice and humans

Authors :
Martin Heni
Annette Feuchtinger
Oana V. Amarie
Annemarie Zimprich
Peter Baumann
Axel Walch
Matthias H. Tschöp
Sonja C. Schriever
Wolfgang Wurst
Andreas Peter
Valerie Gailus-Durner
Martin Hrabě de Angelis
Helmut Fuchs
Stephanie Kullmann
Sabine M. Hölter
Paul T. Pfluger
Source :
Sci. Rep. 9:19483 (2019), Scientific reports 9(1), 19483 (2019). doi:10.1038/s41598-019-55527-7, Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019), Scientific Reports
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

Dual-specificity phosphatase 8 (Dusp8) acts as physiological inhibitor for the MAPKs Jnk, Erk and p38 which are involved in regulating multiple CNS processes. While Dusp8 expression levels are high in limbic areas such as the hippocampus, the functional role of Dusp8 in hippocampus morphology, MAPK-signaling, neurogenesis and apoptosis as well as in behavior are still unclear. It is of particular interest whether human carriers of a DUSP8 allelic variant show similar hippocampal alterations to mice. Addressing these questions using Dusp8 WT and KO mouse littermates, we found that KOs suffered from mildly impaired spatial learning, increased locomotor activity and elevated anxiety. Cell proliferation, apoptosis and p38 and Jnk phosphorylation were unaffected, but phospho-Erk levels were higher in hippocampi of the KOs. Consistent with a decreased hippocampus size in Dusp8 KO mice, we found reduced volumes of the hippocampal subregions subiculum and CA4 in humans carrying the DUSP8 allelic variant SNP rs2334499:C > T. Overall, aberrations in morphology and behavior in Dusp8 KO mice and a decrease in hippocampal volume of SNP rs2334499:C > T carriers point to a novel, translationally relevant role of Dusp8 in hippocampus function that warrants further studies on the role of Dusp8 within the limbic network.

Details

ISSN :
20452322
Volume :
9
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....7d7e527649b82b72162c2b5cb44529e6
Full Text :
https://doi.org/10.1038/s41598-019-55527-7