Sex-dependent effects of maternal high-fat diet during lactation in the offspring of adult THY-Tau22 mice

Thibaut Gauvrit, Hamza Benderradji, Alexandre Pelletier, Kévin Carvalho, Soulaimane Aboulouard, Emilie Faivre, Estelle Chatelain, Hugo Cannafarina, Léna Labous, Agathe Launay, Marie Fourcot, Dimitri Kwiatkowski, Léna Chesnais, Emmanuelle Vallez, Tristan Cardon, Aude Deleau, Bryan Thiroux, Sabiha Eddarkaoui, Anna Bogdanova, Mélanie Besegher, Fabien Delahaye, Jean-Sébastien Annicotte, Stéphanie Le Gras, Anne Tailleux, Michel Salzet, Guillemette Marot, Luc Buée, David Blum, Didier Vieau

Brain

https://doi.org/10.1093/brain/awaf417

Abstract

The perinatal environment has been suggested to participate in the development of tauopathies and Alzheimer’s disease but the molecular and cellular mechanisms involved remain contradictory and under-investigated. Here, we evaluated the effects of a maternal high-fat diet (HFD) during lactation on the development of tauopathy in the THY-Tau22 mouse strain, a model of progressive tau pathology associated with cognitive decline.

During lactation, dams were fed either a chow diet (13.6% of fat) or a HFD (58% of fat). At weaning, offspring were fed a chow diet until sacrifice at 4 months of age (the onset of tau pathology) or 7 months of age (the onset of cognitive impairment).

During lactation, maternal HFD increased body weight gain in offspring. At 3 months of age, maternal HFD led to a mild glucose intolerance only in male offspring. Moreover, it impaired spatial memory in both male and female 6-month-old offspring, with males being more impacted. These cognitive deficits were associated with increased phosphorylation of hippocampal tau protein-observed at 4 months in males and at 7 months in females, highlighting a sex-specific temporal shift. Additionally, maternal HFD modified adult hippocampal neurogenesis (AHN), leading to an increase of mature neuronal cells number in females and of dendritic arborization length in males. Synaptic analysis further revealed that maternal HFD led to synaptic loss only in males. Finally, multi-omics approaches showed that maternal HFD has long-term consequences on both transcriptome, proteome and regulome, this effect being also sex-dependent with mitochondrial pathways, ribosomal activity, cilium and the extracellular matrix predominantly impacted in males, while gliogenesis, myelination and synaptic plasticity were primarily affected in females. Regulome analysis suggested that this sex-dependent phenotype was more related to a temporal shift rather than distinct sex-specific alterations. Collectively, our data suggest that maternal HFD accelerates the development of tauopathy in THY-Tau22 offspring, with sex-dependent effects, males being impacted earlier than females. These findings highlight that exposure to maternal HFD represents a critical window of vulnerability, and potentially of opportunity, for interventions aimed at preventing the development of neurodegenerative diseases.