van Doeselaar, L.* ; Abromeit, A.* ; Stark, T.* ; Menegaz, D.* ; Ballmann, M.* ; Mitra, S.* ; Yang, H.* ; Rehawi, G.* ; Huettl, R.E.* ; Bordes, J.* ; Narayan, S.* ; Harbich, D.* ; Deussing, J.M.* ; Rammes, G.* ; Czisch, M.* ; Knauer-Arloth, J. ; Eder, M.* ; Lopez, J.P.* ; Schmidt, M.V.*
FKBP51 in glutamatergic forebrain neurons promotes early life stress inoculation in female mice.
Nat. Commun. 16:2529 (2025)
Early life stress (ELS) can increase vulnerability to psychiatric disorders, but also trigger resilience. FKBP51 has been associated with an increased risk for developing psychiatric disorders, specifically in interaction with ELS exposure. Here, the contribution of FKBP51 in glutamatergic forebrain neurons to the long-term consequences of ELS was investigated in both sexes. In female wild-type Fkbp5lox/lox mice, ELS exposure led to an anxiolytic phenotype and improved memory performance in a stressful context, however this ELS effect was absent in Fkbp5Nex mice. These interactive FKBP51 x ELS effects in female mice were also reflected in reduced brain region volumes, and on structural and electrophysiological properties of CA1 pyramidal neurons of the dorsal hippocampus. In contrast, the behavioral, structural and functional effects in male ELS mice were less pronounced and independent of FKBP51. RNA sequencing of the hippocampus revealed the transcription factor 4 (TCF4) as a potential regulator of the female interactive effects. Cre-dependent viral overexpression of TCF4 in female Nex-Cre mice led to similar beneficial effects on behavior as the ELS exposure. This study demonstrates a sex-specific role for FKBP51 in mediating the adaptive effects of ELS on emotional regulation, cognition, and neuronal function, implicating TCF4 as a downstream effector.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Typ der Hochschulschrift
Herausgeber
Schlagwörter
Major Depressive Disorder; Gene-environment Interactions; Lasting Consequences; Hippocampal Volume; Cognitive Function; Brain; Vulnerability; Plasticity; Glucocorticoids; Responsiveness
Keywords plus
Sprache
englisch
Veröffentlichungsjahr
2025
Prepublished im Jahr
0
HGF-Berichtsjahr
2025
ISSN (print) / ISBN
2041-1723
e-ISSN
2041-1723
ISBN
Bandtitel
Konferenztitel
Konferzenzdatum
Konferenzort
Konferenzband
Quellenangaben
Band: 16,
Heft: 1,
Seiten: ,
Artikelnummer: 2529
Supplement: ,
Reihe
Verlag
Nature Publishing Group
Verlagsort
London
Tag d. mündl. Prüfung
0000-00-00
Betreuer
Gutachter
Prüfer
Topic
Hochschule
Hochschulort
Fakultät
Veröffentlichungsdatum
0000-00-00
Anmeldedatum
0000-00-00
Anmelder/Inhaber
weitere Inhaber
Anmeldeland
Priorität
Begutachtungsstatus
Peer reviewed
POF Topic(s)
30205 - Bioengineering and Digital Health
Forschungsfeld(er)
Enabling and Novel Technologies
PSP-Element(e)
G-503800-001
Förderungen
German Research Foundation (DFG)
Deutsche Forschungsgemeinschaft (German Research Foundation)
Copyright
Erfassungsdatum
2025-05-08