Placental endocrine function shapes cerebellar development and social behavior

Nat Neurosci. 2021 Oct;24(10):1392-1401. doi: 10.1038/s41593-021-00896-4. Epub 2021 Aug 16.

Abstract

Compromised placental function or premature loss has been linked to diverse neurodevelopmental disorders. Here we show that placenta allopregnanolone (ALLO), a progesterone-derived GABA-A receptor (GABAAR) modulator, reduction alters neurodevelopment in a sex-linked manner. A new conditional mouse model, in which the gene encoding ALLO's synthetic enzyme (akr1c14) is specifically deleted in trophoblasts, directly demonstrated that placental ALLO insufficiency led to cerebellar white matter abnormalities that correlated with autistic-like behavior only in male offspring. A single injection of ALLO or muscimol, a GABAAR agonist, during late gestation abolished these alterations. Comparison of male and female human preterm infant cerebellum also showed sex-linked myelination marker alteration, suggesting similarities between mouse placental ALLO insufficiency and human preterm brain development. This study reveals a new role for a placental hormone in shaping brain regions and behaviors in a sex-linked manner. Placental hormone replacement might offer novel therapeutic opportunities to prevent later neurobehavioral disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Reductase / genetics
  • Animals
  • Autism Spectrum Disorder / etiology
  • Cerebellum / growth & development*
  • Cerebellum / physiology
  • Endocrine Glands / physiology*
  • Female
  • GABA Agonists / pharmacology
  • GABA Modulators
  • Gene Deletion
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mice
  • Muscimol / pharmacology
  • Placenta / physiology*
  • Pregnancy
  • Pregnanolone / deficiency*
  • Pregnanolone / physiology*
  • Receptors, GABA-A / physiology
  • Sex Characteristics
  • Social Behavior*
  • Trophoblasts / metabolism
  • White Matter / pathology

Substances

  • GABA Agonists
  • GABA Modulators
  • Receptors, GABA-A
  • Muscimol
  • Pregnanolone
  • Aldehyde Reductase
  • aldo-keto reductase family 1, member C14 protein, mouse