Placenta and early-life programming
A further central topic in the laboratory focuses on the molecular and physiological pathways through which the placenta mediates early-life programming. Our central hypothesis sustains that endogenous hormonal and nutrient environments in utero, as well as placental adaptations to maternal stress or nutritional imbalance, shape the offspring’s later susceptibility to psychiatric conditions. Using placenta-specific knockout/knockdown techniques and multi-level analysis of placental and central pathways in disease programming in mice and humans, combined with murine behavioral approaches, we ultimately aim to identify biomarkers and therapeutic windows for early prevention of psychiatric disorders rooted in fetal development.