Dusp8 affects hippocampal size and behavior in mice and humans.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
20 12 2019
20 12 2019
Historique:
received:
21
06
2019
accepted:
30
11
2019
entrez:
22
12
2019
pubmed:
22
12
2019
medline:
11
11
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 31862894
doi: 10.1038/s41598-019-55527-7
pii: 10.1038/s41598-019-55527-7
pmc: PMC6925303
doi:
Substances chimiques
p38 Mitogen-Activated Protein Kinases
EC 2.7.11.24
DUSP8 protein, mouse
EC 3.1.3.16
Dual-Specificity Phosphatases
EC 3.1.3.48
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
19483Références
Neuroimage. 2015 Jul 15;115:117-37
pubmed: 25936807
Neuroscience. 2013 Sep 26;249:21-30
pubmed: 23727507
Nature. 2009 Dec 17;462(7275):868-74
pubmed: 20016592
Cell Signal. 2012 Mar;24(3):664-76
pubmed: 22100391
Nat Neurosci. 2012 Dec;15(12):1613-20
pubmed: 23187693
Nature. 2014 Apr 3;508(7494):88-92
pubmed: 24572357
Genome Biol. 2002 Jun 26;3(7):REVIEWS3009
pubmed: 12184814
J Neurosci. 2014 Jan 8;34(2):586-95
pubmed: 24403157
Curr Pharm Des. 2007;13(18):1875-86
pubmed: 17584114
Neuropsychopharmacology. 2019 Jan;44(1):200-213
pubmed: 30214058
Physiol Rev. 2012 Apr;92(2):689-737
pubmed: 22535895
Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):5064-8
pubmed: 15051876
Cell Signal. 2013 Feb;25(2):429-38
pubmed: 23159405
Curr Protoc Mouse Biol. 2015 Dec 02;5(4):331-358
pubmed: 26629775
Biochem J. 2009 Mar 15;418(3):475-89
pubmed: 19228121
J Mol Neurosci. 2011 Mar;43(3):376-90
pubmed: 20878262
Circ Res. 2016 Jul 8;119(2):249-60
pubmed: 27225478
Behav Brain Res. 2018 Oct 15;352:8-22
pubmed: 28927717
Nat Genet. 2012 Sep;44(9):981-90
pubmed: 22885922
J Biol Chem. 1996 Nov 1;271(44):27205-8
pubmed: 8910287
Neuroinformatics. 2016 Jul;14(3):339-51
pubmed: 27075850
Curr Protoc Mouse Biol. 2015 Dec 02;5(4):291-309
pubmed: 26629773
Neuron. 2013 Mar 6;77(5):955-68
pubmed: 23473324
Microbiol Mol Biol Rev. 2016 Jul 27;80(3):793-835
pubmed: 27466283
Brain Res. 2012 Oct 2;1476:58-70
pubmed: 22541166
Mol Psychiatry. 2018 Feb;23(2):487
pubmed: 28194007
Neuroimage. 2007 Oct 15;38(1):95-113
pubmed: 17761438
J Neurosci. 2000 Apr 15;20(8):2964-77
pubmed: 10751449
J Neurochem. 1995 Oct;65(4):1823-33
pubmed: 7561881
J Clin Invest. 2017 Jan 3;127(1):24-32
pubmed: 28045396