Prenatal exposure to maternal stress drives neurodevelopmental disruptions in the fetal hypothalamus
- 1University of British Columbia
Abstract
The hypothalamus plays a central role in integrating physiological stressors to maintain homeostasis, yet how fetal neurodevelopment in the hypothalamus is shaped by intrauterine maternal stress exposure remains understudied. This is especially true in the context of sex-divergent mechanisms underlying neurodevelopmental disorders (NDDs), which are increasingly being linked to perturbation of the intrauterine environment. Herein, we utilize a mouse model of prenatal maternal cold stress exposure to study the impacts on neural stem and progenitor cell (NSPC) developmental programs in the fetal hypothalamus. Pregnant mice were exposed to cold stress from embryonic day 11.5 (E11.5) to E15.5 and fetal hypothalamic NSPCs from both male and female embryos were analyzed. Exposure to maternal stress altered fetal hypothalamic neurodevelopment, increasing TUJ1+ neuron number in males, while enhancing neuronal dendritic arborization in females. To define underlying molecular changes, we performed single-cell RNA sequencing of hypothalamic NSPCs. Interestingly, we identified distinct baseline transcriptional profiles between male and female NSPCs. In females, maternal stress upregulated pathways related to GABAergic differentiation and neuronal projection morphogenesis, with these alterations being maintained across more differentiated neuronal populations. Ligand-receptor analysis further indicated that maternal stress alters cell-cell communication within NSPCs, predominantly in females. Together, these findings demonstrate that prenatal maternal stress alters hypothalamic NSPC developmental programs uniquely in each sex, and suggest that disrupted intercellular signaling may contribute to underlying sex differences in social behaviors previously reported for this model (Rosin et al., 2021).
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BibTeX
@misc{bao2026prenatal,
title = {{Prenatal exposure to maternal stress drives neurodevelopmental disruptions in the fetal hypothalamus}},
author = {K. Bao and M. Rosin and J. M. Rosin},
howpublished = {bioRxiv},
year = {2026},
month = jun,
doi = {10.64898/2026.06.08.730949},
url = {https://www.biorxiv.org/content/10.64898/2026.06.08.730949v2},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Prenatal exposure to maternal stress drives neurodevelopmental disruptions in the fetal hypothalamus
AU - K. Bao
AU - M. Rosin
AU - J. M. Rosin
PY - 2026
DA - 2026/06/08
PB - bioRxiv
DO - 10.64898/2026.06.08.730949
UR - https://www.biorxiv.org/content/10.64898/2026.06.08.730949v2
AB - The hypothalamus plays a central role in integrating physiological stressors to maintain homeostasis, yet how fetal neurodevelopment in the hypothalamus is shaped by intrauterine maternal stress exposure remains understudied. This is especially true in the context of sex-divergent mechanisms underlying neurodevelopmental disorders (NDDs), which are increasingly being linked to perturbation of the intrauterine environment. Herein, we utilize a mouse model of prenatal maternal cold stress exposure to study the impacts on neural stem and progenitor cell (NSPC) developmental programs in the fetal hypothalamus. Pregnant mice were exposed to cold stress from embryonic day 11.5 (E11.5) to E15.5 and fetal hypothalamic NSPCs from both male and female embryos were analyzed. Exposure to maternal stress altered fetal hypothalamic neurodevelopment, increasing TUJ1+ neuron number in males, while enhancing neuronal dendritic arborization in females. To define underlying molecular changes, we performed single-cell RNA sequencing of hypothalamic NSPCs. Interestingly, we identified distinct baseline transcriptional profiles between male and female NSPCs. In females, maternal stress upregulated pathways related to GABAergic differentiation and neuronal projection morphogenesis, with these alterations being maintained across more differentiated neuronal populations. Ligand-receptor analysis further indicated that maternal stress alters cell-cell communication within NSPCs, predominantly in females. Together, these findings demonstrate that prenatal maternal stress alters hypothalamic NSPC developmental programs uniquely in each sex, and suggest that disrupted intercellular signaling may contribute to underlying sex differences in social behaviors previously reported for this model (Rosin et al., 2021).
ER -